GB2312439A - Plasma enhanced chemical vapour deposition of a layer - Google Patents
Plasma enhanced chemical vapour deposition of a layer Download PDFInfo
- Publication number
- GB2312439A GB2312439A GB9608565A GB9608565A GB2312439A GB 2312439 A GB2312439 A GB 2312439A GB 9608565 A GB9608565 A GB 9608565A GB 9608565 A GB9608565 A GB 9608565A GB 2312439 A GB2312439 A GB 2312439A
- Authority
- GB
- United Kingdom
- Prior art keywords
- layer
- substrate
- electrode
- silicon
- vapour deposition
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C23—COATING 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
- C23C—COATING 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
- C23C16/00—Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes
- C23C16/44—Chemical 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 method of coating
- C23C16/50—Chemical 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 method of coating using electric discharges
- C23C16/505—Chemical 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 method of coating using electric discharges using radio frequency discharges
- C23C16/509—Chemical 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 method of coating using electric discharges using radio frequency discharges using internal electrodes
- C23C16/5096—Flat-bed apparatus
-
- C—CHEMISTRY; METALLURGY
- C23—COATING 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
- C23C—COATING 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
- C23C16/00—Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes
- C23C16/22—Chemical 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
- C23C16/30—Deposition of compounds, mixtures or solid solutions, e.g. borides, carbides, nitrides
- C23C16/40—Oxides
- C23C16/401—Oxides containing silicon
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- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Physics & Mathematics (AREA)
- Plasma & Fusion (AREA)
- Optical Integrated Circuits (AREA)
Abstract
A layer which is suitable for use in a planar waveguide optical circuit is formed on a substrate by plasma enhanced chemical vapour deposition, the process being carried out in a chamber having two electrodes. One of the electrodes carries the substrate and is energised with an electrical signal at a radio frequency through a capacitor. The other electrode is held at ground potential. The substrate is maintained electrically negative with respect to earth (50 - 500 volts). Silicon and germanium compounds with hydrogen ; or silicon, germanium, phosphorus and boron compounds with hydrogen are fed to the chamber with nitrous oxide.
Description
PLASMA ENHANCED CHEMICAL VAPOUR
DEPOSITION OF A LAYER
The present invention concerns the production of a layer, which is suitable for use as the core of a planar waveguide optical circuit using plasma enhanced chemical vapour deposition (PECVD). The production of a silicon oxide layer is described, as an example, although layers of other materials may be deposited, and the method to be described may be used for the production of layers which are suitable for other applications than planar waveguides devices.
Normally a deposit of silicon oxide or other materials, requires extensive annealing and densification of the layer deposited, the latter serving to expel hydrogen, water or hydrides, and then the compaction of the newly deposited layer to render it suitable for use in a planar waveguide. An arrangement to be described below seeks to reduce the typical requirement for annealing and densification, at least in part.
In the arrangement to be described below there is disclosed the use of an r.f. source between the electrodes of a plasma chamber, the electrode associated with a target substrate being energized through a capacitor, and the other electrode being directly earthed. It has previously been proposed to provide the energisation, for a plasma used in an enhanced chemical vapour deposition (PECVD) process, live, through a capacitor, to the electrode which is opposite to that supporting the substrate arranged to receive the deposit, with the aim, it is believed, of providing a more stable layer. By means of the arrangement to be described below, as an example, a more desirable layer is obtained, probably as a result of the bombardment of the layer by positive ions derived from the plasma discharge.
An electrode carrying a substrate, e.g. a silicon single crystal substrate and a buffer SiO2, is made alternately positive and negative, relative to an earthed, electrode in the arrangement to be described, so that the more mobile electrons travel in greater quantities during a half cycle of one polarity to the live electrode than do the less mobile positive ions during a half cycle of other polarity of an applied r.f. signal. Thus the live electrode may acquire a negative charge of, for example some -500 volts. This it is believed adds to the bombardment energy by which the positive ions originating from the plasma materials impact the target substrate. The resulting deposited layer of germania doped SiO2 is made more dense to a considerable extent.
An arrangement illustrative of the invention will now be described, by way of example, with reference to the single figure of the accompanying drawing which shows diagrammatically parts of a
PECVD chamber.
Referring to the drawing, there is shown a plasma discharge chamber 1 which has an inlet 2 for precursor materials such as silane, nitrous oxide, germane, diborane, phosphine or other sources of silica, boron phosphorus or germanium doping, and an outlet 3 for pumping-out spent or exhaust materials. A source 4 of power in the radio frequency band which may, for example, be between 50 kHz and 13.5 MHz, is applied to an electrode 5 carrying a substrate 6 with a buffer layer for receiving a core layer deposit for use in a planar waveguide. The r.f. power is applied to the electrode 5 through a capacitor 7 which is able to withstand several hundred direct volts and to pass the r.f. power. A second electrode 8 is earthed: Upon the initiation of a plasma discharge between the electrodes 5 and 8 through the ionized precursor material, a germanium doped silicon oxide layer is formed on the substrate 6. The silicon oxide layer formed in this way is in a very satisfactorily impacted form, and has a very satisfactorily repeatable, or selectable, refractive index, which is most important in precursor wave guide work, particularly for interfacing with fibre optics or wavelength division multiplexing, which involves closely controlled differences between > 's of neighbouring layers. The negative voltage developed at the live electrode 5 may be between 50-500 volts.
It will be understood that, although the invention has been illustrated, by way of example, with reference to one particular arrangement, variations and modifications thereof, as well as other embodiments may be made within the scope of the protection sought.
For example, although the method has been described with reference to the production of a layer which is suitable for use in a waveguide, a layer produced by the method may have other applications, and the layer may be other than a silicon oxide layer.
Claims (8)
1. A method of depositing a layer by PECVD which layer is to form part of an optical waveguide, wherein the substrate is maintained electrically negative with respect to ground.
2. A method of depositing a layer which is suitable for use in a planar waveguide optical circuit and which is carried out in a chamber having two electrodes using plasma enhanced chemical vapour deposition, including the step of energising an electrode associated with a substrate for the layer through a capacitor by means of an electrical signal at a radio frequency, the second electrode being held at ground potential.
3. A method as claimed in claim 1 or 2 wherein silicon and germanium compounds with hydrogen, or silicon, germanium phosphorus and boron compounds with hydrogen, are fed to the chamber with nitrous oxide.
4. A method as claimed in either claim 1, 2 or claim 3 wherein the r.f. source provides a signal at a frequency between 50 kHz and 13.5 MHz.
5. A method as claimed in any one of the preceding claims wherein a voltage between approximately 50-500 volts negative is developed during operation at the electrode to which the r.f. signal is capacitively fed with respect to the second electrode.
6. A method as claimed in any one of the preceding claims wherein the substrate includes silicon or quartz.
7. A method as claimed in claim 1 substantially as described herein with reference to the single figure of the accompanying drawing.
8. A layer deposited on a substrate by the method of any one of the preceding claims.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB9608565A GB2312439A (en) | 1996-04-24 | 1996-04-24 | Plasma enhanced chemical vapour deposition of a layer |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB9608565A GB2312439A (en) | 1996-04-24 | 1996-04-24 | Plasma enhanced chemical vapour deposition of a layer |
Publications (2)
Publication Number | Publication Date |
---|---|
GB9608565D0 GB9608565D0 (en) | 1996-07-03 |
GB2312439A true GB2312439A (en) | 1997-10-29 |
Family
ID=10792617
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB9608565A Withdrawn GB2312439A (en) | 1996-04-24 | 1996-04-24 | Plasma enhanced chemical vapour deposition of a layer |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB2312439A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7080528B2 (en) | 2002-10-23 | 2006-07-25 | Applied Materials, Inc. | Method of forming a phosphorus doped optical core using a PECVD process |
WO2015034653A1 (en) * | 2013-09-06 | 2015-03-12 | Applied Materials, Inc. | Pecvd microcrystalline silicon germanium (sige) |
CN106783542A (en) * | 2016-12-23 | 2017-05-31 | 苏州工业园区纳米产业技术研究院有限公司 | The method that LPCVD methods deposit germanium-silicon film |
Citations (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4060660A (en) * | 1976-01-15 | 1977-11-29 | Rca Corporation | Deposition of transparent amorphous carbon films |
US4681653A (en) * | 1984-06-01 | 1987-07-21 | Texas Instruments Incorporated | Planarized dielectric deposited using plasma enhanced chemical vapor deposition |
GB2194556A (en) * | 1986-08-21 | 1988-03-09 | Special Research Systems Limit | Plasma enhanced chemical vapour deposition of films |
EP0448227A1 (en) * | 1990-02-21 | 1991-09-25 | Ngk Insulators, Ltd. | Composite materials and a process for producing the same |
US5052339A (en) * | 1990-10-16 | 1991-10-01 | Air Products And Chemicals, Inc. | Radio frequency plasma enhanced chemical vapor deposition process and reactor |
US5120680A (en) * | 1990-07-19 | 1992-06-09 | At&T Bell Laboratories | Method for depositing dielectric layers |
EP0536664A1 (en) * | 1991-10-07 | 1993-04-14 | Sumitomo Metal Industries, Ltd. | A method for forming a thin film |
GB2270326A (en) * | 1992-09-03 | 1994-03-09 | Kobe Steel Europ Ltd | Growth of diamond films on silicon substrates with application of bias to substrate; tessellated patterns |
US5312778A (en) * | 1989-10-03 | 1994-05-17 | Applied Materials, Inc. | Method for plasma processing using magnetically enhanced plasma chemical vapor deposition |
EP0686708A1 (en) * | 1993-02-24 | 1995-12-13 | OHMI, Tadahiro | Film forming method and film forming apparatus |
GB2291652A (en) * | 1994-07-23 | 1996-01-31 | Barr & Stroud Ltd | Protective coating of gallium phosphide for optical components |
-
1996
- 1996-04-24 GB GB9608565A patent/GB2312439A/en not_active Withdrawn
Patent Citations (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4060660A (en) * | 1976-01-15 | 1977-11-29 | Rca Corporation | Deposition of transparent amorphous carbon films |
US4681653A (en) * | 1984-06-01 | 1987-07-21 | Texas Instruments Incorporated | Planarized dielectric deposited using plasma enhanced chemical vapor deposition |
GB2194556A (en) * | 1986-08-21 | 1988-03-09 | Special Research Systems Limit | Plasma enhanced chemical vapour deposition of films |
US5312778A (en) * | 1989-10-03 | 1994-05-17 | Applied Materials, Inc. | Method for plasma processing using magnetically enhanced plasma chemical vapor deposition |
EP0448227A1 (en) * | 1990-02-21 | 1991-09-25 | Ngk Insulators, Ltd. | Composite materials and a process for producing the same |
US5120680A (en) * | 1990-07-19 | 1992-06-09 | At&T Bell Laboratories | Method for depositing dielectric layers |
US5052339A (en) * | 1990-10-16 | 1991-10-01 | Air Products And Chemicals, Inc. | Radio frequency plasma enhanced chemical vapor deposition process and reactor |
EP0536664A1 (en) * | 1991-10-07 | 1993-04-14 | Sumitomo Metal Industries, Ltd. | A method for forming a thin film |
GB2270326A (en) * | 1992-09-03 | 1994-03-09 | Kobe Steel Europ Ltd | Growth of diamond films on silicon substrates with application of bias to substrate; tessellated patterns |
EP0686708A1 (en) * | 1993-02-24 | 1995-12-13 | OHMI, Tadahiro | Film forming method and film forming apparatus |
GB2291652A (en) * | 1994-07-23 | 1996-01-31 | Barr & Stroud Ltd | Protective coating of gallium phosphide for optical components |
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7080528B2 (en) | 2002-10-23 | 2006-07-25 | Applied Materials, Inc. | Method of forming a phosphorus doped optical core using a PECVD process |
US7325419B2 (en) | 2002-10-23 | 2008-02-05 | Applied Materials, Inc. | Method of forming a phosphorus doped optical core using a PECVD process |
US7383702B2 (en) | 2002-10-23 | 2008-06-10 | Applied Materials, Inc. | Method of forming a phosphorus doped optical core using a PECVD process |
WO2015034653A1 (en) * | 2013-09-06 | 2015-03-12 | Applied Materials, Inc. | Pecvd microcrystalline silicon germanium (sige) |
CN105492657A (en) * | 2013-09-06 | 2016-04-13 | 应用材料公司 | Pecvd microcrystalline silicon germanium (SIGE) |
US9484199B2 (en) | 2013-09-06 | 2016-11-01 | Applied Materials, Inc. | PECVD microcrystalline silicon germanium (SiGe) |
CN105492657B (en) * | 2013-09-06 | 2018-07-10 | 应用材料公司 | PECVD crystallites SiGe (SIGE) |
CN106783542A (en) * | 2016-12-23 | 2017-05-31 | 苏州工业园区纳米产业技术研究院有限公司 | The method that LPCVD methods deposit germanium-silicon film |
Also Published As
Publication number | Publication date |
---|---|
GB9608565D0 (en) | 1996-07-03 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
WAP | Application withdrawn, taken to be withdrawn or refused ** after publication under section 16(1) |