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US20040182600A1 - Method for growing carbon nanotubes, and electronic device having structure of ohmic connection to carbon element cylindrical structure body and production method thereof - Google Patents

Method for growing carbon nanotubes, and electronic device having structure of ohmic connection to carbon element cylindrical structure body and production method thereof Download PDF

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Publication number
US20040182600A1
US20040182600A1 US10/773,311 US77331104A US2004182600A1 US 20040182600 A1 US20040182600 A1 US 20040182600A1 US 77331104 A US77331104 A US 77331104A US 2004182600 A1 US2004182600 A1 US 2004182600A1
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carbon nanotube
carbon
growing
cylindrical structure
structure body
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US10/773,311
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Akio Kawabata
Mizuhisa Nihei
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Fujitsu Ltd
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Fujitsu Ltd
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Priority claimed from JP2003078353A external-priority patent/JP4401094B2/en
Priority claimed from JP2003083192A external-priority patent/JP4059795B2/en
Application filed by Fujitsu Ltd filed Critical Fujitsu Ltd
Assigned to FUJITSU LIMITED reassignment FUJITSU LIMITED ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: NIHEI, MIZUHISA, KAWABATA, AKIO
Publication of US20040182600A1 publication Critical patent/US20040182600A1/en
Priority to US12/458,308 priority Critical patent/US8163647B2/en
Abandoned legal-status Critical Current

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    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23CCOATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C16/00Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes
    • C23C16/22Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes characterised by the deposition of inorganic material, other than metallic material
    • C23C16/26Deposition of carbon only
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B82NANOTECHNOLOGY
    • B82YSPECIFIC USES OR APPLICATIONS OF NANOSTRUCTURES; MEASUREMENT OR ANALYSIS OF NANOSTRUCTURES; MANUFACTURE OR TREATMENT OF NANOSTRUCTURES
    • B82Y10/00Nanotechnology for information processing, storage or transmission, e.g. quantum computing or single electron logic
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B82NANOTECHNOLOGY
    • B82YSPECIFIC USES OR APPLICATIONS OF NANOSTRUCTURES; MEASUREMENT OR ANALYSIS OF NANOSTRUCTURES; MANUFACTURE OR TREATMENT OF NANOSTRUCTURES
    • B82Y30/00Nanotechnology for materials or surface science, e.g. nanocomposites
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01LSEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
    • H01L21/00Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
    • H01L21/02Manufacture or treatment of semiconductor devices or of parts thereof
    • H01L21/04Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer
    • H01L21/18Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer the devices having semiconductor bodies comprising elements of Group IV of the Periodic Table or AIIIBV compounds with or without impurities, e.g. doping materials
    • H01L21/28Manufacture of electrodes on semiconductor bodies using processes or apparatus not provided for in groups H01L21/20 - H01L21/268
    • H01L21/283Deposition of conductive or insulating materials for electrodes conducting electric current
    • H01L21/285Deposition of conductive or insulating materials for electrodes conducting electric current from a gas or vapour, e.g. condensation
    • H01L21/28506Deposition of conductive or insulating materials for electrodes conducting electric current from a gas or vapour, e.g. condensation of conductive layers
    • H01L21/28512Deposition of conductive or insulating materials for electrodes conducting electric current from a gas or vapour, e.g. condensation of conductive layers on semiconductor bodies comprising elements of Group IV of the Periodic Table
    • H01L21/28556Deposition of conductive or insulating materials for electrodes conducting electric current from a gas or vapour, e.g. condensation of conductive layers on semiconductor bodies comprising elements of Group IV of the Periodic Table by chemical means, e.g. CVD, LPCVD, PECVD, laser CVD
    • H01L21/28562Selective deposition
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01LSEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
    • H01L21/00Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
    • H01L21/70Manufacture or treatment of devices consisting of a plurality of solid state components formed in or on a common substrate or of parts thereof; Manufacture of integrated circuit devices or of parts thereof
    • H01L21/71Manufacture of specific parts of devices defined in group H01L21/70
    • H01L21/768Applying interconnections to be used for carrying current between separate components within a device comprising conductors and dielectrics
    • H01L21/76838Applying interconnections to be used for carrying current between separate components within a device comprising conductors and dielectrics characterised by the formation and the after-treatment of the conductors
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01LSEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
    • H01L21/00Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
    • H01L21/70Manufacture or treatment of devices consisting of a plurality of solid state components formed in or on a common substrate or of parts thereof; Manufacture of integrated circuit devices or of parts thereof
    • H01L21/71Manufacture of specific parts of devices defined in group H01L21/70
    • H01L21/768Applying interconnections to be used for carrying current between separate components within a device comprising conductors and dielectrics
    • H01L21/76838Applying interconnections to be used for carrying current between separate components within a device comprising conductors and dielectrics characterised by the formation and the after-treatment of the conductors
    • H01L21/76877Filling of holes, grooves or trenches, e.g. vias, with conductive material
    • H01L21/76879Filling of holes, grooves or trenches, e.g. vias, with conductive material by selective deposition of conductive material in the vias, e.g. selective C.V.D. on semiconductor material, plating
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01LSEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
    • H01L2221/00Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof covered by H01L21/00
    • H01L2221/10Applying interconnections to be used for carrying current between separate components within a device
    • H01L2221/1068Formation and after-treatment of conductors
    • H01L2221/1094Conducting structures comprising nanotubes or nanowires
    • HELECTRICITY
    • H05ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
    • H05KPRINTED CIRCUITS; CASINGS OR CONSTRUCTIONAL DETAILS OF ELECTRIC APPARATUS; MANUFACTURE OF ASSEMBLAGES OF ELECTRICAL COMPONENTS
    • H05K3/00Apparatus or processes for manufacturing printed circuits
    • H05K3/40Forming printed elements for providing electric connections to or between printed circuits
    • H05K3/4038Through-connections; Vertical interconnect access [VIA] connections
    • H05K3/4076Through-connections; Vertical interconnect access [VIA] connections by thin-film techniques

Definitions

  • the present invention relates to an electronic device having a structure for ohmic connection to a carbon element cylindrical structure body represented by a carbon nanotube and a production method thereof, which techniques are widely applicable when a carbon element cylindrical structure body is applied to an electronic device.
  • the present invention also relates to a method for growing carbon nanotubes.
  • FIG. 1 schematically shows the connection of a carbon element cylindrical structure body 11 , which is formed as a longitudinal via material in a via hole of an electronic device, to a lower wiring Cu layer 13 and an upper wiring Cu layer 15 .
  • a via hole formed in an interlayer insulating film 17 on the lower wiring layer 13 a bundle of carbon element cylindrical structure bodies 11 is formed in vertical orientation.
  • the carbon element cylindrical structure body 11 is grown by using a chemical vapor deposition (CVD) method and, at this time, a catalyst metal (for example, Ni) layer 19 , necessary for the growth of the carbon element cylindrical structure body, is present on the wiring layer exposed in the via hole.
  • a Ti layer 21 is inserted between the carbon element cylindrical structure body 11 and the upper wiring layer 15 .
  • connection between the carbon element cylindrical structure body 11 and the upper wiring layer 15 is an ohmic connection resulting from carbidization (formation into TiC) of the Ti layer 21 intervening therebetween.
  • This method is a technique of contacting the carbon element cylindrical structure body with the Ti layer and then performing a heat treatment at a high temperature to cause TiC formation at the interface, thereby obtaining an ohmic connection (see, Y. Zhang et al., Science 285, 1719 (1999)).
  • JP 9-31757 A discloses a method of producing graphite nanotubes at a low temperature by CVD, where the graphite nanotube is produced at 650 to 800° C.
  • Japanese Unexamined Patent Publication (Kokai) No. 10-203810 JP 10-203810 A describes a technique of growing carbon nanotubes on a substrate at a relatively low temperature, where the growth requires a plasma produced by a direct-current glow discharge.
  • JP 2000-353467 A describes a method for producing a cold cathode device, where a diamond or diamond-like carbon electron-releasing material is formed by hot-filament CVD.
  • the production of carbon nanotubes is not referred to therein.
  • Japanese National Publication (Kohyo) No. 2002-518280 (JP 2002-518280 A) describes a method for growing carbon nanotubes by hot-filament CVD. In this method, an electric field is applied during the growth.
  • the electronic device having a structure of an ohmic connection to a carbon element cylindrical structure body of the present invention can be produced by a method comprising disposing a metal material on a connection objective capable of ohmically contacting with a carbon element cylindrical structure body, and forming a carbon element cylindrical structure body according to chemical vapor deposition using the metal material as the catalyst while accomplishing an ohmic contact between the carbon element cylindrical structure body and the connection objective.
  • a connection objective a material capable of ohmically contacting with a carbon element cylindrical structure body, an ohmic connection structure therebetween can be realized simultaneously with the growth of the carbon element cylindrical structure body.
  • the electronic device having a structure of an ohmic connection to a carbon element cylindrical structure body of the present invention can be produced by a method comprising forming a first stack of a first material capable of ohmically contacting with a carbon element cylindrical structure body and a second material of catalyst metal disposed on the first material, heat-treating the first stack in vacuum or in a hydrogen atmosphere to form a second stack made of a lower layer composed of an alloy of the first material and the second material, an intermediate layer composed of the first material and an upper layer composed of a fine particle formed of the second material, and forming a carbon element cylindrical structure body by chemical vapor deposition using the fine particle of the second material on the surface of the second stack as the catalyst to incorporate the fine particle of the second material into the inside of the carbon element cylindrical structure body and at the same time, connect, by an ohmic contact, the side wall of the carbon element cylindrical structure body to the intermediate layer composed of the first material.
  • carbon element cylindrical structure body is a linear nanostructure constituted by carbon atoms and this is a generic term for a carbon nanotube, a cup-stacked type structure, a carbon fiber or the like.
  • the method for growing a carbon nanotube of the present invention is a method comprising disposing a substrate in a growth chamber, supplying a starting material gas to the chamber and orientation-growing a carbon nanotube on the substrate by CVD, the method being characterized in that neither an electric field nor a plasma is used for the growth of the carbon nanotube and that heat generated from a filament disposed in the growth chamber is utilized.
  • carbon nanotubes can be orientation-grown at a relatively low temperature, specifically, even at a substrate growth face temperature of less than 500° C.
  • FIG. 2A is a schematic view for explaining a first embodiment of the present invention, where a carbon element cylindrical structure body is applied to the longitudinal via of an electronic device;
  • FIG. 2B is an enlarged view of the portion denoted by B in FIG. 2A;
  • FIG. 3A is a view for explaining a laminate film used in the method for producing a structure of an ohmic connection of the present invention
  • FIG. 3B is a view for explaining a NiTi alloy layer obtained from the Ni/Ti laminate film of FIG. 3A;
  • FIG. 4A is a schematic partial enlarged view for explaining the first stack used in a second embodiment of the present invention.
  • FIG. 4B is a schematic partial enlarged view for explaining the second stack used in the second embodiment of the present invention.
  • FIGS. 5A to 5 C are schematic views showing the production process in Example 1;
  • FIGS. 6A and 6B are schematic views showing the production process in Example 2.
  • FIG. 7 is a schematic view for explaining the method for growing carbon nanotubes of the present invention.
  • FIGS. 8A and 8B are views for explaining the growth of carbon nanotubes in Example 3.
  • FIGS. 9A and 9B are views for explaining the growth of carbon nanotubes in Example 4.
  • FIGS. 10A and 10B are views for explaining the growth of carbon nanotubes in Example 5.
  • carbon element cylindrical structure body is a linear nanostructure constituted by carbon atoms and this is a generic term for a carbon nanotube, a cup-stacked type structure, a carbon fiber or the like.
  • the present invention is described by referring to carbon nanotube which is one representative of these nanostructures.
  • a Ti layer is not present between the carbon element cylindrical structure body 11 and the lower wiring layer 13 and therefore, an ohmic contact by the TiC formation cannot be formed. Furthermore, as for the contact with the lower wiring layer 13 , an ohmic contact cannot be formed as in the case of the upper wiring layer 15 by depositing a Ti layer after the growth of the carbon element cylindrical structure body 11 and, subsequently, performing a high-temperature heat treatment. That is, in the conventional structure, an ohmic contact ensuring sufficiently low resistance cannot be formed between the lower wiring layer and the carbon element cylindrical structure body and, thus, the wiring/via part formed by the carbon element cylindrical structure body disadvantageously has high resistance.
  • One of objects of a first aspect of the present invention is to provide an electronic device having a structure of an ohmic connection to a carbon element cylindrical structure body, which can be realized simultaneously with the growth of the carbon element cylindrical structure body, and a production method thereof.
  • FIGS. 2A and 2B schematically show an embodiment in which the present invention is applied to an electronic device having a longitudinal via.
  • a via hole formed in an interlayer insulating film 37 on a lower wiring (Cu) layer 33 a bundle of carbon nanotubes 31 is formed in vertical orientation.
  • a laminate film obtained by previously forming, on the lower wiring layer 33 in the via hole, a Ti layer 45 for the TiC formation of the junction part of the carbon nanotube 31 to the lower wiring layer 33 and forming thereon a catalyst metal (for example, Ni) layer necessary for the growth of nanotubes is used.
  • a catalyst metal for example, Ni
  • the Ni/Ti laminate film is subject to an elevation of the substrate temperature at the time of growing carbon nanotubes by chemical vapor deposition and changes into a NiTi alloy layer 45 a (FIG. 3B).
  • the carbon nanotube 31 grows on the surface of the NiTi alloy layer 45 a by using, as a nucleus, the catalyst metal Ni fine particle in the alloy.
  • FIG. 2B which is an enlarged view of the portion denoted by B in FIG. 2A
  • the Ni fine particle 39 is embraced in the inside at the root of the growing carbon nanotube 31 and the side wall of the nanotube 31 comes into contact with Ti remaining on the surface of the alloy layer 45 a.
  • This contact portion 47 becomes the ohmic contact site where Ti is carbidized.
  • an ohmic contact can be formed between the alloy layer 45 a and the nanotube 31 simultaneously with the growth of carbon nanotube.
  • the carbon nanotube 31 formed within the via hole and the upper wiring layer 35 can be ohmically connected, as in the conventional art, by the carbidization (TiC formation) of the Ti layer 41 intervening therebetween.
  • the carbon nanotube can be connected by a good ohmic contact with both the lower and upper wiring layers 33 and 35 and a via with low resistance can be realized.
  • connection objective to which the carbon nanotube 31 is ohmically connected is an alloy layer 45 a and the metal material thereon is a catalyst metal fine particle 39 .
  • a second embodiment where the present invention is applied to an electronic device having a longitudinal via is described below.
  • a first stack 54 made of a Ti layer 52 for the TiC formation of the junction part of the carbon nanotube to the lower wiring layer 33 and a catalyst metal Ni layer 53 provided thereon is formed on the lower wiring layer 33 within a via hole.
  • This stack is heat-treated in a vacuum or in a hydrogen atmosphere to form a second stack 61 constituted by, as shown in FIG. 4B which is a partial enlarged view similarly to FIG. 2B, a lower layer 55 of TiNi alloy, an intermediate layer 57 of Ti and an upper layer of Ni fine particle 59 .
  • the Ti layer 57 corresponds to the connection objective to which the carbon nanotube is ohmically connected in the first embodiment
  • the Ni fine particle 59 similarly corresponds to the metal material as the catalyst fine particle in the previous case.
  • connection objective to which the carbon element cylindrical structure body is connected by an ohmic contact is the NiTi alloy layer 45 a in the first embodiment and this layer is derived from the Ti layer 45 which is previously formed.
  • the connection objective is the Ti intermediate layer 57 and this layer is also derived from the Ti layer which is previously formed (Ti layer before heat treatment).
  • the connection objective to which the carbon nanotube is connected can be regarded as a Ti layer for carbidization (Ti layer before the heat treatment accompanying the growth of nanotubes (in the first embodiment) or Ti layer formed by the heat treatment before the growth of nanotube (in the second embodiment)), that is, a material of undergoing ohmic connection to the carbon nanotube by carbidization.
  • connection objective Nb, Si or C other than Ti can be used as the material (connection objective) undergoing an ohmic connection to carbon nanotube by carbidization.
  • the material as the connection objective is C (carbon)
  • the carbon nanotube and the connection objective are connected by a carbon-carbon bond and, in the present invention, this connection by a carbon-carbon bond is also called herein connection by carbidization.
  • Fe or Co can be used other than Ni.
  • An alloy containing at least one metal selected from Ni, Fe and Co can also be used.
  • One of objects of a second aspect of the present invention is to provide a novel method capable of producing carbon nanotubes orientation-grown at a low temperature without relying on auxiliary means such as electric field (or plasma) which has been heretofore employed and, thereby, to enable the growth of carbon nanotubes on, for example, a semiconductor circuit which cannot be subjected to a high-temperature treatment.
  • auxiliary means such as electric field (or plasma) which has been heretofore employed
  • a filament disposed in the growth chamber is used as a heat source for the growth of carbon nanotubes by CVD.
  • a filament for heating is known as hot-filament CVD but in conventional techniques of using this method for the growth of carbon nanotubes, a filament temperature of 1,600° C. is required (see, Chemical Physics Letters, 342, pp. 259-264 (2001)).
  • the hot filament generates a heat upon passing of a current.
  • the filament temperature at the growth of carbon nanotubes is preferably 400° C. or more. If the filament temperature is less than 400° C., this is insufficient to supply an energy for decomposing the starting material gas, whereas if it is unnecessarily elevated, the energy is wasted. Therefore, the filament temperature in general is preferably from 400 to 1,000° C., more preferably from 400 to 600° C., still more preferably from 400 to 500° C.
  • the hot-filament should be produced from a material capable of enduring high temperature (400° C. or more) at the growth of carbon nanotubes and at the same time, undergoing no or little chemical reaction with the starting material gas or a decomposition product thereof.
  • the present inventors have found that for the purpose of producing carbon nanotubes by CVD from a starting material gas containing a carbon source, a filament made of rhenium or a material mainly comprising rhenium is suitable.
  • a hot-filament 212 is disposed to face a growth substrate 214 in a vacuum chamber (reaction chamber) 210 to which a starting material gas is supplied.
  • the distance between the filament 212 and the substrate 214 is determined according to the carbon nanotube growth conditions (e.g., the kind of starting material gas used and the growth rate).
  • the hot filament 212 can be moved above the substrate 214 to uniformly grow carbon nanotubes in an arbitrary area.
  • the substrate 214 may be moved by fixing the position of the hot filament 212 .
  • the hot filament 212 and the substrate 214 both may be relatively moved.
  • rotation or reciprocation can be employed.
  • the filament 212 can be made to cause a reciprocating movement in the horizontal direction while moving the substrate 214 in the vertical direction by the movement of a substrate stage 216 .
  • the filament 212 is connected to, for example, an A.C. power source 218 and the substrate stage 216 is generally equipped with substrate heating means (not shown).
  • a carbon source gas containing carbon is used as the starting material for the growth of carbon nanotubes.
  • the carbon source gas may be a hydrocarbon gas such as methane, ethane, acetylene, propane or butane, or a gas of alcohols such as methanol or ethanol.
  • a mixture of two or more carbon sources may also be used.
  • the starting material gas may contain, in addition to the carbon source, one or both of a reactive gas such as hydrogen and an inert gas such as helium or argon.
  • a reactive gas such as hydrogen
  • an inert gas such as helium or argon.
  • the total pressure of the starting material gas in the growth chamber may be approximately from 0.1 to 100 kPa. If the pressure is less than 0.1 kPa, the growth rate of carbon nanotubes decreases, whereas if it exceeds 100 kPa, there may be a danger of the starting material gas leaking out of the growth chamber.
  • the total pressure of the starting material gas is preferably from 0.1 to 10 kPa, more preferably from 0.3 to 10 kPa.
  • a substance acting as the catalyst for the growth reaction must be present on the substrate surface where carbon nanotubes are grown.
  • a transition metal such as Fe, Ni, Co or Pd may be used and an alloy of two or more of these transition metals may also be used.
  • an alloy of such a transition metal capable of acting as the catalyst and a metal of not acting as the catalyst, for example, Fe—Pt and Co—Pt, may also be used.
  • the catalyst may form a thin film on the surface of the growth substrate or may be a fine particle dispersed on the substrate surface.
  • the diameter of the growing carbon nanotube can be controlled by controlling the diameter of the fine particle. For example, as described in Examples later, when fine particle catalysts having diameters of about 7 nm and 4 nm were used, carbon nanotubes having diameters of about 15 nm and 8 nm could be obtained, respectively.
  • the thin-film catalyst may be formed by any method. For example, evaporation or sputtering can be used.
  • the thickness of the thin film can be arbitrarily selected.
  • the fine particle catalyst can be formed by utilizing laser ablation or a solution reaction.
  • impurities such as carbon are sometimes attached to the periphery of the fine particle formed.
  • the impurities are generally evaporated and disappear by heat treatment at a high temperature of 500° C. or more, however, in some cases, the impurities cannot be completely removed by this heat treatment only. In such a case, the remaining impurities can be removed by, for example, an annealing treatment using a reactive gas such as hydrogen.
  • the annealing can be performed under conditions the same as or close to the temperature and pressure conditions at the growth. Therefore, this treatment can be performed in the growth chamber before the growth of carbon nanotubes is started, and, subsequently, the growth of carbon nanotubes can be performed in the same growth chamber.
  • a hot-filament is used, whereby the carbon nanotube can be orientation-grown at a relatively low temperature.
  • a temperature of 600° C. or less of the growth surface of the substrate is sufficient for obtaining carbon nanotubes.
  • the temperature of the growth surface of the substrate may even be less than 500° C.
  • the substrate on which carbon nanotubes are grown for example, a substrate of a semiconductor represented by silicon can be used. As described above, the temperature of the substrate surface can be relatively low and therefore, a substrate material which cannot be used as the substrate for the growth of carbon nanotubes in conventional CVD methods, such as a glass substrate, can also be used.
  • an apparatus where a growth substrate is contained and a starting material gas is supplied to orientation-grow carbon nanotubes on the substrate by CVD and where a hot filament is equipped in the growth chamber, is used.
  • an SiO 2 interlayer insulating film 103 (500 nm) is deposited on a lower wiring Cu layer 101 on a substrate (not shown) and thereon, a resist pattern (not shown) having openings, in the regions at which wiring vias are to be formed, is formed.
  • a wiring via 105 is formed in the interlayer insulating film 103 .
  • a Ti layer (50 nm) and an Ni catalyst metal layer (10 nm) are deposited in this order on the entire surface of the substrate by sputtering or evaporation.
  • a Ti layer 107 (50 nm)/Ni layer 109 (10 nm) laminate film is caused to remain in the wiring via by the lift-off method using the resist film.
  • a layer formed of Fe or Co may be used as the catalyst metal layer or a layer of an alloy containing at least one of Ni, Fe and Co may also be used.
  • a fine particle may be used in place of the thin layer of catalyst metal.
  • an Nb layer, an Si layer or a graphite carbon layer may be used.
  • carbon nanotubes 111 are grown by CVD (see, FIG. 5B).
  • thermal CVD is used.
  • the substrate is placed in a vacuum chamber (reaction chamber) and, for example, a mixed gas of acetylene and hydrogen at flow rates of 80 sccm and 20 sccm, respectively, is introduced as a reaction gas into the vacuum chamber and the pressure and substrate temperature are set to 200 Pa and 900° C., respectively.
  • hot-filament CVD for performing gas dissociation by a hot filament, may be used.
  • a mixed gas of acetylene and hydrogen at flow rates of 80 sccm and 20 sccm, respectively, is introduced as a reaction gas into the vacuum chamber and the pressure, substrate temperature and hot filament temperature are set to 1,000 Pa, 600° C. and 1,800° C., respectively.
  • DC plasma enhanced hot-filament CVD, combining direct-current (DC) plasma and a hot filament may also be used.
  • a mixed gas of acetylene and hydrogen, at flow rates of 80 sccm and 20 sccm, respectively, is introduced as a reaction gas into the vacuum chamber and the pressure, substrate temperature and hot filament temperature are set to 1,000 Pa, 600° C.
  • a direct-current (DC) electric field of ⁇ 400 V was applied to the substrate with respect to the chamber (grounded).
  • the application of direct-current (DC) electric field is advantageous for obtaining perpendicularly oriented carbon nanotubes with respect to the substrate.
  • the carbon nanotubes 111 are grown by taking the Ni fine particle 109 a into the inside at the root from the Ni layer 109 and ohmically connected to the Ti layer 107 through TiC generated by the partial carbidization of Ti in the lower layer 107 .
  • the substrate in the vacuum chamber may be heat-treated (for example, at 600° C. for 30 minutes) in vacuum or in a hydrogen atmosphere to alloy the Ni/Ti laminate film.
  • an Ni fine particle, a Ti layer and an NiTi alloy layer are formed in this order from the film surface.
  • the carbon nanotube 111 is grown by CVD while incorporating the Ni fine particle in the uppermost part as the catalyst metal into the inside of the tube side wall and at the same time, the side wall of the nanotube is joined with the Ti layer 107 a lying beneath.
  • a Ti layer 113 (50 nm) and a Cu layer 115 (500 nm) are deposited in this order by sputtering or evaporation.
  • a heat treatment (for example, 500 to 800° C. for 30 minutes) is performed to cause TiC formation in the upper end of the carbon nanotube 111 .
  • the carbon nanotube 111 was connected by ohmic contact to the upper and lower wiring layers 101 and 115 .
  • an SiO 2 insulating film 123 (500 nm) is deposited on an Si substrate 121 and thereon, a resist pattern (not shown) having openings in the regions, at which electrodes are to be formed, is formed.
  • a Ti layer (50 nm) and an Ni catalyst metal layer (10 nm) are deposited in this order by sputtering or evaporation.
  • a Ti layer 125 (50 nm)/Ni layer 127 (10 nm) laminate film (electrode pattern) in the openings of the resist pattern is caused to remain by the lift-off method using the resist film.
  • a carbon nanotube 129 is grown by CVD (see, FIG. 6B).
  • the CVD and growth conditions used may be the same as those described in Example 1.
  • the Ni/Ti laminate film may be heat-treated in advance of the growth of carbon nanotube by CVD.
  • a direct-current (DC) electric field of 400 V was applied between electrodes.
  • the carbon nanotube 129 is grown by incorporating a part of Ni in the Ni layer 127 as a catalyst element 127 a into the inside and is ohmically connected to the Ti layer 125 through TiC generated by partial carbidization of Ti in the Ti layer 125 .
  • an Ni thin film 222 for catalyst was formed on a silicon substrate 220 by evaporation and, thereon, an SiN insulating film 224 (thickness: 500 nm) having an opening with a diameter of 2 ⁇ m was formed.
  • the thickness of the Ni thin film 222 can be arbitrarily decided, but the thickness was set here to 2 nm.
  • This substrate was introduced into a reaction part (vacuum chamber) (not shown) and the substrate temperature was set to 500° C.
  • a starting material gas prepared by mixing argon and acetylene at a ratio of 80:20 was supplied to the reaction part at a flow rate of 100 ccm and the total gas pressure in the reaction part was adjusted to 1 kPa by the control in an exhaust system connected to a vacuum pump.
  • a hot filament (made of rhenium) was moved above the substrate and with a distance of about 6 mm to the substrate, a current of about 8 A was passed. By this passing of a current, the hot filament temperature was elevated to 800° C. After maintaining this state for 1 minute, the passing of the current to the hot filament was stopped.
  • the remaining starting material gas in the reaction part was vacuum-evacuated and the substrate was taken out from the reaction part.
  • carbon nanotubes 226 having a length of about 2 ⁇ m were formed in the vertical direction from the substrate surface.
  • a film of Fe fine particles 232 having a diameter of 7 nm was formed by laser ablation in an opening with a diameter of 2 ⁇ m of an SiN insulating film 234 (thickness: 500 nm) formed on a silicon substrate 230 .
  • This substrate was introduced into a reaction part and the substrate temperature was set to 400° C.
  • a current of about 0.7 A was passed to a hot filament moved above the substrate and the hot filament temperature was set to about 400° C.
  • a film of FePt fine particles 242 having a diameter of about 4 nm was formed on a glass substrate 240 by a solution reaction. Due to the solution reaction, the periphery of the FePt fine particle was covered with impurities such as carbon. Usually, most impurities are evaporated and disappear by a heat treatment of 500° C. or more, but this is not sufficient for using the FePt fine particle as the catalyst for the growth of carbon nanotubes. Therefore, after placing the substrate in a reaction part, hydrogen was introduced to adjust the pressure to 1 kPa and the substrate was annealed at 500° C., thereby completely cleaning the FePt fine particles.
  • the present invention provides a structure where a carbon nanotube is connected by a good ohmic contact to a metal material (for example, electrode material or wiring material) which is the objective of connection.
  • a metal material for example, electrode material or wiring material
  • This ohmic connection structure is formed simultaneously with the growth of carbon nanotube and therefore, this can dispense with a step of forming an ohmic connection structure, which has been conventionally performed in the lower junction part of via of an electronic device after the growth of nanotubes. Accordingly, in the case of applying the carbon nanotube as a longitudinal wiring via material, particularly for ULSI wiring, a good ohmic connection, which has been heretofore difficult to produce, can be formed between the nanotube and the lower junction part.
  • carbon nanotubes orientation-grown at a low temperature on a substrate can be obtained without relying on auxiliary means which has been heretofore used, such as electric field or plasma.

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Abstract

An electronic device having a structure of an ohmic connection to a carbon element cylindrical structure body, wherein a metal material is positioned inside the junction part of a carbon element cylindrical structure body joined to a connection objective and the carbon element cylindrical structure body and the connection objective are connected by an ohmic contact. Methods for producing such an electronic device are also disclosed. Further, a method for growing a carbon nanotube is disclosed.

Description

    CROSS-REFERENCES TO RELATED APPLICATIONS
  • This application is based upon and claims the benefit of priority from each of prior Japanese Patent Applications No. 2003-078353, filed on Mar. 20, 2003, and No. 2003-083192, filed on Mar. 25, 2003, the entire contents thereof being incorporated herein by reference. [0001]
  • BACKGROUND OF THE INVENTION
  • 1. Field of the Invention [0002]
  • The present invention relates to an electronic device having a structure for ohmic connection to a carbon element cylindrical structure body represented by a carbon nanotube and a production method thereof, which techniques are widely applicable when a carbon element cylindrical structure body is applied to an electronic device. [0003]
  • The present invention also relates to a method for growing carbon nanotubes. [0004]
  • 2. Description of the Related Art [0005]
  • In recent years, studies are being made on the use of a carbon element cylindrical structure body as an electrically conducting or semiconductor material in an electronic device. In the electronic device, a carbon element cylindrical structure body must be ohmically connected to an electrode or a wire so as to avoid an increase in electric resistance in the connection part. [0006]
  • FIG. 1 schematically shows the connection of a carbon element [0007] cylindrical structure body 11, which is formed as a longitudinal via material in a via hole of an electronic device, to a lower wiring Cu layer 13 and an upper wiring Cu layer 15. In a via hole formed in an interlayer insulating film 17 on the lower wiring layer 13, a bundle of carbon element cylindrical structure bodies 11 is formed in vertical orientation. The carbon element cylindrical structure body 11 is grown by using a chemical vapor deposition (CVD) method and, at this time, a catalyst metal (for example, Ni) layer 19, necessary for the growth of the carbon element cylindrical structure body, is present on the wiring layer exposed in the via hole. On the other hand, between the carbon element cylindrical structure body 11 and the upper wiring layer 15, a Ti layer 21 is inserted.
  • The connection between the carbon element [0008] cylindrical structure body 11 and the upper wiring layer 15 is an ohmic connection resulting from carbidization (formation into TiC) of the Ti layer 21 intervening therebetween. This method is a technique of contacting the carbon element cylindrical structure body with the Ti layer and then performing a heat treatment at a high temperature to cause TiC formation at the interface, thereby obtaining an ohmic connection (see, Y. Zhang et al., Science 285, 1719 (1999)).
  • As shown in FIG. 1, in the conventional structure, only a catalyst metal (Ni) [0009] layer 19, necessary for the growth of the carbon element cylindrical structure body 11, is present on the lower wiring (Cu) layer 13.
  • With respect to the production method of a carbon nanotube, arc discharge, laser evaporation, thermal CVD, plasma enhanced CVD and the like are known. By the arc discharge or laser evaporation method, a carbon nanotube having good quality can be obtained but the orientation or length of carbon nanotubes can hardly be controlled. [0010]
  • The method of enabling the control of the orientation or direction includes a thermal CVD method and a plasma enhanced CVD method. In these methods, carbon nanotubes can be orientation-grown by applying an electric field during the growth. The orientation growth in the case of not applying an electric field is described in [0011] Nature, Vol. 416, pp. 495-496 (2002), however, the growth temperature is as high as 800° C. or more and therefore, it is impossible to grow carbon nanotubes on a semiconductor circuit by this technique. Furthermore, the growth of carbon nanotubes at 550° C. is reported in Chemical Physics Letters, 360, pp. 2229-234 (2002), however, the growth direction cannot be controlled.
  • Various methods for producing carbon nanotubes by using thermal CVD are described in patent documents. For example, Japanese Unexamined Patent Publication (Kokai) No. 9-31757 (JP 9-31757 A) discloses a method of producing graphite nanotubes at a low temperature by CVD, where the graphite nanotube is produced at 650 to 800° C. Japanese Unexamined Patent Publication (Kokai) No. 10-203810 (JP 10-203810 A) describes a technique of growing carbon nanotubes on a substrate at a relatively low temperature, where the growth requires a plasma produced by a direct-current glow discharge. Japanese Unexamined Patent Publication (Kokai) No. 11-139815 (JP 11-139815 A) describes a method for producing a carbon nanotube device by using a thermal decomposition reaction of the starting material gas. Also, Japanese Unexamined Patent Publication (Kokai) No. 2001-303250 (JP 2001-303250 A) describes a method of vertically orienting carbon nanotubes on a substrate by using thermal CVD, where a direct current voltage is applied during the growth. [0012]
  • In these methods for producing carbon nanotubes by using thermal CVD, when auxiliary means such as an electric field is not used, a growth temperature of 500° C. or more is generally used. [0013]
  • A CVD method using a hot filament (hot-filament CVD) is also known. Japanese Unexamined Patent Publication (Kokai) No. 2000-353467 (JP 2000-353467 A) describes a method for producing a cold cathode device, where a diamond or diamond-like carbon electron-releasing material is formed by hot-filament CVD. The production of carbon nanotubes is not referred to therein. Japanese National Publication (Kohyo) No. 2002-518280 (JP 2002-518280 A) describes a method for growing carbon nanotubes by hot-filament CVD. In this method, an electric field is applied during the growth. [0014]
  • In this way, in conventional production of carbon nanotubes by hot-filament CVD, application of an electric field is performed as auxiliary means. [0015]
  • Also, a technique of growing carbon nanotubes at a filament temperature of 1,600° C. by hot-filament CVD is described in [0016] Chemical Physics Letters, 342, pp. 259-264 (2001).
  • SUMMARY OF THE INVENTION
  • The electronic device having a structure of an ohmic connection to a carbon element cylindrical structure body according to the present invention is characterized in that a metal material is positioned inside the junction part of a carbon element cylindrical structure body joined to a connection objective and the carbon element cylindrical structure body and the connection objective are connected by an ohmic contact. By virtue of connection through an ohmic contact, the increase in resistance at the connected part between the carbon element cylindrical structure body and the connection objective can be suppressed. [0017]
  • The electronic device having a structure of an ohmic connection to a carbon element cylindrical structure body of the present invention can be produced by a method comprising disposing a metal material on a connection objective capable of ohmically contacting with a carbon element cylindrical structure body, and forming a carbon element cylindrical structure body according to chemical vapor deposition using the metal material as the catalyst while accomplishing an ohmic contact between the carbon element cylindrical structure body and the connection objective. By using for the connection objective a material capable of ohmically contacting with a carbon element cylindrical structure body, an ohmic connection structure therebetween can be realized simultaneously with the growth of the carbon element cylindrical structure body. [0018]
  • Alternatively, the electronic device having a structure of an ohmic connection to a carbon element cylindrical structure body of the present invention can be produced by a method comprising forming a first stack of a first material capable of ohmically contacting with a carbon element cylindrical structure body and a second material of catalyst metal disposed on the first material, heat-treating the first stack in vacuum or in a hydrogen atmosphere to form a second stack made of a lower layer composed of an alloy of the first material and the second material, an intermediate layer composed of the first material and an upper layer composed of a fine particle formed of the second material, and forming a carbon element cylindrical structure body by chemical vapor deposition using the fine particle of the second material on the surface of the second stack as the catalyst to incorporate the fine particle of the second material into the inside of the carbon element cylindrical structure body and at the same time, connect, by an ohmic contact, the side wall of the carbon element cylindrical structure body to the intermediate layer composed of the first material. The carbon element cylindrical structure body grows on the first material capable of an ohmic contact by the action of the fine particle catalyst, so that the carbon element cylindrical structure body can be connected by an ohmic contact to the intermediate layer composed of the first material simultaneously with the growth of the carbon element cylindrical structure body. [0019]
  • The term “carbon element cylindrical structure body” as used herein is a linear nanostructure constituted by carbon atoms and this is a generic term for a carbon nanotube, a cup-stacked type structure, a carbon fiber or the like. [0020]
  • The method for growing a carbon nanotube of the present invention is a method comprising disposing a substrate in a growth chamber, supplying a starting material gas to the chamber and orientation-growing a carbon nanotube on the substrate by CVD, the method being characterized in that neither an electric field nor a plasma is used for the growth of the carbon nanotube and that heat generated from a filament disposed in the growth chamber is utilized. [0021]
  • By using the hot filament, carbon nanotubes can be orientation-grown at a relatively low temperature, specifically, even at a substrate growth face temperature of less than 500° C.[0022]
  • BRIEF DESCRIPTION OF THE DRAWINGS
  • The above and other objects and advantages of the invention will be well understood and appreciated by a person with ordinary skill in the art, from consideration of the following detailed description made by referring to the attached drawings, wherein: [0023]
  • FIG. 1 is a schematic view for explaining a conventional technique of using a carbon element cylindrical structure body for the longitudinal via material of an electronic device; [0024]
  • FIG. 2A is a schematic view for explaining a first embodiment of the present invention, where a carbon element cylindrical structure body is applied to the longitudinal via of an electronic device; [0025]
  • FIG. 2B is an enlarged view of the portion denoted by B in FIG. 2A; [0026]
  • FIG. 3A is a view for explaining a laminate film used in the method for producing a structure of an ohmic connection of the present invention; [0027]
  • FIG. 3B is a view for explaining a NiTi alloy layer obtained from the Ni/Ti laminate film of FIG. 3A; [0028]
  • FIG. 4A is a schematic partial enlarged view for explaining the first stack used in a second embodiment of the present invention; [0029]
  • FIG. 4B is a schematic partial enlarged view for explaining the second stack used in the second embodiment of the present invention; [0030]
  • FIGS. 5A to [0031] 5C are schematic views showing the production process in Example 1;
  • FIGS. 6A and 6B are schematic views showing the production process in Example 2; [0032]
  • FIG. 7 is a schematic view for explaining the method for growing carbon nanotubes of the present invention; [0033]
  • FIGS. 8A and 8B are views for explaining the growth of carbon nanotubes in Example 3; [0034]
  • FIGS. 9A and 9B are views for explaining the growth of carbon nanotubes in Example 4; and [0035]
  • FIGS. 10A and 10B are views for explaining the growth of carbon nanotubes in Example 5.[0036]
  • DETAILED DESCRIPTION OF THE INVENTION
  • As described above, the term “carbon element cylindrical structure body” as used herein is a linear nanostructure constituted by carbon atoms and this is a generic term for a carbon nanotube, a cup-stacked type structure, a carbon fiber or the like. In the following, the present invention is described by referring to carbon nanotube which is one representative of these nanostructures. [0037]
  • In a conventional structure, such as that shown in FIG. 1, a Ti layer is not present between the carbon element [0038] cylindrical structure body 11 and the lower wiring layer 13 and therefore, an ohmic contact by the TiC formation cannot be formed. Furthermore, as for the contact with the lower wiring layer 13, an ohmic contact cannot be formed as in the case of the upper wiring layer 15 by depositing a Ti layer after the growth of the carbon element cylindrical structure body 11 and, subsequently, performing a high-temperature heat treatment. That is, in the conventional structure, an ohmic contact ensuring sufficiently low resistance cannot be formed between the lower wiring layer and the carbon element cylindrical structure body and, thus, the wiring/via part formed by the carbon element cylindrical structure body disadvantageously has high resistance.
  • One of objects of a first aspect of the present invention is to provide an electronic device having a structure of an ohmic connection to a carbon element cylindrical structure body, which can be realized simultaneously with the growth of the carbon element cylindrical structure body, and a production method thereof. [0039]
  • FIGS. 2A and 2B schematically show an embodiment in which the present invention is applied to an electronic device having a longitudinal via. Within a via hole formed in an [0040] interlayer insulating film 37 on a lower wiring (Cu) layer 33, a bundle of carbon nanotubes 31 is formed in vertical orientation. In the present invention, as shown in FIG. 3A, a laminate film obtained by previously forming, on the lower wiring layer 33 in the via hole, a Ti layer 45 for the TiC formation of the junction part of the carbon nanotube 31 to the lower wiring layer 33 and forming thereon a catalyst metal (for example, Ni) layer necessary for the growth of nanotubes is used. When this Ni/Ti laminate film is used, the Ni/Ti laminate film is subject to an elevation of the substrate temperature at the time of growing carbon nanotubes by chemical vapor deposition and changes into a NiTi alloy layer 45 a (FIG. 3B). The carbon nanotube 31 grows on the surface of the NiTi alloy layer 45 a by using, as a nucleus, the catalyst metal Ni fine particle in the alloy. As shown in FIG. 2B, which is an enlarged view of the portion denoted by B in FIG. 2A, the Ni fine particle 39 is embraced in the inside at the root of the growing carbon nanotube 31 and the side wall of the nanotube 31 comes into contact with Ti remaining on the surface of the alloy layer 45 a. This contact portion 47 becomes the ohmic contact site where Ti is carbidized. In other words, an ohmic contact can be formed between the alloy layer 45 a and the nanotube 31 simultaneously with the growth of carbon nanotube.
  • In fact, when the contact resistance between the [0041] nanotube 11 or 31 and the lower wiring layer 13 or 33 was measured for the structures of conventional example (FIG. 1) and the present invention (FIG. 2), the resistance of the present invention was lower by single or double figures (conventional example: 15 MΩ, present invention: 130 kΩ). This result infers that when the present invention is used, TiC formation occurs at the contact portion between the carbon nanotube and the lower wiring layer simultaneously with the growth of carbon nanotube.
  • The [0042] carbon nanotube 31 formed within the via hole and the upper wiring layer 35 can be ohmically connected, as in the conventional art, by the carbidization (TiC formation) of the Ti layer 41 intervening therebetween. In this way, according to the present invention, the carbon nanotube can be connected by a good ohmic contact with both the lower and upper wiring layers 33 and 35 and a via with low resistance can be realized.
  • In the case described above (first embodiment), the connection objective to which the [0043] carbon nanotube 31 is ohmically connected is an alloy layer 45 a and the metal material thereon is a catalyst metal fine particle 39.
  • A second embodiment where the present invention is applied to an electronic device having a longitudinal via is described below. Similarly to the first embodiment described by referring to FIGS. 2A and 2B, as shown in FIG. 4A, a [0044] first stack 54 made of a Ti layer 52 for the TiC formation of the junction part of the carbon nanotube to the lower wiring layer 33 and a catalyst metal Ni layer 53 provided thereon is formed on the lower wiring layer 33 within a via hole. This stack is heat-treated in a vacuum or in a hydrogen atmosphere to form a second stack 61 constituted by, as shown in FIG. 4B which is a partial enlarged view similarly to FIG. 2B, a lower layer 55 of TiNi alloy, an intermediate layer 57 of Ti and an upper layer of Ni fine particle 59. Subsequently, chemical vapor deposition is performed by using the Ni fine particle on the surface of the stack 61 as the catalyst, whereby the Ni fine particle is incorporated inside the carbon nanotube 51 and, at the same time, a part of Ti in the intermediate layer 57 contacting with the bottom of the side wall of carbon nanotube 51 is carbidized to join the carbon nanotube 51 and the Ti intermediate layer 57 by ohmic contact.
  • In this embodiment, the [0045] Ti layer 57 corresponds to the connection objective to which the carbon nanotube is ohmically connected in the first embodiment, and the Ni fine particle 59 similarly corresponds to the metal material as the catalyst fine particle in the previous case.
  • The connection objective to which the carbon element cylindrical structure body is connected by an ohmic contact is the [0046] NiTi alloy layer 45 a in the first embodiment and this layer is derived from the Ti layer 45 which is previously formed. In the second embodiment, the connection objective is the Ti intermediate layer 57 and this layer is also derived from the Ti layer which is previously formed (Ti layer before heat treatment). In this meaning, in either embodiment, the connection objective to which the carbon nanotube is connected can be regarded as a Ti layer for carbidization (Ti layer before the heat treatment accompanying the growth of nanotubes (in the first embodiment) or Ti layer formed by the heat treatment before the growth of nanotube (in the second embodiment)), that is, a material of undergoing ohmic connection to the carbon nanotube by carbidization.
  • In the present invention, Nb, Si or C other than Ti can be used as the material (connection objective) undergoing an ohmic connection to carbon nanotube by carbidization. When the material as the connection objective is C (carbon), the carbon nanotube and the connection objective are connected by a carbon-carbon bond and, in the present invention, this connection by a carbon-carbon bond is also called herein connection by carbidization. [0047]
  • As the metal material acting as the catalyst for the growth of carbon nanotubes by CVD, Fe or Co can be used other than Ni. An alloy containing at least one metal selected from Ni, Fe and Co can also be used. [0048]
  • One of objects of a second aspect of the present invention is to provide a novel method capable of producing carbon nanotubes orientation-grown at a low temperature without relying on auxiliary means such as electric field (or plasma) which has been heretofore employed and, thereby, to enable the growth of carbon nanotubes on, for example, a semiconductor circuit which cannot be subjected to a high-temperature treatment. [0049]
  • In the method for growing carbon nanotubes of the present invention, a filament disposed in the growth chamber is used as a heat source for the growth of carbon nanotubes by CVD. Such a CVD process using a filament for heating (called a hot filament) is known as hot-filament CVD but in conventional techniques of using this method for the growth of carbon nanotubes, a filament temperature of 1,600° C. is required (see, [0050] Chemical Physics Letters, 342, pp. 259-264 (2001)).
  • The hot filament generates a heat upon passing of a current. The filament temperature at the growth of carbon nanotubes is preferably 400° C. or more. If the filament temperature is less than 400° C., this is insufficient to supply an energy for decomposing the starting material gas, whereas if it is unnecessarily elevated, the energy is wasted. Therefore, the filament temperature in general is preferably from 400 to 1,000° C., more preferably from 400 to 600° C., still more preferably from 400 to 500° C. [0051]
  • The hot-filament should be produced from a material capable of enduring high temperature (400° C. or more) at the growth of carbon nanotubes and at the same time, undergoing no or little chemical reaction with the starting material gas or a decomposition product thereof. The present inventors have found that for the purpose of producing carbon nanotubes by CVD from a starting material gas containing a carbon source, a filament made of rhenium or a material mainly comprising rhenium is suitable. [0052]
  • As shown in FIG. 7, a hot-[0053] filament 212 is disposed to face a growth substrate 214 in a vacuum chamber (reaction chamber) 210 to which a starting material gas is supplied. The distance between the filament 212 and the substrate 214 is determined according to the carbon nanotube growth conditions (e.g., the kind of starting material gas used and the growth rate).
  • At the growth, the [0054] hot filament 212 can be moved above the substrate 214 to uniformly grow carbon nanotubes in an arbitrary area. Also, the substrate 214 may be moved by fixing the position of the hot filament 212. Alternatively, the hot filament 212 and the substrate 214 both may be relatively moved. As for the mode of movement, for example, rotation or reciprocation can be employed. For example, in FIG. 7, the filament 212 can be made to cause a reciprocating movement in the horizontal direction while moving the substrate 214 in the vertical direction by the movement of a substrate stage 216. The filament 212 is connected to, for example, an A.C. power source 218 and the substrate stage 216 is generally equipped with substrate heating means (not shown).
  • A carbon source gas containing carbon is used as the starting material for the growth of carbon nanotubes. The carbon source gas may be a hydrocarbon gas such as methane, ethane, acetylene, propane or butane, or a gas of alcohols such as methanol or ethanol. A mixture of two or more carbon sources may also be used. [0055]
  • The starting material gas may contain, in addition to the carbon source, one or both of a reactive gas such as hydrogen and an inert gas such as helium or argon. [0056]
  • The total pressure of the starting material gas in the growth chamber may be approximately from 0.1 to 100 kPa. If the pressure is less than 0.1 kPa, the growth rate of carbon nanotubes decreases, whereas if it exceeds 100 kPa, there may be a danger of the starting material gas leaking out of the growth chamber. The total pressure of the starting material gas is preferably from 0.1 to 10 kPa, more preferably from 0.3 to 10 kPa. [0057]
  • A substance acting as the catalyst for the growth reaction must be present on the substrate surface where carbon nanotubes are grown. As the catalyst, a transition metal such as Fe, Ni, Co or Pd may be used and an alloy of two or more of these transition metals may also be used. Furthermore, an alloy of such a transition metal capable of acting as the catalyst and a metal of not acting as the catalyst, for example, Fe—Pt and Co—Pt, may also be used. [0058]
  • The catalyst may form a thin film on the surface of the growth substrate or may be a fine particle dispersed on the substrate surface. In the case of a fine particle catalyst, the diameter of the growing carbon nanotube can be controlled by controlling the diameter of the fine particle. For example, as described in Examples later, when fine particle catalysts having diameters of about 7 nm and 4 nm were used, carbon nanotubes having diameters of about 15 nm and 8 nm could be obtained, respectively. [0059]
  • The thin-film catalyst may be formed by any method. For example, evaporation or sputtering can be used. The thickness of the thin film can be arbitrarily selected. On the other hand, the fine particle catalyst can be formed by utilizing laser ablation or a solution reaction. In the case of using a solution reaction, impurities such as carbon are sometimes attached to the periphery of the fine particle formed. The impurities are generally evaporated and disappear by heat treatment at a high temperature of 500° C. or more, however, in some cases, the impurities cannot be completely removed by this heat treatment only. In such a case, the remaining impurities can be removed by, for example, an annealing treatment using a reactive gas such as hydrogen. The annealing can be performed under conditions the same as or close to the temperature and pressure conditions at the growth. Therefore, this treatment can be performed in the growth chamber before the growth of carbon nanotubes is started, and, subsequently, the growth of carbon nanotubes can be performed in the same growth chamber. [0060]
  • In the present invention, a hot-filament is used, whereby the carbon nanotube can be orientation-grown at a relatively low temperature. According to the method of the present invention, a temperature of 600° C. or less of the growth surface of the substrate is sufficient for obtaining carbon nanotubes. The temperature of the growth surface of the substrate may even be less than 500° C. [0061]
  • As for the substrate on which carbon nanotubes are grown, for example, a substrate of a semiconductor represented by silicon can be used. As described above, the temperature of the substrate surface can be relatively low and therefore, a substrate material which cannot be used as the substrate for the growth of carbon nanotubes in conventional CVD methods, such as a glass substrate, can also be used. [0062]
  • In producing carbon nanotubes by the present invention, an apparatus where a growth substrate is contained and a starting material gas is supplied to orientation-grow carbon nanotubes on the substrate by CVD and where a hot filament is equipped in the growth chamber, is used. [0063]
  • EXAMPLES
  • The present invention is described in greater detail below by referring to Examples, however, the present invention is not limited thereto. [0064]
  • Example 1
  • In this Example, a case where the present invention is applied to an electronic device having a wiring via is described. [0065]
  • As shown in FIG. 5A, an SiO[0066] 2 interlayer insulating film 103 (500 nm) is deposited on a lower wiring Cu layer 101 on a substrate (not shown) and thereon, a resist pattern (not shown) having openings, in the regions at which wiring vias are to be formed, is formed. By using the resist pattern as the mask, a wiring via 105 is formed in the interlayer insulating film 103. Thereafter, a Ti layer (50 nm) and an Ni catalyst metal layer (10 nm) are deposited in this order on the entire surface of the substrate by sputtering or evaporation. Subsequently, a Ti layer 107 (50 nm)/Ni layer 109 (10 nm) laminate film is caused to remain in the wiring via by the lift-off method using the resist film. In place of the Ni layer, a layer formed of Fe or Co may be used as the catalyst metal layer or a layer of an alloy containing at least one of Ni, Fe and Co may also be used. Also, in place of the thin layer of catalyst metal, a fine particle may be used. Furthermore, in place of the Ti layer, an Nb layer, an Si layer or a graphite carbon layer may be used.
  • In the wiring via [0067] 105, carbon nanotubes 111 are grown by CVD (see, FIG. 5B). For the growth of carbon nanotubes, for example, thermal CVD is used. In this case, the substrate is placed in a vacuum chamber (reaction chamber) and, for example, a mixed gas of acetylene and hydrogen at flow rates of 80 sccm and 20 sccm, respectively, is introduced as a reaction gas into the vacuum chamber and the pressure and substrate temperature are set to 200 Pa and 900° C., respectively. Also, hot-filament CVD, for performing gas dissociation by a hot filament, may be used. In this case, for example, a mixed gas of acetylene and hydrogen at flow rates of 80 sccm and 20 sccm, respectively, is introduced as a reaction gas into the vacuum chamber and the pressure, substrate temperature and hot filament temperature are set to 1,000 Pa, 600° C. and 1,800° C., respectively. Alternatively, DC plasma enhanced hot-filament CVD, combining direct-current (DC) plasma and a hot filament, may also be used. In this case, for example, a mixed gas of acetylene and hydrogen, at flow rates of 80 sccm and 20 sccm, respectively, is introduced as a reaction gas into the vacuum chamber and the pressure, substrate temperature and hot filament temperature are set to 1,000 Pa, 600° C. and 1,800° C., respectively. In order to vertically orient the carbon nanotubes, a direct-current (DC) electric field of −400 V was applied to the substrate with respect to the chamber (grounded). The application of direct-current (DC) electric field is advantageous for obtaining perpendicularly oriented carbon nanotubes with respect to the substrate. The carbon nanotubes 111 are grown by taking the Ni fine particle 109 a into the inside at the root from the Ni layer 109 and ohmically connected to the Ti layer 107 through TiC generated by the partial carbidization of Ti in the lower layer 107.
  • Before the growth of carbon nanotubes, the substrate in the vacuum chamber may be heat-treated (for example, at 600° C. for 30 minutes) in vacuum or in a hydrogen atmosphere to alloy the Ni/Ti laminate film. By this heat treatment, an Ni fine particle, a Ti layer and an NiTi alloy layer are formed in this order from the film surface. Thereafter, the [0068] carbon nanotube 111 is grown by CVD while incorporating the Ni fine particle in the uppermost part as the catalyst metal into the inside of the tube side wall and at the same time, the side wall of the nanotube is joined with the Ti layer 107 a lying beneath.
  • Then, as shown in FIG. 5C, a Ti layer [0069] 113 (50 nm) and a Cu layer 115 (500 nm) are deposited in this order by sputtering or evaporation. Subsequently, a heat treatment (for example, 500 to 800° C. for 30 minutes) is performed to cause TiC formation in the upper end of the carbon nanotube 111. As a result, the carbon nanotube 111 was connected by ohmic contact to the upper and lower wiring layers 101 and 115.
  • Example 2
  • In this Example, a case where the present invention is applied to an electronic device having a transverse wiring is described. [0070]
  • As shown in FIG. 6A, an SiO[0071] 2 insulating film 123 (500 nm) is deposited on an Si substrate 121 and thereon, a resist pattern (not shown) having openings in the regions, at which electrodes are to be formed, is formed. On the entire surface of the substrate, a Ti layer (50 nm) and an Ni catalyst metal layer (10 nm) are deposited in this order by sputtering or evaporation. Subsequently, only a Ti layer 125 (50 nm)/Ni layer 127 (10 nm) laminate film (electrode pattern) in the openings of the resist pattern is caused to remain by the lift-off method using the resist film.
  • Between a pair of opposing electrode patterns, a [0072] carbon nanotube 129 is grown by CVD (see, FIG. 6B). The CVD and growth conditions used may be the same as those described in Example 1. Also, similarly to Example 1, the Ni/Ti laminate film may be heat-treated in advance of the growth of carbon nanotube by CVD. In order to transversely orient the carbon nanotube in parallel to the substrate surface, a direct-current (DC) electric field of 400 V was applied between electrodes. The carbon nanotube 129 is grown by incorporating a part of Ni in the Ni layer 127 as a catalyst element 127 a into the inside and is ohmically connected to the Ti layer 125 through TiC generated by partial carbidization of Ti in the Ti layer 125.
  • Example 3
  • As shown in FIG. 8A, an Ni [0073] thin film 222 for catalyst was formed on a silicon substrate 220 by evaporation and, thereon, an SiN insulating film 224 (thickness: 500 nm) having an opening with a diameter of 2 μm was formed. The thickness of the Ni thin film 222 can be arbitrarily decided, but the thickness was set here to 2 nm. This substrate was introduced into a reaction part (vacuum chamber) (not shown) and the substrate temperature was set to 500° C. A starting material gas prepared by mixing argon and acetylene at a ratio of 80:20 was supplied to the reaction part at a flow rate of 100 ccm and the total gas pressure in the reaction part was adjusted to 1 kPa by the control in an exhaust system connected to a vacuum pump. A hot filament (made of rhenium) was moved above the substrate and with a distance of about 6 mm to the substrate, a current of about 8 A was passed. By this passing of a current, the hot filament temperature was elevated to 800° C. After maintaining this state for 1 minute, the passing of the current to the hot filament was stopped. The remaining starting material gas in the reaction part was vacuum-evacuated and the substrate was taken out from the reaction part. As shown in FIG. 8B, carbon nanotubes 226 having a length of about 2 μm were formed in the vertical direction from the substrate surface.
  • Example 4
  • As shown in FIG. 9A, a film of Fe [0074] fine particles 232 having a diameter of 7 nm was formed by laser ablation in an opening with a diameter of 2 μm of an SiN insulating film 234 (thickness: 500 nm) formed on a silicon substrate 230. This substrate was introduced into a reaction part and the substrate temperature was set to 400° C. A starting material gas, prepared by mixing argon, acetylene and hydrogen at a ratio of 24:6:70, was supplied to the reaction part and the total pressure in the reaction part was adjusted to 1.3 kPa. A current of about 0.7 A was passed to a hot filament moved above the substrate and the hot filament temperature was set to about 400° C. After maintaining this state for 15 minutes, the passing of a current was stopped. The remaining starting material gas in the reaction part was vacuum-exhausted and the substrate was taken out from the reaction part. As shown in FIG. 9B, carbon nanotubes 236 having a length of about 2 μm and a diameter of about 15 nm were formed in the vertical direction from the substrate surface.
  • Example 5
  • As shown in FIG. 10A, a film of FePt [0075] fine particles 242 having a diameter of about 4 nm was formed on a glass substrate 240 by a solution reaction. Due to the solution reaction, the periphery of the FePt fine particle was covered with impurities such as carbon. Usually, most impurities are evaporated and disappear by a heat treatment of 500° C. or more, but this is not sufficient for using the FePt fine particle as the catalyst for the growth of carbon nanotubes. Therefore, after placing the substrate in a reaction part, hydrogen was introduced to adjust the pressure to 1 kPa and the substrate was annealed at 500° C., thereby completely cleaning the FePt fine particles.
  • Thereafter, a 95:1:4 mixed gas of hydrogen, acetylene and argon was supplied to the reaction part and the total pressure in the reaction part was set to 1 kPa. A current of 10 A was passed through a hot filament moving above the substrate heated to 500° C. and this state was maintained for 10 minutes. As shown in FIG. 10B, [0076] carbon nanotubes 244 having a length of about 2 μm and a diameter of about 8 nm were formed in the vertical direction from the substrate surface.
  • As described, the present invention provides a structure where a carbon nanotube is connected by a good ohmic contact to a metal material (for example, electrode material or wiring material) which is the objective of connection. This ohmic connection structure is formed simultaneously with the growth of carbon nanotube and therefore, this can dispense with a step of forming an ohmic connection structure, which has been conventionally performed in the lower junction part of via of an electronic device after the growth of nanotubes. Accordingly, in the case of applying the carbon nanotube as a longitudinal wiring via material, particularly for ULSI wiring, a good ohmic connection, which has been heretofore difficult to produce, can be formed between the nanotube and the lower junction part. [0077]
  • Furthermore, according to the present invention, carbon nanotubes orientation-grown at a low temperature on a substrate can be obtained without relying on auxiliary means which has been heretofore used, such as electric field or plasma. [0078]

Claims (36)

1. An electronic device having a structure of an ohmic connection to a carbon element cylindrical structure body, wherein a metal material is positioned inside the junction part of a carbon element cylindrical structure body joined to a connection objective and the carbon element cylindrical structure body and the connection objective are connected by an ohmic contact.
2. The electronic device as claimed in claim 1, wherein said metal material is Ni, Fe or Co, or an alloy containing at least one of Ni, Fe and Co.
3. The electronic device as claimed in claim 1, wherein the material of said connection objective is Ti, Nb, Si or C.
4. The electronic device as claimed in claim 1, wherein said connection objective is a part of the wiring in an electronic device.
5. The electronic device as claimed in claim 1, wherein said carbon element cylindrical structure body is a carbon nanotube.
6. A method for producing an electronic device having a structure of ohmic connection to a carbon element cylindrical structure body, comprising disposing a metal material on a connection objective capable of ohmically contacting a carbon element cylindrical structure body and forming a carbon element cylindrical structure body by chemical vapor deposition using said metal material as the catalyst while accomplishing an ohmic contact between the carbon element cylindrical structure body and the connection objective.
7. The method for producing an electronic device as claimed in claim 6, wherein the material of said connection objective is alloyed with said metal material by the elevation of temperature during said chemical vapor deposition and a carbon element cylindrical structure body is grown using the particle of said metal material in said alloy as the catalyst for said chemical vapor deposition.
8. The method for producing an electronic device as claimed in claim 6, wherein the material of said connection objective is Ti, Nb, Si or C.
9. The method for producing an electronic device as claimed in claim 6, wherein said metal material is Ni, Fe or Co, or an alloy containing at least one of Ni, Fe and Co.
10. The method for producing an electronic device as claimed in claim 6, wherein said chemical vapor deposition is performed by applying an electric field in the growth direction of the carbon element cylindrical structure body.
11. The method for producing an electronic device as claimed in claim 6, wherein said carbon element cylindrical structure body is a carbon nanotube.
12. A method for producing an electronic device having a structure of ohmic connection to a carbon element cylindrical structure body, comprising forming a first stack of a first material capable of ohmically contacting a carbon element cylindrical structure body and a second material of catalyst metal disposed on said first material, heat-treating said first stack in vacuum or in a hydrogen atmosphere to form a second stack made of a lower layer composed of an alloy of the first material and the second material, an intermediate layer composed of the first material and an upper layer composed of a fine particle of the second material, and forming a carbon element cylindrical structure body by chemical vapor deposition using the fine particle of the second material on the surface of said second stack as the catalyst to incorporate the fine particle of the second material into the inside of the carbon element cylindrical structure body and at the same time, connect, by ohmic contact, the side wall of the carbon element cylindrical structure body to the intermediate layer composed of the first material.
13. The method for producing an electronic device as claimed in claim 12, wherein said first material is Ti, Nb, Si or C.
14. The method for producing an electronic device as claimed in claim 12, wherein said second material is Ni, Fe or Co, or an alloy containing at least one of Ni, Fe and Co.
15. The method for producing an electronic device as claimed in claim 12, wherein said chemical vapor deposition is performed by applying an electric field in the growth direction of the carbon element cylindrical structure body.
16. The method for producing an electronic device as claimed in claim 12, wherein said carbon element cylindrical body is a carbon nanotube.
17. A method for growing a carbon nanotube, comprising disposing a substrate in a growth chamber, supplying a starting material gas to the chamber, and orientation-growing a carbon nanotube on the substrate by CVD, wherein the growth of the carbon nanotube uses neither an electric field nor a plasma but uses heat generated from a filament disposed in the growth chamber.
18. The method for growing a carbon nanotube as claimed in claim 17, wherein the temperature of said filament during the growth of the carbon nanotube is 400° C. or more.
19. The method for growing a carbon nanotube as claimed in claim 17, wherein said filament is a filament made of rhenium or a material mainly comprising rhenium.
20. The method for growing a carbon nanotube as claimed in claim 17, wherein said starting material gas is a gas of a carbon source.
21. The method for growing a carbon nanotube as claimed in claim 20, wherein said carbon source is a hydrocarbon, an alcohol or a mixture thereof.
22. The method for growing a carbon nanotube as claimed in claim 21, wherein said hydrocarbon is methane, ethane, acetylene, propane, butane or a mixture of two or more thereof.
23. The method for growing a carbon nanotube as claimed in claim 21, wherein said alcohol is methanol, ethanol or a mixture thereof.
24. The method for growing a carbon nanotube as claimed in claim 20, wherein said starting material gas further contains one or both of a reactive gas and an inert gas.
25. The method for growing a carbon nanotube as claimed in claim 24, wherein said reactive gas is hydrogen.
26. The method for growing a carbon nanotube as claimed in claim 24, wherein said inert gas is helium or argon.
27. The method for growing a carbon nanotube as claimed in claim 17, wherein the total pressure of said starting material gas in the growth chamber is 0.1 to 100 kPa.
28. The method for growing a carbon nanotube as claimed in claim 17, wherein a thin film-like or fine particle-like carbon nanotube growth catalyst formed on the substrate surface is used.
29. The method for growing a carbon nanotube as claimed in claim 28, wherein said fine particle-like catalyst is used as said catalyst and the diameter of the growing carbon nanotube is controlled by the diameter of said fine particle-like catalyst.
30. The method for growing a carbon nanotube as claimed in claim 29, wherein said fine particle-like catalyst formed on said substrate is annealed in the growth chamber and in the presence of a reactive gas to remove impurities from the fine particle-like catalyst before the growth of the carbon nanotube.
31. The method for growing a carbon nanotube as claimed in claim 28, wherein said catalyst is a transition metal Fe, Ni, Co or Pd capable of acting as the catalyst for the growth of the carbon nanotube, or an alloy of two or more thereof.
32. The method for growing a carbon nanotube as claimed in claim 28, wherein said catalyst is an alloy of a transition metal capable of acting as the catalyst for the growth of the carbon nanotube and a metal which does not act as the catalyst.
33. The method for growing a carbon nanotube as claimed in claim 32, wherein said alloy is an Fe—Pt or Co—Pt alloy.
34. The method for growing a carbon nanotube as claimed in claim 17, wherein during the growth of carbon nanotubes, one or both of said filament and said substrate are moved relatively.
35. The method for growing a carbon nanotube as claimed in claim 17, wherein said substrate is a semiconductor or glass substrate.
36. The method for growing a carbon nanotube as claimed in claim 17, wherein the growth face temperature of said substrate during the growth of the carbon nanotube is 600° C. or less.
US10/773,311 2003-03-20 2004-02-09 Method for growing carbon nanotubes, and electronic device having structure of ohmic connection to carbon element cylindrical structure body and production method thereof Abandoned US20040182600A1 (en)

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Cited By (33)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20050046017A1 (en) * 2003-08-25 2005-03-03 Carlos Dangelo System and method using self-assembled nano structures in the design and fabrication of an integrated circuit micro-cooler
US20050224220A1 (en) * 2003-03-11 2005-10-13 Jun Li Nanoengineered thermal materials based on carbon nanotube array composites
US20050287689A1 (en) * 2004-06-23 2005-12-29 Canon Kabushiki Kaisha Method for manufacturing carbon fibers, method for manufacturing electron-emitting device using the same, method for manufacturing electronic device, method for manufacturing image display device, and information display reproduction apparatus using the same
US20050285116A1 (en) * 2004-06-29 2005-12-29 Yongqian Wang Electronic assembly with carbon nanotube contact formations or interconnections
US20060238990A1 (en) * 2005-03-21 2006-10-26 Ephraim Suhir Apparatus for attaching a cooling structure to an integrated circuit
US20060278901A1 (en) * 2003-01-24 2006-12-14 Carlos Dangelo In-chip structures and methods for removing heat from integrated circuits
US20060292716A1 (en) * 2005-06-27 2006-12-28 Lsi Logic Corporation Use selective growth metallization to improve electrical connection between carbon nanotubes and electrodes
US20070096304A1 (en) * 2005-08-26 2007-05-03 Kabir Mohammad S Interconnects and heat dissipators based on nanostructures
US20070205450A1 (en) * 2004-10-22 2007-09-06 Fujitsu Limited Semiconductor device and method of manufacturing the same
US20080096293A1 (en) * 2006-10-24 2008-04-24 Ephraim Suhir Method and Apparatus for Evaluation and Improvement of Mechanical and Thermal Properties of CNT/CNF Arrays
US20080095937A1 (en) * 2006-05-18 2008-04-24 California Institute Of Technology Robust filament assembly for a hot-wire chemical vapor deposition system
US20080128116A1 (en) * 2003-08-25 2008-06-05 Carlos Dangelo Vapor chamber heat sink having a carbon nanotube fluid interface
DE102008004183A1 (en) 2007-01-12 2008-07-31 Samsung Electronics Co., Ltd., Suwon Integrated circuit device has several carbon nanotubes that are formed in opening of insulation layer so that nanotubes are electrically connected to copper pattern through catalyst metal layer and barrier layer
US20080246148A1 (en) * 2007-01-12 2008-10-09 Samsung Electronics Co., Ltd. Electrical Interconnect Structures Having Carbon Nanotubes Therein and Methods of Forming Same
US20080246149A1 (en) * 2007-04-06 2008-10-09 Hynix Semiconductor Inc. Semiconductor device and method for forming device isolation film of semiconductor device
FR2917894A1 (en) * 2007-06-22 2008-12-26 Commissariat Energie Atomique Catalyst locating method for microelectronic industry, involves filling opening with filling material after depositing catalyst on upper surface of layer, removing catalyst deposited on surface, and removing filling material
US20090072408A1 (en) * 2007-09-12 2009-03-19 Smoltek Ab Connecting and Bonding Adjacent Layers with Nanostructures
US20090108251A1 (en) * 2005-04-25 2009-04-30 Mohammad Shafiqul Kabir Controlled growth of a nanostructure on a substrate
US7538422B2 (en) 2003-08-25 2009-05-26 Nanoconduction Inc. Integrated circuit micro-cooler having multi-layers of tubes of a CNT array
US20090159985A1 (en) * 2007-12-21 2009-06-25 Advanced Micro Devices, Inc. Integrated circuit system with contact integration
US20090233124A1 (en) * 2008-02-25 2009-09-17 Smoltek Ab Deposition and Selective Removal of Conducting Helplayer for Nanostructure Processing
US7776682B1 (en) * 2005-04-20 2010-08-17 Spansion Llc Ordered porosity to direct memory element formation
US20100264544A1 (en) * 2006-01-20 2010-10-21 Jang-Eun Heo Device including contact structure and method of forming the same
US20100313951A1 (en) * 2009-06-10 2010-12-16 Applied Materials, Inc. Carbon nanotube-based solar cells
US20100327444A1 (en) * 2008-02-29 2010-12-30 Fujitsu Limited Sheet structure, semiconductor device and method of growing carbon structure
US7897529B2 (en) 2007-03-23 2011-03-01 Lydall, Inc. Substrate for carrying catalytic particles
WO2011023519A1 (en) * 2009-08-28 2011-03-03 International Business Machines Corporation Selective nanotube growth inside vias using an ion beam
US20110240349A1 (en) * 2008-09-22 2011-10-06 Lakshmi Supriya Multiple die structure and method of forming a connection between first and second dies in same
JP2012528937A (en) * 2009-06-02 2012-11-15 フラウンホッファー−ゲゼルシャフト ツァ フェルダールング デァ アンゲヴァンテン フォアシュンク エー.ファオ Coating apparatus and coating method
US20130206461A1 (en) * 2012-02-13 2013-08-15 Tyco Electronics Corporation Electrical Conductors and Methods of Manufacturing Electrical Conductors
US20140374897A1 (en) * 2013-06-19 2014-12-25 Broadcom Corporation Thermal interface material for integrated circuit package and method of making the same
CN105226006A (en) * 2014-06-12 2016-01-06 中芯国际集成电路制造(上海)有限公司 The formation method of interconnection structure
CN111470468A (en) * 2020-04-22 2020-07-31 华中科技大学 Method for transferring vertical carbon nano tube to target substrate

Families Citing this family (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8907384B2 (en) * 2006-01-26 2014-12-09 Nanoselect, Inc. CNT-based sensors: devices, processes and uses thereof
US20090278556A1 (en) * 2006-01-26 2009-11-12 Nanoselect, Inc. Carbon Nanostructure Electrode Based Sensors: Devices, Processes and Uses Thereof
KR101979955B1 (en) 2009-05-18 2019-05-17 젠썸 인코포레이티드 Battery thermal management system
US8722222B2 (en) 2011-07-11 2014-05-13 Gentherm Incorporated Thermoelectric-based thermal management of electrical devices
US8624396B2 (en) * 2012-06-14 2014-01-07 Taiwan Semiconductor Manufacturing Company, Ltd. Apparatus and method for low contact resistance carbon nanotube interconnect
CN108155430B (en) 2013-01-14 2021-10-29 詹思姆公司 Thermoelectric-based thermal management of electrical devices
WO2014120688A1 (en) 2013-01-30 2014-08-07 Gentherm Incorporated Thermoelectric-based thermal management system
DE112014004953T5 (en) 2013-10-29 2016-07-14 Gentherm Incorporated Battery thermal management with thermoelectrics
CN106717139B (en) 2014-09-12 2019-07-12 詹思姆公司 Graphite thermoelectricity and/or resistance heat management system and method
WO2020112902A1 (en) 2018-11-30 2020-06-04 Gentherm Incorporated Thermoelectric conditioning system and methods
US11152557B2 (en) 2019-02-20 2021-10-19 Gentherm Incorporated Thermoelectric module with integrated printed circuit board

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20020163079A1 (en) * 2001-05-02 2002-11-07 Fujitsu Limited Integrated circuit device and method of producing the same
US20020167375A1 (en) * 2001-03-30 2002-11-14 Hoppe Daniel J. Carbon nanotube array RF filter

Family Cites Families (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2973352B2 (en) 1995-07-10 1999-11-08 科学技術振興事業団 How to make graphite fiber
JPH10203810A (en) 1997-01-21 1998-08-04 Canon Inc Production of carbon nanotube
JPH11116218A (en) 1997-10-17 1999-04-27 Osaka Gas Co Ltd Production of single layered nanotube
JP3363759B2 (en) 1997-11-07 2003-01-08 キヤノン株式会社 Carbon nanotube device and method of manufacturing the same
WO1999065821A1 (en) 1998-06-19 1999-12-23 The Research Foundation Of State University Of New York Free-standing and aligned carbon nanotubes and synthesis thereof
US6232706B1 (en) 1998-11-12 2001-05-15 The Board Of Trustees Of The Leland Stanford Junior University Self-oriented bundles of carbon nanotubes and method of making same
JP2000353467A (en) 1999-04-09 2000-12-19 Nec Corp Manufacture of cold cathode device
KR100376197B1 (en) 1999-06-15 2003-03-15 일진나노텍 주식회사 Low temperature synthesis of carbon nanotubes using metal catalyst layer for decompsing carbon source gas
KR100360470B1 (en) 2000-03-15 2002-11-09 삼성에스디아이 주식회사 Method for depositing a vertically aligned carbon nanotubes using thermal chemical vapor deposition
JP2002110567A (en) 2000-10-03 2002-04-12 Mitsubishi Electric Corp Chemical vapor phase deposition apparatus and method of forming film on semiconductor wafer
JP2002179418A (en) 2000-12-13 2002-06-26 Tohoku Techno Arch Co Ltd Method for forming carbon nanotube
JP2002212729A (en) 2001-01-17 2002-07-31 Hitachi Kokusai Electric Inc Substrate processor and method for producing semiconductor device
JP2002293524A (en) 2001-03-30 2002-10-09 Osaka Gas Co Ltd Production method of vapor phase growth carbon nanotube and its apparatus
JP3554287B2 (en) 2001-04-26 2004-08-18 三菱電機株式会社 Chemical vapor deposition apparatus and chemical vapor deposition method
US6787122B2 (en) * 2001-06-18 2004-09-07 The University Of North Carolina At Chapel Hill Method of making nanotube-based material with enhanced electron field emission properties
JP2004238258A (en) 2003-02-06 2004-08-26 Ulvac Japan Ltd Manufacturing method of carbonaceous matter

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20020167375A1 (en) * 2001-03-30 2002-11-14 Hoppe Daniel J. Carbon nanotube array RF filter
US20020163079A1 (en) * 2001-05-02 2002-11-07 Fujitsu Limited Integrated circuit device and method of producing the same
US7084507B2 (en) * 2001-05-02 2006-08-01 Fujitsu Limited Integrated circuit device and method of producing the same

Cited By (81)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20060278901A1 (en) * 2003-01-24 2006-12-14 Carlos Dangelo In-chip structures and methods for removing heat from integrated circuits
US7656027B2 (en) 2003-01-24 2010-02-02 Nanoconduction, Inc. In-chip structures and methods for removing heat from integrated circuits
US20050224220A1 (en) * 2003-03-11 2005-10-13 Jun Li Nanoengineered thermal materials based on carbon nanotube array composites
US7273095B2 (en) 2003-03-11 2007-09-25 United States Of America As Represented By The Administrator Of The National Aeronautics And Space Administration Nanoengineered thermal materials based on carbon nanotube array composites
US20070163769A9 (en) * 2003-03-11 2007-07-19 Jun Li Nanoengineered thermal materials based on carbon nanotube array composites
US7538422B2 (en) 2003-08-25 2009-05-26 Nanoconduction Inc. Integrated circuit micro-cooler having multi-layers of tubes of a CNT array
US20050046017A1 (en) * 2003-08-25 2005-03-03 Carlos Dangelo System and method using self-assembled nano structures in the design and fabrication of an integrated circuit micro-cooler
US7732918B2 (en) 2003-08-25 2010-06-08 Nanoconduction, Inc. Vapor chamber heat sink having a carbon nanotube fluid interface
US8039953B2 (en) 2003-08-25 2011-10-18 Samsung Electronics Co., Ltd. System and method using self-assembled nano structures in the design and fabrication of an integrated circuit micro-cooler
US7109581B2 (en) 2003-08-25 2006-09-19 Nanoconduction, Inc. System and method using self-assembled nano structures in the design and fabrication of an integrated circuit micro-cooler
US20080128116A1 (en) * 2003-08-25 2008-06-05 Carlos Dangelo Vapor chamber heat sink having a carbon nanotube fluid interface
US20060270116A1 (en) * 2003-08-25 2006-11-30 Nanoconduction, Inc. System and method using self-assembled nano structures in the design and fabrication of an integrated circuit micro-cooler
US7784531B1 (en) 2004-04-13 2010-08-31 The United States Of America As Represented By The Administrator Of The National Aeronautics And Space Administration Nanoengineered thermal materials based on carbon nanotube array composites
US20050287689A1 (en) * 2004-06-23 2005-12-29 Canon Kabushiki Kaisha Method for manufacturing carbon fibers, method for manufacturing electron-emitting device using the same, method for manufacturing electronic device, method for manufacturing image display device, and information display reproduction apparatus using the same
US20050285116A1 (en) * 2004-06-29 2005-12-29 Yongqian Wang Electronic assembly with carbon nanotube contact formations or interconnections
US20070205450A1 (en) * 2004-10-22 2007-09-06 Fujitsu Limited Semiconductor device and method of manufacturing the same
US7700978B2 (en) * 2004-10-22 2010-04-20 Fujitsu Microelectronics Limited Semiconductor device and method of manufacturing the same
US8034676B2 (en) * 2004-10-22 2011-10-11 Fujitsu Semiconductor Limited Semiconductor device and method of manufacturing the same
US20100144104A1 (en) * 2004-10-22 2010-06-10 Fujitsu Microelectronics Limited Semiconductor device and method of manufacturing the same
US7477527B2 (en) 2005-03-21 2009-01-13 Nanoconduction, Inc. Apparatus for attaching a cooling structure to an integrated circuit
US20060238990A1 (en) * 2005-03-21 2006-10-26 Ephraim Suhir Apparatus for attaching a cooling structure to an integrated circuit
US7776682B1 (en) * 2005-04-20 2010-08-17 Spansion Llc Ordered porosity to direct memory element formation
US7687876B2 (en) 2005-04-25 2010-03-30 Smoltek Ab Controlled growth of a nanostructure on a substrate
US20100171093A1 (en) * 2005-04-25 2010-07-08 Smoltek Ab Controlled Growth of a Nanostructure on a Substrate, and Electron Emission Devices Based on the Same
US20090108251A1 (en) * 2005-04-25 2009-04-30 Mohammad Shafiqul Kabir Controlled growth of a nanostructure on a substrate
US7977761B2 (en) 2005-04-25 2011-07-12 Smoltek Ab Controlled growth of a nanostructure on a substrate, and electron emission devices based on the same
US20060292716A1 (en) * 2005-06-27 2006-12-28 Lsi Logic Corporation Use selective growth metallization to improve electrical connection between carbon nanotubes and electrodes
US8415787B2 (en) 2005-08-26 2013-04-09 Smoltek Ab Integrated circuits having interconnects and heat dissipators based on nanostructures
US8183659B2 (en) 2005-08-26 2012-05-22 Smoltek Ab Integrated circuits having interconnects and heat dissipators based on nanostructures
US20070096304A1 (en) * 2005-08-26 2007-05-03 Kabir Mohammad S Interconnects and heat dissipators based on nanostructures
US7777291B2 (en) 2005-08-26 2010-08-17 Smoltek Ab Integrated circuits having interconnects and heat dissipators based on nanostructures
US20100328898A1 (en) * 2005-08-26 2010-12-30 Smoltek Ab Integrated Circuits Having Interconnects and Heat Dissipators Based on Nanostructures
US20100264544A1 (en) * 2006-01-20 2010-10-21 Jang-Eun Heo Device including contact structure and method of forming the same
US7982318B2 (en) * 2006-01-20 2011-07-19 Samsung Electronics Co., Ltd. Device including contact structure and method of forming the same
US20080095937A1 (en) * 2006-05-18 2008-04-24 California Institute Of Technology Robust filament assembly for a hot-wire chemical vapor deposition system
US7727590B2 (en) * 2006-05-18 2010-06-01 California Institute Of Technology Robust filament assembly for a hot-wire chemical vapor deposition system
US20080096293A1 (en) * 2006-10-24 2008-04-24 Ephraim Suhir Method and Apparatus for Evaluation and Improvement of Mechanical and Thermal Properties of CNT/CNF Arrays
US8048688B2 (en) 2006-10-24 2011-11-01 Samsung Electronics Co., Ltd. Method and apparatus for evaluation and improvement of mechanical and thermal properties of CNT/CNF arrays
DE102008004183A1 (en) 2007-01-12 2008-07-31 Samsung Electronics Co., Ltd., Suwon Integrated circuit device has several carbon nanotubes that are formed in opening of insulation layer so that nanotubes are electrically connected to copper pattern through catalyst metal layer and barrier layer
US20080246148A1 (en) * 2007-01-12 2008-10-09 Samsung Electronics Co., Ltd. Electrical Interconnect Structures Having Carbon Nanotubes Therein and Methods of Forming Same
US7897529B2 (en) 2007-03-23 2011-03-01 Lydall, Inc. Substrate for carrying catalytic particles
US20080246149A1 (en) * 2007-04-06 2008-10-09 Hynix Semiconductor Inc. Semiconductor device and method for forming device isolation film of semiconductor device
FR2917894A1 (en) * 2007-06-22 2008-12-26 Commissariat Energie Atomique Catalyst locating method for microelectronic industry, involves filling opening with filling material after depositing catalyst on upper surface of layer, removing catalyst deposited on surface, and removing filling material
EP2197782A4 (en) * 2007-09-12 2017-11-15 Smoltek AB Connecting and bonding adjacent layers with nanostructures
TWI511208B (en) * 2007-09-12 2015-12-01 Smoltek Ab Connecting and bonding adjacent layers with nanostructures
US20090072408A1 (en) * 2007-09-12 2009-03-19 Smoltek Ab Connecting and Bonding Adjacent Layers with Nanostructures
WO2009035393A1 (en) 2007-09-12 2009-03-19 Smoltek Ab Connecting and bonding adjacent layers with nanostructures
KR101487346B1 (en) 2007-09-12 2015-01-28 스몰텍 에이비 Connecting and Bonding Adjacent Layers with Nanostructures
US8106517B2 (en) * 2007-09-12 2012-01-31 Smoltek Ab Connecting and bonding adjacent layers with nanostructures
US8815332B2 (en) 2007-09-12 2014-08-26 Smoltek Ab Connecting and bonding adjacent layers with nanostructures
US8253253B2 (en) 2007-09-12 2012-08-28 Smoltek Ab Connecting and bonding adjacent layers with nanostructures
US8709941B2 (en) * 2007-12-21 2014-04-29 Advanced Micro Devices, Inc. Method for forming contact in an integrated circuit
US20090159985A1 (en) * 2007-12-21 2009-06-25 Advanced Micro Devices, Inc. Integrated circuit system with contact integration
US8283786B2 (en) * 2007-12-21 2012-10-09 Advanced Micro Devices, Inc. Integrated circuit system with contact integration
US8866307B2 (en) 2008-02-25 2014-10-21 Smoltek Ab Deposition and selective removal of conducting helplayer for nanostructure processing
US20090233124A1 (en) * 2008-02-25 2009-09-17 Smoltek Ab Deposition and Selective Removal of Conducting Helplayer for Nanostructure Processing
US8508049B2 (en) 2008-02-25 2013-08-13 Smoltek Ab Deposition and selective removal of conducting helplayer for nanostructure processing
US9114993B2 (en) 2008-02-25 2015-08-25 Smoltek Ab Deposition and selective removal of conducting helplayer for nanostructure processing
US20100327444A1 (en) * 2008-02-29 2010-12-30 Fujitsu Limited Sheet structure, semiconductor device and method of growing carbon structure
US8350391B2 (en) 2008-02-29 2013-01-08 Fujitsu Limited Sheet structure, semiconductor device and method of growing carbon structure
US8258060B2 (en) 2008-02-29 2012-09-04 Fujitsu Limited Sheet structure, semiconductor device and method of growing carbon structure
CN101959788A (en) * 2008-02-29 2011-01-26 富士通株式会社 Sheet structure, semiconductor device and method of growing carbon structure
US20110240349A1 (en) * 2008-09-22 2011-10-06 Lakshmi Supriya Multiple die structure and method of forming a connection between first and second dies in same
JP2012528937A (en) * 2009-06-02 2012-11-15 フラウンホッファー−ゲゼルシャフト ツァ フェルダールング デァ アンゲヴァンテン フォアシュンク エー.ファオ Coating apparatus and coating method
CN102803557A (en) * 2009-06-02 2012-11-28 费劳恩霍夫应用研究促进协会 Coating installation and coating method
US20100313951A1 (en) * 2009-06-10 2010-12-16 Applied Materials, Inc. Carbon nanotube-based solar cells
US8747942B2 (en) * 2009-06-10 2014-06-10 Applied Materials, Inc. Carbon nanotube-based solar cells
US9099537B2 (en) 2009-08-28 2015-08-04 International Business Machines Corporation Selective nanotube growth inside vias using an ion beam
CN102484096A (en) * 2009-08-28 2012-05-30 国际商业机器公司 Selective nanotube growth inside vias using an ion beam
GB2485486B (en) * 2009-08-28 2013-10-30 Ibm Selective nanotube growth inside vias using an ion beam
DE112010003451B4 (en) * 2009-08-28 2015-01-22 International Business Machines Corporation Selective growth of a single nanotube within a via using an ion beam
US20110048930A1 (en) * 2009-08-28 2011-03-03 International Business Machines Corporation Selective nanotube growth inside vias using an ion beam
TWI474973B (en) * 2009-08-28 2015-03-01 Ibm Selective nanotube growth inside vias using an ion beam
WO2011023519A1 (en) * 2009-08-28 2011-03-03 International Business Machines Corporation Selective nanotube growth inside vias using an ion beam
GB2485486A (en) * 2009-08-28 2012-05-16 Ibm Selective nanotube growth inside vias using an ion beam
US9112002B2 (en) * 2012-02-13 2015-08-18 Tyco Electronics Corporation Electrical conductors and methods of manufacturing electrical conductors
US20130206461A1 (en) * 2012-02-13 2013-08-15 Tyco Electronics Corporation Electrical Conductors and Methods of Manufacturing Electrical Conductors
US9024436B2 (en) * 2013-06-19 2015-05-05 Broadcom Corporation Thermal interface material for integrated circuit package
US20140374897A1 (en) * 2013-06-19 2014-12-25 Broadcom Corporation Thermal interface material for integrated circuit package and method of making the same
CN105226006A (en) * 2014-06-12 2016-01-06 中芯国际集成电路制造(上海)有限公司 The formation method of interconnection structure
CN111470468A (en) * 2020-04-22 2020-07-31 华中科技大学 Method for transferring vertical carbon nano tube to target substrate

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