WO2017190277A1 - Doped anatase titanium dioxide material, preparation method therefor and use thereof - Google Patents
Doped anatase titanium dioxide material, preparation method therefor and use thereof Download PDFInfo
- Publication number
- WO2017190277A1 WO2017190277A1 PCT/CN2016/080924 CN2016080924W WO2017190277A1 WO 2017190277 A1 WO2017190277 A1 WO 2017190277A1 CN 2016080924 W CN2016080924 W CN 2016080924W WO 2017190277 A1 WO2017190277 A1 WO 2017190277A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- titanium dioxide
- anatase titanium
- dioxide material
- doped
- doped anatase
- Prior art date
Links
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 title claims abstract description 98
- 239000000463 material Substances 0.000 title claims abstract description 80
- 238000002360 preparation method Methods 0.000 title description 9
- 239000010936 titanium Substances 0.000 claims abstract description 55
- 229910052738 indium Inorganic materials 0.000 claims abstract description 21
- 238000005245 sintering Methods 0.000 claims abstract description 15
- 229910052758 niobium Inorganic materials 0.000 claims abstract description 10
- 229910052796 boron Inorganic materials 0.000 claims abstract description 6
- 239000000126 substance Substances 0.000 claims abstract description 5
- 229910052782 aluminium Inorganic materials 0.000 claims abstract description 4
- 229910052797 bismuth Inorganic materials 0.000 claims abstract description 4
- 229910052733 gallium Inorganic materials 0.000 claims abstract description 4
- 229910052715 tantalum Inorganic materials 0.000 claims abstract description 4
- 229910052721 tungsten Inorganic materials 0.000 claims abstract description 4
- 229910052720 vanadium Inorganic materials 0.000 claims abstract description 4
- 238000006243 chemical reaction Methods 0.000 claims description 32
- 239000000919 ceramic Substances 0.000 claims description 23
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 22
- 229910052719 titanium Inorganic materials 0.000 claims description 19
- 238000000034 method Methods 0.000 claims description 12
- 150000002500 ions Chemical class 0.000 claims description 10
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims description 9
- 239000003985 ceramic capacitor Substances 0.000 claims description 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 9
- 239000007810 chemical reaction solvent Substances 0.000 claims description 8
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 claims description 6
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims description 6
- 239000007795 chemical reaction product Substances 0.000 claims description 5
- 238000010438 heat treatment Methods 0.000 claims description 5
- 150000004677 hydrates Chemical class 0.000 claims description 5
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 claims description 4
- 238000002156 mixing Methods 0.000 claims description 3
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 claims description 2
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 claims description 2
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 claims description 2
- 239000005642 Oleic acid Substances 0.000 claims description 2
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 claims description 2
- 238000004090 dissolution Methods 0.000 claims description 2
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 claims description 2
- 239000007788 liquid Substances 0.000 claims description 2
- 239000000203 mixture Substances 0.000 claims description 2
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 claims description 2
- 238000011403 purification operation Methods 0.000 claims description 2
- 230000035484 reaction time Effects 0.000 claims description 2
- 238000000926 separation method Methods 0.000 claims description 2
- 238000005406 washing Methods 0.000 claims description 2
- APFVFJFRJDLVQX-UHFFFAOYSA-N indium atom Chemical compound [In] APFVFJFRJDLVQX-UHFFFAOYSA-N 0.000 description 8
- 239000002086 nanomaterial Substances 0.000 description 8
- 239000004408 titanium dioxide Substances 0.000 description 7
- -1 europium ions Chemical class 0.000 description 6
- 229910052684 Cerium Inorganic materials 0.000 description 5
- 239000002994 raw material Substances 0.000 description 5
- 238000010586 diagram Methods 0.000 description 4
- 229910010413 TiO 2 Inorganic materials 0.000 description 3
- VMPVEPPRYRXYNP-UHFFFAOYSA-I antimony(5+);pentachloride Chemical compound Cl[Sb](Cl)(Cl)(Cl)Cl VMPVEPPRYRXYNP-UHFFFAOYSA-I 0.000 description 3
- 238000001354 calcination Methods 0.000 description 3
- 238000005119 centrifugation Methods 0.000 description 3
- 238000001816 cooling Methods 0.000 description 3
- VBXWCGWXDOBUQZ-UHFFFAOYSA-K diacetyloxyindiganyl acetate Chemical compound [In+3].CC([O-])=O.CC([O-])=O.CC([O-])=O VBXWCGWXDOBUQZ-UHFFFAOYSA-K 0.000 description 3
- 238000001453 impedance spectrum Methods 0.000 description 3
- 229910052746 lanthanum Inorganic materials 0.000 description 3
- FZLIPJUXYLNCLC-UHFFFAOYSA-N lanthanum atom Chemical compound [La] FZLIPJUXYLNCLC-UHFFFAOYSA-N 0.000 description 3
- 239000010410 layer Substances 0.000 description 3
- 239000002245 particle Substances 0.000 description 3
- 239000002356 single layer Substances 0.000 description 3
- XJDNKRIXUMDJCW-UHFFFAOYSA-J titanium tetrachloride Chemical compound Cl[Ti](Cl)(Cl)Cl XJDNKRIXUMDJCW-UHFFFAOYSA-J 0.000 description 3
- 229910052693 Europium Inorganic materials 0.000 description 2
- 238000001237 Raman spectrum Methods 0.000 description 2
- 238000003917 TEM image Methods 0.000 description 2
- 239000003990 capacitor Substances 0.000 description 2
- 239000013078 crystal Substances 0.000 description 2
- 239000003989 dielectric material Substances 0.000 description 2
- 229910021645 metal ion Inorganic materials 0.000 description 2
- 229920006395 saturated elastomer Polymers 0.000 description 2
- 238000001228 spectrum Methods 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 238000002441 X-ray diffraction Methods 0.000 description 1
- 229910052787 antimony Inorganic materials 0.000 description 1
- WATWJIUSRGPENY-UHFFFAOYSA-N antimony atom Chemical compound [Sb] WATWJIUSRGPENY-UHFFFAOYSA-N 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 229910010293 ceramic material Inorganic materials 0.000 description 1
- GWXLDORMOJMVQZ-UHFFFAOYSA-N cerium Chemical compound [Ce] GWXLDORMOJMVQZ-UHFFFAOYSA-N 0.000 description 1
- 230000036571 hydration Effects 0.000 description 1
- 238000006703 hydration reaction Methods 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 230000010354 integration Effects 0.000 description 1
- 238000003475 lamination Methods 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 230000015654 memory Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 239000011858 nanopowder Substances 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 238000009738 saturating Methods 0.000 description 1
- 238000004626 scanning electron microscopy Methods 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01G—COMPOUNDS CONTAINING METALS NOT COVERED BY SUBCLASSES C01D OR C01F
- C01G23/00—Compounds of titanium
- C01G23/04—Oxides; Hydroxides
- C01G23/047—Titanium dioxide
- C01G23/053—Producing by wet processes, e.g. hydrolysing titanium salts
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B35/00—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
- C04B35/01—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics
- C04B35/46—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics based on titanium oxides or titanates
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B35/00—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
- C04B35/622—Forming processes; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
- C04B35/64—Burning or sintering processes
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01G—CAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES, LIGHT-SENSITIVE OR TEMPERATURE-SENSITIVE DEVICES OF THE ELECTROLYTIC TYPE
- H01G4/00—Fixed capacitors; Processes of their manufacture
- H01G4/002—Details
- H01G4/018—Dielectrics
- H01G4/06—Solid dielectrics
- H01G4/08—Inorganic dielectrics
- H01G4/12—Ceramic dielectrics
Definitions
- the invention relates to a doped anatase titanium dioxide material, a preparation method thereof and an application thereof.
- bimetallic ion co-doped titanium dioxide is attracting widespread attention due to its unique dielectric properties.
- indium and lanthanum co-doped titania ceramics have a dielectric constant of more than 10 4 and a dielectric loss of less than 0.05.
- excellent dielectric properties can be maintained over a wide temperature range (from -180 ° C to 200 ° C).
- Other trivalent ions and cerium co-doped titanium dioxide ceramic materials also exhibit the same dielectric properties of indium and lanthanum co-doped titanium dioxide ceramics.
- indium and lanthanum co-doped titanium dioxide films also have high dielectric constant and low dielectric loss over a wide frequency range. Divalent europium ions and pentavalent europium ions are also co-doped into the titanium dioxide ceramic matrix, and their dielectric properties have also received extensive attention.
- the sintering temperature of the commonly used doped titanium dioxide dielectric material is generally around 1400 ° C, and the sintering temperature is high.
- One doping anatase titanium dioxide material through the chemical formula of the doped anatase titanium dioxide material is (A x B y) Ti 1-3 / 4x-5 / 4y O 2, wherein, A is selected from Bi, At least one of In, Ga, and Al, and B is at least one selected from the group consisting of Nb, W, V, and Ta, and 0 ⁇ x ⁇ 0.10, 0 ⁇ y ⁇ 0.10.
- the preparation method of the doped anatase titanium dioxide material comprises the following steps:
- the A source containing trivalent A and the B source containing pentavalent B are added to the premix and stirred until the source A and the source B are completely dissolved to form a reaction solution in which A 3+ and Ti 4+ are present.
- the molar ratio is n
- the molar ratio of B 5+ to Ti 4+ is m, wherein 0 ⁇ n ⁇ 2, 0 ⁇ m ⁇ 2; the reaction solution is fully reacted at 50 ° C to 250 ° C to obtain the blend Miscellaneous anatase titanium dioxide material.
- the above doped anatase titanium dioxide material is chemically modified with anatase titanium dioxide by co-doping + trivalent and +5 valent metal ions, and the modified doped anatase titanium dioxide material has a giant dielectric property and can be directly used for
- a high dielectric single-layer or multi-layer ceramic capacitor is prepared, and the doped anatase titanium dioxide material is used as a raw material to directly sinter the corresponding ceramic, and the calcination temperature only needs about 1000 ° C, and the sintering temperature is low.
- Example 3 is a transmission electron micrograph of the doped anatase titanium dioxide material prepared in Example 1;
- Example 4 is an XPS diagram of the doped anatase titanium dioxide material prepared in Example 1;
- Example 5 is a room temperature dielectric spectrum diagram of a ceramic made of the doped anatase titanium dioxide material prepared in Example 1.
- the method, the ceramic made of the doped anatase titanium dioxide material and the doped anatase titanium dioxide material are further described in detail in the ceramic capacitor.
- the chemical formula of the doped anatase titanium dioxide material of one embodiment is (A x B y )Ti 1-3/4x-5/4y O 2 , wherein A is at least selected from the group consisting of Bi, In, Ga, and Al.
- B is at least one selected from the group consisting of Nb, W, V, and Ta, and 0 ⁇ x ⁇ 0.10, 0 ⁇ y ⁇ 0.10.
- the doped anatase titanium dioxide material has a dimension in the one-dimensional direction of less than 100 nm.
- the doped anatase titanium dioxide material contains Ti 3+ ions induced by B 5+ ion doping.
- the ceramic prepared from the doped anatase titanium dioxide material has a dielectric loss of less than 0.15.
- the ceramic prepared from the doped anatase titanium dioxide material has a dielectric constant in the range of 20 Hz to 10 5 Hz of 8,000 to 150,000.
- the above doped anatase titanium dioxide material is chemically modified with anatase titanium dioxide by co-doping + trivalent and +5 valent metal ions, and the modified doped anatase titanium dioxide material has a giant dielectric property and can be directly used for
- a high dielectric single-layer or multi-layer ceramic capacitor is prepared, and the doped anatase titanium dioxide material is used as a raw material to directly sinter the corresponding ceramic, the calcination temperature only needs about 1000 ° C, and the sintering temperature is low; the size of the doped anatase titanium dioxide material Smaller, as a raw material of ceramic capacitors, it can realize the miniaturization of electronic devices and the integration of its production process, which can reduce the calcination temperature in the molding process, reduce the thickness of each dielectric film, and increase the energy density of ceramic devices.
- This small nanomaterial can promote the miniaturization of multilayer ceramic capacitors with high capacitance and excellent temperature stability.
- the preparation method of the above doped anatase titanium dioxide material comprises the following steps:
- Step S110 mixing a titanium source containing tetravalent titanium with a reaction solvent to form a premixed solution, wherein the concentration of Ti 4+ in the premixed solution is 0.0005 mol/L to a concentration of Ti 4+ saturated.
- Saturating the concentration of Ti 4+ means that the titanium source reaches saturation solubility in the reaction solvent.
- the titanium source is selected from the group consisting of Ti(NO 3 ) 4 , a hydrate of Ti(NO 3 ) 4 , a hydrate of TiCl 4 , TiCl 4 , a hydrate of Ti(SO 4 ) 2 , Ti(SO 4 ) 2 , Hydrate of TiOSO 4 , TiOSO 4 , hydrate of C 8 H 20 O 4 Ti, C 8 H 20 O 4 Ti, hydrate of C 12 H 28 O 4 Ti, C 12 H 28 O 4 Ti, C 16 H At least one of a hydrate of 36 O 4 Ti and C 16 H 36 O 4 Ti.
- the reaction solvent is at least one selected from the group consisting of water, ethanol, methanol, isopropanol, acetone, and oleic acid.
- the volume of the reaction solvent is greater than 5 ml.
- step S120 the A source containing trivalent A and the B source containing pentavalent B are added to the premixed solution and stirred until the source A and the source B are completely dissolved to form a reaction solution.
- the amount of the A source containing trivalent A and the B source containing pentavalent B is determined according to the preset concentration of A 3+ and B 5+ in the reaction solution.
- the source of A is selected from the group consisting of hydrates of A(NO 3 ) 3 , A(NO 3 ) 3 , hydrates of ACl 3 , ACl 3 , hydration of A 2 (SO 4 ) 3 , A 2 (SO 4 ) 3 At least one of a hydrate of A(C 2 H 3 O 2 ) 3 and A(C 2 H 3 O 2 ) 3 .
- the B source is selected from the group consisting of hydrates of B(NO 3 ) 5 , B(NO 3 ) 5 , hydrates of B 2 (SO 4 ) 5 , B 2 (SO 4 ) 5 , hydrate of BCl 5 and BCl 5 . At least one of the substances.
- the stirring is carried out at normal temperature.
- the stirring time is from 0 hours to 10 hours, preferably 1.5 hours.
- Step S130 the reaction solution is sufficiently reacted at 50 ° C to 250 ° C to obtain a doped anatase titanium dioxide material.
- the reaction time is 4 hours or more.
- the reaction solution is sufficiently reacted at 50 ° C to 250 ° C to be separated and purified to obtain a doped anatase titanium dioxide material.
- the separation and purification operation is specifically: separately washing the obtained reaction product with water and ethanol and centrifuging.
- the reaction solution is contained in a sealed reaction vessel, and the reaction vessel is heated in a heating apparatus at 50 ° C to 250 ° C.
- the heating device is at least one of an oven, a water bath, and an oil bath. kind.
- Synthesis-doped anatase titanium dioxide material is simple, mild reaction conditions; non-toxic raw materials and reaction by-products, more environmentally friendly; doped anatase titanium dioxide material prepared has a smaller particle size; and by changing the A 3+ The concentration of B 5+ ions in the reaction solvent can be adjusted to the co-doping concentration in the doped anatase titanium dioxide material.
- the ceramic of one embodiment is formed by sintering the above-doped anatase titanium dioxide material.
- the sintering temperature is below 1200 °C. More preferably, the sintering temperature is from 1000 ° C to 1200 ° C.
- the doped anatase titanium dioxide material is pressed into a green body and the green body is sintered.
- the sintering is carried out in a high temperature furnace
- the sintering time is from 0.5 hours to 60 hours.
- the above ceramics have high dielectric properties and a low sintering temperature.
- the above doped anatase titanium dioxide material can be applied in the fields of ceramic capacitors, biosensors, dye-sensitized cells, and organic-inorganic hybrid materials.
- the doped anatase titanium dioxide material particles directly as a raw material of a single-layer or multi-layer ceramic capacitor can also effectively increase the number of laminations per unit thickness, thereby increasing the storage density of the capacitor device.
- the preparation process is as follows:
- the preparation process is as follows:
- the preparation process is as follows:
- FIG. 1 is an embodiment 1 (5 at.% In 3+ and 5 at.% Nb 5+ ), Example 2 (3 at.% In 3+ and 3 at.% Nb 5+ ), and Example 3 ( XRD patterns of doped anatase titanium dioxide materials prepared by 1 at. % In 3 + and 1 at. % Nb 5+ ). It can be seen from Fig. 1 that the synthesized indium and cerium ion co-doped TiO 2 nanomaterials have an anatase crystal structure, and also demonstrate that the doped anatase titanium dioxide materials prepared in Examples 1-3 have a single phase characteristic and do not contain other Impurities.
- FIG. 2 is Embodiment 1 (5 at.% In 3+ and 5 at.% Nb 5+ ), Example 2 (3 at.% In 3+ and 3 at.% Nb 5+ ), and Example 3 ( Raman spectra of doped anatase titanium dioxide material prepared at 1 at.%In 3+ and 1 at.% Nb 5+ ) at room temperature. It can be seen from Fig. 2 that the synthesized indium and cerium ion co-doped TiO 2 nanomaterials have an anatase crystal structure.
- FIG. 3 is a transmission electron micrograph of the doped anatase titanium dioxide material prepared in Example 1. It can be seen from Fig. 3 that the synthesized indium and cerium ion co-doped TiO 2 nanomaterials have a particle size of about 10 nm.
- FIG. 4 is an XPS diagram of the doped anatase titanium dioxide material prepared in Example 1. It can be seen from Fig. 4 that the synthesized indium and cerium ion co-doped titanium dioxide nanomaterials contain Ti 3+ ions.
- FIG. 5 is a room temperature dielectric spectrum diagram of a ceramic made of the doped anatase titanium dioxide material prepared in Example 1.
- the room temperature dielectric spectrum indicates that the ceramic prepared using the nanopowder has a high dielectric constant (8000-150000) in the range of 20 Hz to 10 5 Hz and a dielectric loss of less than 0.15.
- Table 1 shows the energy spectrum (EDS) of the doped anatase titanium dioxide materials prepared in Examples 1 to 3. The EDS results were directly tested by scanning electron microscopy.
- indium and antimony doped ions are indeed present in the doped anatase titanium dioxide material prepared in Examples 1 to 3, and the concentration of the doping ions can be regulated in the sample.
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Ceramic Engineering (AREA)
- Manufacturing & Machinery (AREA)
- Organic Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Power Engineering (AREA)
- Materials Engineering (AREA)
- Structural Engineering (AREA)
- Geology (AREA)
- General Life Sciences & Earth Sciences (AREA)
- Environmental & Geological Engineering (AREA)
- Life Sciences & Earth Sciences (AREA)
- Microelectronics & Electronic Packaging (AREA)
- Inorganic Compounds Of Heavy Metals (AREA)
Abstract
Disclosed is a doped anatase titanium dioxide material with the general chemical formula (AxBy)Ti1-3/4x-5/4yO2, wherein A is selected from at least one of Bi, In, Ga and Al, B is selected from at least one of Nb, W, V and Ta, 0<x<0.10, and 0<y<0.10. The sintering temperature of the doped anatase titanium dioxide material mentioned above is relatively low.
Description
本发明涉及一种掺杂锐钛矿二氧化钛材料、其制备方法及其应用。The invention relates to a doped anatase titanium dioxide material, a preparation method thereof and an application thereof.
高能存储器件(比如动态随机存储器)以及超级(普通)电容器的研究表明,组成它们的介电材料应该同时具有高介电常数,低介电损耗以及较宽的温度使用范围。Studies of high-energy memory devices (such as dynamic random access memories) and super (ordinary) capacitors have shown that the dielectric materials that make up them should have both high dielectric constant, low dielectric loss, and a wide temperature range.
目前,双金属离子共掺杂二氧化钛因其独特的介电性能正引起广泛的关注。比如:铟和铌共掺杂二氧化钛陶瓷的介电常数在104以上,介电损耗小于0.05。同时,还能够在很宽的温度范围内(从-180℃到200℃)保持优良的介电性能。其他三价离子和铌共掺杂的二氧化钛陶瓷材料也表现出铟和铌共掺杂二氧化钛陶瓷同样的介电性能。另外,铟和铌共掺杂二氧化钛薄膜在很宽的频率范围内也具有高的介电常数,低的介电损耗。二价钡离子和五价铌离子也一起共掺入二氧化钛陶瓷基体中,他们的介电性能也得到广泛的关注。At present, bimetallic ion co-doped titanium dioxide is attracting widespread attention due to its unique dielectric properties. For example, indium and lanthanum co-doped titania ceramics have a dielectric constant of more than 10 4 and a dielectric loss of less than 0.05. At the same time, excellent dielectric properties can be maintained over a wide temperature range (from -180 ° C to 200 ° C). Other trivalent ions and cerium co-doped titanium dioxide ceramic materials also exhibit the same dielectric properties of indium and lanthanum co-doped titanium dioxide ceramics. In addition, indium and lanthanum co-doped titanium dioxide films also have high dielectric constant and low dielectric loss over a wide frequency range. Divalent europium ions and pentavalent europium ions are also co-doped into the titanium dioxide ceramic matrix, and their dielectric properties have also received extensive attention.
然而,目前常用的掺杂二氧化钛介电材料的烧结温度普遍在1400℃左右,烧结温度较高。However, the sintering temperature of the commonly used doped titanium dioxide dielectric material is generally around 1400 ° C, and the sintering temperature is high.
发明内容:Summary of the invention:
基于此,有必要提供一种烧结温度较低的掺杂锐钛矿二氧化钛材料、其制备方法、由该掺杂锐钛矿二氧化钛材料制成的陶瓷及掺杂锐钛矿二氧化钛材料在陶瓷电容器中的应用。Based on this, it is necessary to provide a doped anatase titanium dioxide material having a lower sintering temperature, a preparation method thereof, a ceramic made of the doped anatase titanium dioxide material, and a doped anatase titanium dioxide material in a ceramic capacitor. Applications.
一种掺杂锐钛矿二氧化钛材料,所述掺杂锐钛矿二氧化钛材料的化学通
式为(AxBy)Ti1-3/4x-5/4yO2,其中,A选自Bi、In、Ga及Al中的至少一种,B选自Nb、W、V及Ta中的至少一种,0<x<0.10,0<y<0.10。One doping anatase titanium dioxide material, through the chemical formula of the doped anatase titanium dioxide material is (A x B y) Ti 1-3 / 4x-5 / 4y O 2, wherein, A is selected from Bi, At least one of In, Ga, and Al, and B is at least one selected from the group consisting of Nb, W, V, and Ta, and 0<x<0.10, 0<y<0.10.
掺杂锐钛矿二氧化钛材料的制备方法,包括以下步骤:The preparation method of the doped anatase titanium dioxide material comprises the following steps:
将含有四价钛的钛源与反应溶剂混合形成预混液,所述预混液中Ti4+的浓度为0.0005mol/L~Ti4+的溶解达到饱和;Mixing a titanium source containing tetravalent titanium with a reaction solvent to form a premixed liquid, wherein the concentration of Ti 4+ in the premixed solution is 0.0005 mol/L to Ti 4+ and the dissolution is saturated;
将含有三价A的A源及含有五价B的B源加入预混液中搅拌至所述A源及所述B源完全溶解形成反应溶液,所述反应溶液中,A3+与Ti4+的摩尔比为n,B5+与Ti4+的摩尔比为m,其中0<n≤2,0<m≤2;所述反应溶液在50℃~250℃下充分反应后得到所述掺杂锐钛矿二氧化钛材料。The A source containing trivalent A and the B source containing pentavalent B are added to the premix and stirred until the source A and the source B are completely dissolved to form a reaction solution in which A 3+ and Ti 4+ are present. The molar ratio is n, the molar ratio of B 5+ to Ti 4+ is m, wherein 0 < n ≤ 2, 0 < m ≤ 2; the reaction solution is fully reacted at 50 ° C to 250 ° C to obtain the blend Miscellaneous anatase titanium dioxide material.
上述掺杂锐钛矿二氧化钛材料,通过共掺杂+3价和+5价金属离子进行化学修饰锐钛矿二氧化钛,经修饰的掺杂锐钛矿二氧化钛材料具有巨介电性能,可以直接用于制备高介电单层或多层陶瓷电容器,用该掺杂锐钛矿二氧化钛材料作为原料直接烧结相应陶瓷,煅烧温度只需要1000℃左右,烧结温度较低。The above doped anatase titanium dioxide material is chemically modified with anatase titanium dioxide by co-doping + trivalent and +5 valent metal ions, and the modified doped anatase titanium dioxide material has a giant dielectric property and can be directly used for A high dielectric single-layer or multi-layer ceramic capacitor is prepared, and the doped anatase titanium dioxide material is used as a raw material to directly sinter the corresponding ceramic, and the calcination temperature only needs about 1000 ° C, and the sintering temperature is low.
图1为实施例1~3制备的掺杂锐钛矿二氧化钛材料的XRD谱图;1 is an XRD spectrum of the doped anatase titanium dioxide material prepared in Examples 1 to 3;
图2为实施例1~3制备的掺杂锐钛矿二氧化钛材料在室温下的拉曼光谱谱图;2 is a Raman spectrum of the doped anatase titanium dioxide material prepared in Examples 1 to 3 at room temperature;
图3为实施例1制备的掺杂锐钛矿二氧化钛材料的透射电镜照片;3 is a transmission electron micrograph of the doped anatase titanium dioxide material prepared in Example 1;
图4为实施例1制备的掺杂锐钛矿二氧化钛材料的XPS图;4 is an XPS diagram of the doped anatase titanium dioxide material prepared in Example 1;
图5为实施例1制备的掺杂锐钛矿二氧化钛材料制成的陶瓷的室温介电频谱图。5 is a room temperature dielectric spectrum diagram of a ceramic made of the doped anatase titanium dioxide material prepared in Example 1.
下面主要结合附图及具体实施例对掺杂锐钛矿二氧化钛材料、其制备方
法、由该掺杂锐钛矿二氧化钛材料制成的陶瓷及掺杂锐钛矿二氧化钛材料在陶瓷电容器中的应用作进一步详细的说明。The following mainly relates to the doped anatase titanium dioxide material with reference to the accompanying drawings and specific examples, and the preparation thereof
The method, the ceramic made of the doped anatase titanium dioxide material and the doped anatase titanium dioxide material are further described in detail in the ceramic capacitor.
一实施方式的掺杂锐钛矿二氧化钛材料的化学通式为(AxBy)Ti1-3/4x-5/4yO2,其中,A选自Bi、In、Ga及Al中的至少一种,B选自Nb、W、V及Ta中的至少一种,0<x<0.10,0<y<0.10。The chemical formula of the doped anatase titanium dioxide material of one embodiment is (A x B y )Ti 1-3/4x-5/4y O 2 , wherein A is at least selected from the group consisting of Bi, In, Ga, and Al. In one case, B is at least one selected from the group consisting of Nb, W, V, and Ta, and 0<x<0.10, 0<y<0.10.
优选的,掺杂锐钛矿二氧化钛材料在一维方向上的尺寸小于100nm。Preferably, the doped anatase titanium dioxide material has a dimension in the one-dimensional direction of less than 100 nm.
优选的,掺杂锐钛矿二氧化钛材料中含有因B5+离子掺杂而诱导的Ti3+离子。Preferably, the doped anatase titanium dioxide material contains Ti 3+ ions induced by B 5+ ion doping.
优选的,由掺杂锐钛矿二氧化钛材料制备的陶瓷的介电损耗小于0.15。Preferably, the ceramic prepared from the doped anatase titanium dioxide material has a dielectric loss of less than 0.15.
优选的,由掺杂锐钛矿二氧化钛材料制备的陶瓷在20Hz到105Hz范围内的介电常数为8000-150000。Preferably, the ceramic prepared from the doped anatase titanium dioxide material has a dielectric constant in the range of 20 Hz to 10 5 Hz of 8,000 to 150,000.
上述掺杂锐钛矿二氧化钛材料,通过共掺杂+3价和+5价金属离子进行化学修饰锐钛矿二氧化钛,经修饰的掺杂锐钛矿二氧化钛材料具有巨介电性能,可以直接用于制备高介电单层或多层陶瓷电容器,用该掺杂锐钛矿二氧化钛材料作为原料直接烧结相应陶瓷,煅烧温度只需要1000℃左右,烧结温度较低;掺杂锐钛矿二氧化钛材料的尺寸较小,作为陶瓷电容器的原材料,可以实现电子器件的微型化以及其生产工艺的可集成性,可以降低成型过程中的煅烧温度,可以降低每层介电薄膜的厚度,提高陶瓷器件的能量密度,这种小的纳米材料可以促进高电容、优良温度稳定性的多层陶瓷电容器的微型化发展。The above doped anatase titanium dioxide material is chemically modified with anatase titanium dioxide by co-doping + trivalent and +5 valent metal ions, and the modified doped anatase titanium dioxide material has a giant dielectric property and can be directly used for A high dielectric single-layer or multi-layer ceramic capacitor is prepared, and the doped anatase titanium dioxide material is used as a raw material to directly sinter the corresponding ceramic, the calcination temperature only needs about 1000 ° C, and the sintering temperature is low; the size of the doped anatase titanium dioxide material Smaller, as a raw material of ceramic capacitors, it can realize the miniaturization of electronic devices and the integration of its production process, which can reduce the calcination temperature in the molding process, reduce the thickness of each dielectric film, and increase the energy density of ceramic devices. This small nanomaterial can promote the miniaturization of multilayer ceramic capacitors with high capacitance and excellent temperature stability.
上述掺杂锐钛矿二氧化钛材料的制备方法,包括以下步骤:The preparation method of the above doped anatase titanium dioxide material comprises the following steps:
步骤S110、将含有四价钛的钛源与反应溶剂混合形成预混液,预混液中Ti4+的浓度为0.0005mol/L至Ti4+的浓度达到饱和。Step S110, mixing a titanium source containing tetravalent titanium with a reaction solvent to form a premixed solution, wherein the concentration of Ti 4+ in the premixed solution is 0.0005 mol/L to a concentration of Ti 4+ saturated.
Ti4+的浓度达到饱和是指钛源在反应溶剂中达到饱和溶解度。Saturating the concentration of Ti 4+ means that the titanium source reaches saturation solubility in the reaction solvent.
优选的,钛源选自Ti(NO3)4、Ti(NO3)4的水合物、TiCl4、TiCl4的水合物、Ti(SO4)2、Ti(SO4)2的水合物、TiOSO4、TiOSO4的水合物、C8H20O4Ti、C8H20O4Ti的水合物、C12H28O4Ti、C12H28O4Ti的水合物、C16H36O4Ti及C16H36O4Ti的水
合物中的至少一种。Preferably, the titanium source is selected from the group consisting of Ti(NO 3 ) 4 , a hydrate of Ti(NO 3 ) 4 , a hydrate of TiCl 4 , TiCl 4 , a hydrate of Ti(SO 4 ) 2 , Ti(SO 4 ) 2 , Hydrate of TiOSO 4 , TiOSO 4 , hydrate of C 8 H 20 O 4 Ti, C 8 H 20 O 4 Ti, hydrate of C 12 H 28 O 4 Ti, C 12 H 28 O 4 Ti, C 16 H At least one of a hydrate of 36 O 4 Ti and C 16 H 36 O 4 Ti.
优选的,反应溶剂选自水、乙醇、甲醇、异丙醇、丙酮以及油酸中的至少一种。Preferably, the reaction solvent is at least one selected from the group consisting of water, ethanol, methanol, isopropanol, acetone, and oleic acid.
优选的,反应溶剂的体积大于5毫升。Preferably, the volume of the reaction solvent is greater than 5 ml.
步骤S120、将含有三价A的A源及含有五价B的B源加入预混液中搅拌至A源及B源完全溶解形成反应溶液。In step S120, the A source containing trivalent A and the B source containing pentavalent B are added to the premixed solution and stirred until the source A and the source B are completely dissolved to form a reaction solution.
其中,反应溶液中,A3+与Ti4+的摩尔比为n,B5+与Ti4+的摩尔比为m,其中0<n≤2,0<m≤2。该步骤中,含有三价A的A源及含有五价B的B源的量根据A3+及B5+在反应溶液中的预设浓度来确定。Wherein, in the reaction solution, the molar ratio of A 3+ to Ti 4+ is n, and the molar ratio of B 5+ to Ti 4+ is m, wherein 0 < n ≤ 2, 0 < m ≤ 2. In this step, the amount of the A source containing trivalent A and the B source containing pentavalent B is determined according to the preset concentration of A 3+ and B 5+ in the reaction solution.
优选的,A源选自A(NO3)3、A(NO3)3的水合物、ACl3、ACl3的水合物、A2(SO4)3、A2(SO4)3的水合物、A(C2H3O2)3及A(C2H3O2)3的水合物中的至少一种。Preferably, the source of A is selected from the group consisting of hydrates of A(NO 3 ) 3 , A(NO 3 ) 3 , hydrates of ACl 3 , ACl 3 , hydration of A 2 (SO 4 ) 3 , A 2 (SO 4 ) 3 At least one of a hydrate of A(C 2 H 3 O 2 ) 3 and A(C 2 H 3 O 2 ) 3 .
优选的,B源选自B(NO3)5、B(NO3)5的水合物、B2(SO4)5、B2(SO4)5的水合物、BCl5及BCl5的水合物中的至少一种。Preferably, the B source is selected from the group consisting of hydrates of B(NO 3 ) 5 , B(NO 3 ) 5 , hydrates of B 2 (SO 4 ) 5 , B 2 (SO 4 ) 5 , hydrate of BCl 5 and BCl 5 . At least one of the substances.
优选的,搅拌在常温下进行。Preferably, the stirring is carried out at normal temperature.
优选的,搅拌的时间为0小时~10小时,优选为1.5小时。Preferably, the stirring time is from 0 hours to 10 hours, preferably 1.5 hours.
步骤S130、使反应溶液在50℃~250℃下充分反应得到掺杂锐钛矿二氧化钛材料。Step S130, the reaction solution is sufficiently reacted at 50 ° C to 250 ° C to obtain a doped anatase titanium dioxide material.
优选的,反应时间为4小时以上。Preferably, the reaction time is 4 hours or more.
优选的,使反应溶液在50℃~250℃下充分反应后分离提纯得到掺杂锐钛矿二氧化钛材料,分离提纯的操作具体为:用水和乙醇依次分别清洗得到的反应产物并离心分离。Preferably, the reaction solution is sufficiently reacted at 50 ° C to 250 ° C to be separated and purified to obtain a doped anatase titanium dioxide material. The separation and purification operation is specifically: separately washing the obtained reaction product with water and ethanol and centrifuging.
优选的,将所述反应溶液收容于密封的反应釜中,将反应釜置于50℃~250℃的加热设备中进行加热,进一步优选的,加热设备为烘箱,水浴,油浴中的至少一种。Preferably, the reaction solution is contained in a sealed reaction vessel, and the reaction vessel is heated in a heating apparatus at 50 ° C to 250 ° C. Further preferably, the heating device is at least one of an oven, a water bath, and an oil bath. Kind.
上述掺杂锐钛矿二氧化钛材料的合成工艺简单,反应条件温和;反应的原料及产物无毒,较为环保;制备的掺杂锐钛矿二氧化钛材料具有较小的颗
粒尺寸;通过改变A3+和B5+离子在反应溶剂中的浓度,可以调控其在掺杂锐钛矿二氧化钛材料中的共掺杂浓度。Synthesis-doped anatase titanium dioxide material is simple, mild reaction conditions; non-toxic raw materials and reaction by-products, more environmentally friendly; doped anatase titanium dioxide material prepared has a smaller particle size; and by changing the A 3+ The concentration of B 5+ ions in the reaction solvent can be adjusted to the co-doping concentration in the doped anatase titanium dioxide material.
一实施方式的陶瓷通过将上述掺杂锐钛矿二氧化钛材料烧结而成。The ceramic of one embodiment is formed by sintering the above-doped anatase titanium dioxide material.
优选的,烧结温度低于1200℃。进一步优选的,烧结的温度为1000℃~1200℃。Preferably, the sintering temperature is below 1200 °C. More preferably, the sintering temperature is from 1000 ° C to 1200 ° C.
优选的,将掺杂锐钛矿二氧化钛材料压制成生坯,再对所述生坯进行烧结。Preferably, the doped anatase titanium dioxide material is pressed into a green body and the green body is sintered.
优选的,烧结在高温炉中进行,Preferably, the sintering is carried out in a high temperature furnace,
优选的,烧结的时间为0.5小时~60小时。Preferably, the sintering time is from 0.5 hours to 60 hours.
上述陶瓷具有高的介电性能,且烧结温度较低。The above ceramics have high dielectric properties and a low sintering temperature.
上述掺杂锐钛矿二氧化钛材料在陶瓷电容器、生物传感器、染料敏化电池、有机-无机杂化材料领域中均可以应用。The above doped anatase titanium dioxide material can be applied in the fields of ceramic capacitors, biosensors, dye-sensitized cells, and organic-inorganic hybrid materials.
掺杂锐钛矿二氧化钛材料颗粒直接作为单层或多层陶瓷电容器的原材料还可以有效地提高单位厚度内的叠层数量,从而提高电容器器件的存储密度。The doped anatase titanium dioxide material particles directly as a raw material of a single-layer or multi-layer ceramic capacitor can also effectively increase the number of laminations per unit thickness, thereby increasing the storage density of the capacitor device.
以下结合具体实施例进行详细说明。The details are described below in conjunction with specific embodiments.
实施例1Example 1
实施例1的掺杂锐钛矿二氧化钛材料的结构通式为:(AxBy)Ti1-3/4x-5/4yO2,其中x=y=0.05,A=In,B=Nb,制备过程如下:The structure of the doped anatase titanium dioxide material of Example 1 is: (A x B y )Ti 1-3/4x-5/4y O 2 , where x=y=0.05, A=In, B=Nb The preparation process is as follows:
(1)将0.68毫升的四氯化钛加入120毫升乙醇溶液中形成溶液A;(1) 0.68 ml of titanium tetrachloride is added to 120 ml of ethanol solution to form a solution A;
(2)将0.092克五氯化铌和1.64克的醋酸铟加入溶液A中形成溶液B;(2) adding 0.092 grams of antimony pentachloride and 1.64 grams of indium acetate to solution A to form a solution B;
(3)溶液B常温下搅拌1.5小时;(3) Solution B is stirred at room temperature for 1.5 hours;
(4)搅拌后的溶液B转入反应釜中并密封反应釜;(4) The stirred solution B is transferred to the reaction vessel and the reaction kettle is sealed;
(5)将反应釜放入200℃的烘箱中反应15小时;(5) The reaction kettle was placed in an oven at 200 ° C for 15 hours;
(6)冷却反应釜后用水和乙醇清洗反应产物,离心之后得到所需的纳米材料。
(6) After cooling the reaction vessel, the reaction product was washed with water and ethanol, and after centrifugation, the desired nanomaterial was obtained.
实施例2Example 2
实施例2的掺杂锐钛矿二氧化钛材料的结构通式为:(AxBy)Ti1-3/4x-5/4yO2,其中x=y=0.03,A=In,B=Nb,制备过程如下:The structure of the doped anatase titanium dioxide material of Example 2 is: (A x B y )Ti 1-3/4x-5/4y O 2 , where x=y=0.03, A=In, B=Nb The preparation process is as follows:
(1)将0.68毫升的四氯化钛加入120毫升乙醇溶液中形成溶液A;(1) 0.68 ml of titanium tetrachloride is added to 120 ml of ethanol solution to form a solution A;
(2)将0.053克五氯化铌和0.8553克的醋酸铟加入溶液A中形成溶液B;(2) adding 0.053 g of antimony pentachloride and 0.8553 g of indium acetate to solution A to form a solution B;
(3)溶液B常温下搅拌1.5小时;(3) Solution B is stirred at room temperature for 1.5 hours;
(4)搅拌后的溶液B转入反应釜中并密封反应釜;(4) The stirred solution B is transferred to the reaction vessel and the reaction kettle is sealed;
(5)将反应釜放入200℃的烘箱中反应15小时;(5) The reaction kettle was placed in an oven at 200 ° C for 15 hours;
(6)冷却反应釜后用水和乙醇清洗反应产物,离心之后得到所需的纳米材料。(6) After cooling the reaction vessel, the reaction product was washed with water and ethanol, and after centrifugation, the desired nanomaterial was obtained.
实施例3Example 3
实施例3的掺杂锐钛矿二氧化钛材料的结构通式为:(AxBy)Ti1-3/4x-5/4yO2,其中x=y=0.01,A=In,B=Nb,制备过程如下:The structure of the doped anatase titanium dioxide material of Example 3 is: (A x B y )Ti 1-3/4x-5/4y O 2 , where x=y=0.01, A=In, B=Nb The preparation process is as follows:
(1)将0.68毫升的四氯化钛加入120毫升乙醇溶液中形成溶液A;(1) 0.68 ml of titanium tetrachloride is added to 120 ml of ethanol solution to form a solution A;
(2)将0.0388克五氯化铌和0.446克的醋酸铟加入溶液A中形成溶液B;(2) adding 0.0388 g of antimony pentachloride and 0.446 g of indium acetate to solution A to form solution B;
(3)溶液B常温下搅拌1.5小时;(3) Solution B is stirred at room temperature for 1.5 hours;
(4)搅拌后的溶液B转入反应釜中并密封反应釜;(4) The stirred solution B is transferred to the reaction vessel and the reaction kettle is sealed;
(5)将反应釜放入200℃的烘箱中反应15小时;(5) The reaction kettle was placed in an oven at 200 ° C for 15 hours;
(6)冷却反应釜后用水和乙醇清洗反应产物,离心之后得到所需的纳米材料。(6) After cooling the reaction vessel, the reaction product was washed with water and ethanol, and after centrifugation, the desired nanomaterial was obtained.
请参阅图1,图1为实施例1(5at.%In3+和5at.%Nb5+)、实施例2(3at.%In3+和3at.%Nb5+)及实施例3(1at.%In3+和1at.%Nb5+)制备的掺杂锐钛矿二氧化钛材料的XRD谱图。从图1中可以看出合成的铟和铌离子共掺杂二氧化钛纳米材料具有锐钛矿晶体结构,也说明实施例1~3制备的掺杂锐钛矿二氧化钛材料具有单相特征而不含有其他杂质。Please refer to FIG. 1. FIG. 1 is an embodiment 1 (5 at.% In 3+ and 5 at.% Nb 5+ ), Example 2 (3 at.% In 3+ and 3 at.% Nb 5+ ), and Example 3 ( XRD patterns of doped anatase titanium dioxide materials prepared by 1 at. % In 3 + and 1 at. % Nb 5+ ). It can be seen from Fig. 1 that the synthesized indium and cerium ion co-doped TiO 2 nanomaterials have an anatase crystal structure, and also demonstrate that the doped anatase titanium dioxide materials prepared in Examples 1-3 have a single phase characteristic and do not contain other Impurities.
请参阅图2,图2为实施例1(5at.%In3+和5at.%Nb5+)、实施例2(3at.%
In3+和3at.%Nb5+)及实施例3(1at.%In3+和1at.%Nb5+)制备的掺杂锐钛矿二氧化钛材料在室温下的拉曼光谱谱图。从图2中可以看出合成的铟和铌离子共掺杂二氧化钛纳米材料具有锐钛矿晶体结构。Please refer to FIG. 2. FIG. 2 is Embodiment 1 (5 at.% In 3+ and 5 at.% Nb 5+ ), Example 2 (3 at.% In 3+ and 3 at.% Nb 5+ ), and Example 3 ( Raman spectra of doped anatase titanium dioxide material prepared at 1 at.%In 3+ and 1 at.% Nb 5+ ) at room temperature. It can be seen from Fig. 2 that the synthesized indium and cerium ion co-doped TiO 2 nanomaterials have an anatase crystal structure.
请参阅图3,图3为实施例1制备的掺杂锐钛矿二氧化钛材料的透射电镜照片。从图3可以看出合成的铟和铌离子共掺杂二氧化钛纳米材料的粒径为10nm左右。Please refer to FIG. 3. FIG. 3 is a transmission electron micrograph of the doped anatase titanium dioxide material prepared in Example 1. It can be seen from Fig. 3 that the synthesized indium and cerium ion co-doped TiO 2 nanomaterials have a particle size of about 10 nm.
请参阅图4,图4为实施例1制备的掺杂锐钛矿二氧化钛材料的XPS图。从图4可以看出合成的铟和铌离子共掺杂二氧化钛纳米材料中含有Ti3+离子。Please refer to FIG. 4. FIG. 4 is an XPS diagram of the doped anatase titanium dioxide material prepared in Example 1. It can be seen from Fig. 4 that the synthesized indium and cerium ion co-doped titanium dioxide nanomaterials contain Ti 3+ ions.
将实施例1制备的掺杂锐钛矿二氧化钛材料压制成直径为1.1cm的圆柱体生坯,将生坯在1200℃烧结20小时后得到陶瓷。请参阅图5,图5为实施例1制备的掺杂锐钛矿二氧化钛材料制成的陶瓷的室温介电频谱图。该室温介电频谱说明利用该纳米粉制备的陶瓷在20Hz到105Hz范围内具有高的介电常数(8000-150000),介电损耗小于0.15。The doped anatase titanium dioxide material prepared in Example 1 was pressed into a cylindrical green body having a diameter of 1.1 cm, and the green body was sintered at 1200 ° C for 20 hours to obtain a ceramic. Please refer to FIG. 5. FIG. 5 is a room temperature dielectric spectrum diagram of a ceramic made of the doped anatase titanium dioxide material prepared in Example 1. The room temperature dielectric spectrum indicates that the ceramic prepared using the nanopowder has a high dielectric constant (8000-150000) in the range of 20 Hz to 10 5 Hz and a dielectric loss of less than 0.15.
请参阅表1,表1为实施例1~3制备的掺杂锐钛矿二氧化钛材料的能谱(EDS)表,EDS结果由扫描电镜直接测试得到。Please refer to Table 1. Table 1 shows the energy spectrum (EDS) of the doped anatase titanium dioxide materials prepared in Examples 1 to 3. The EDS results were directly tested by scanning electron microscopy.
表1Table 1
样品sample | Ti(at.%)Ti(at.%) | Nb(at.%)Nb (at.%) | In(at.%)In(at.%) | Nb∶TiNb:Ti | In∶TiIn:Ti |
实施例1Example 1 | 32.6632.66 | 0.330.33 | 0.350.35 | 1.01∶1001.01:100 | 1.07∶1001.07:100 |
实施例2Example 2 | 31.4331.43 | 1.001.00 | 0.890.89 | 3.19∶1003.19:100 | 2.81∶1002.81:100 |
实施例3Example 3 | 30.2530.25 | 1.541.54 | 1.551.55 | 5.09∶1005.09:100 | 5.11∶1005.11:100 |
从表1可以看出实施例1~3制备的掺杂锐钛矿二氧化钛材料中确实存在銦和铌掺杂离子,并且掺杂离子的浓度可以在样品中进行调控。It can be seen from Table 1 that indium and antimony doped ions are indeed present in the doped anatase titanium dioxide material prepared in Examples 1 to 3, and the concentration of the doping ions can be regulated in the sample.
以上所述实施例仅表达了本发明的一种或几种实施方式,其描述较为具体和详细,但并不能因此而理解为对本发明专利范围的限制。应当指出的是,对于本领域的普通技术人员来说,在不脱离本发明构思的前提下,还可以做出若干变形和改进,这些都属于本发明的保护范围。因此,本发明专利的保
护范围应以所附权利要求为准。
The above-mentioned embodiments are merely illustrative of one or more embodiments of the present invention, and the description thereof is not to be construed as limiting the scope of the invention. It should be noted that a number of variations and modifications may be made by those skilled in the art without departing from the spirit and scope of the invention. Therefore, the protection of the patent of the present invention
The scope of protection shall be subject to the appended claims.
Claims (19)
- 一种掺杂锐钛矿二氧化钛材料,其特征在于,所述掺杂锐钛矿二氧化钛材料的化学通式为(AxBy)Ti1-3/4x-5/4yO2,其中,A选自Bi、In、Ga及Al中的至少一种,B选自Nb、W、V及Ta中的至少一种,0<x<0.10,0<y<0.10。A doped anatase titanium dioxide material, characterized in that the doped anatase titanium dioxide material has a chemical formula of (A x B y )Ti 1-3/4x-5/4y O 2 , wherein A At least one selected from the group consisting of Bi, In, Ga, and Al, and B is at least one selected from the group consisting of Nb, W, V, and Ta, and 0<x<0.10, 0<y<0.10.
- 根据权利要求1所述的掺杂锐钛矿二氧化钛材料,其特征在于,所述掺杂锐钛矿二氧化钛材料在一维方向上的尺寸小于100nm。The doped anatase titanium dioxide material according to claim 1, wherein the doped anatase titanium dioxide material has a size in a one-dimensional direction of less than 100 nm.
- 根据权利要求1所述的掺杂锐钛矿二氧化钛材料,其特征在于,所述掺杂锐钛矿二氧化钛材料中含有因B5+离子掺杂而诱导的Ti3+离子。The doped anatase titanium dioxide material according to claim 1, wherein the doped anatase titanium dioxide material contains Ti 3+ ions induced by B 5+ ion doping.
- 根据权利要求1所述的掺杂锐钛矿二氧化钛材料,其特征在于,由所述掺杂锐钛矿二氧化钛材料制备的陶瓷的介电损耗小于0.15。The doped anatase titanium dioxide material according to claim 1, wherein the ceramic prepared from the doped anatase titanium dioxide material has a dielectric loss of less than 0.15.
- 根据权利要求1所述的掺杂锐钛矿二氧化钛材料,其特征在于,由所述掺杂锐钛矿二氧化钛材料制备的陶瓷在20Hz到105Hz范围内的介电常数为8000-150000。The doped anatase titanium dioxide material according to claim 1, wherein the ceramic prepared from the doped anatase titanium dioxide material has a dielectric constant in the range of 20 Hz to 10 5 Hz of 8,000 to 150,000.
- 如权利要求1~5任一项的掺杂锐钛矿二氧化钛材料的制备方法,其特征在于,包括以下步骤:The method for preparing a doped anatase titanium dioxide material according to any one of claims 1 to 5, comprising the steps of:将含有四价钛的钛源与反应溶剂混合形成预混液,所述预混液中Ti4+的浓度为0.0005mol/L至Ti4+的溶解达到饱和;Mixing a titanium source containing tetravalent titanium with a reaction solvent to form a premixed liquid, wherein the concentration of Ti 4+ in the premixed solution is 0.0005 mol/L until the dissolution of Ti 4+ reaches saturation;将含有三价A的A源及含有五价B的B源加入预混液中搅拌至所述A源及所述B源完全溶解形成反应溶液,所述反应溶液中,A3+与Ti4+的摩尔比为n,B5+与Ti4+的摩尔比为m,其中0<n≤2,0<m≤2;所述反应溶液在50℃~250℃下充分反应后得到所述掺杂锐钛矿二氧化钛材料。The A source containing trivalent A and the B source containing pentavalent B are added to the premix and stirred until the source A and the source B are completely dissolved to form a reaction solution in which A 3+ and Ti 4+ are present. The molar ratio is n, the molar ratio of B 5+ to Ti 4+ is m, wherein 0 < n ≤ 2, 0 < m ≤ 2; the reaction solution is fully reacted at 50 ° C to 250 ° C to obtain the blend Miscellaneous anatase titanium dioxide material.
- 根据权利要求6所述的掺杂锐钛矿二氧化钛材料的制备方法,其特征在于,所述钛源选自Ti(NO3)4、Ti(NO3)4的水合物、TiCl4、TiCl4的水合物、Ti(SO4)2、Ti(SO4)2的水合物、TiOSO4、TiOSO4的水合物、C8H20O4Ti、C8H20O4Ti的水合物、C12H28O4Ti、C12H28O4Ti的水合物、C16H36O4Ti及C16H36O4Ti的水合物中的至少一种。The method for preparing a doped anatase titanium dioxide material according to claim 6, wherein the titanium source is selected from the group consisting of Ti(NO 3 ) 4 , Ti(NO 3 ) 4 hydrate, TiCl 4 , TiCl 4 . Hydrate, hydrate of Ti(SO 4 ) 2 , Ti(SO 4 ) 2 , hydrate of TiOSO 4 , TiOSO 4 , hydrate of C 8 H 20 O 4 Ti, C 8 H 20 O 4 Ti, C At least one of a hydrate of 12 H 28 O 4 Ti, C 12 H 28 O 4 Ti, a hydrate of C 16 H 36 O 4 Ti and C 16 H 36 O 4 Ti.
- 根据权利要求6所述的掺杂锐钛矿二氧化钛材料的制备方法,其特征 在于,所述反应溶剂选自水、乙醇、甲醇、异丙醇、丙酮以及油酸中的至少一种。The method for preparing an anatase titanium dioxide material according to claim 6, characterized in that The reaction solvent is at least one selected from the group consisting of water, ethanol, methanol, isopropanol, acetone, and oleic acid.
- 根据权利要求6所述的掺杂锐钛矿二氧化钛材料的制备方法,其特征在于,所述A源选自A(NO3)3、A(NO3)3的水合物、ACl3、ACl3的水合物、A2(SO4)3、A2(SO4)3的水合物、A(C2H3O2)3及A(C2H3O2)3的水合物中的至少一种。The method for preparing an anatase titanium dioxide material according to claim 6, wherein the source A is selected from the group consisting of A(NO 3 ) 3 , A(NO 3 ) 3 hydrate, ACl 3 , and ACl 3 . a hydrate, at least one of a hydrate of A 2 (SO 4 ) 3 , A 2 (SO 4 ) 3 , a hydrate of A(C 2 H 3 O 2 ) 3 and A(C 2 H 3 O 2 ) 3 One.
- 根据权利要求6所述的掺杂锐钛矿二氧化钛材料的制备方法,其特征在于,所述B源选自B(NO3)5、B(NO3)5的水合物、B2(SO4)5、B2(SO4)5的水合物、BCl5及BCl5的水合物中的至少一种。The method for preparing anatase titanium dioxide doped material according to claim 6, wherein the source of B is selected from B (NO 3) 5, B (NO 3) hydrate 5, B 2 (SO 4 ) 5, B 2 (SO 4 hydrate) 5, BCl 5, and at least one of BCl hydrates. 5.
- 根据权利要求6所述的掺杂锐钛矿二氧化钛材料的制备方法,其特征在于,所述反应溶液在50℃~250℃下充分反应的步骤中,反应时间为4小时以上。The method for preparing a doped anatase titanium dioxide material according to claim 6, wherein the reaction solution has a reaction time of 4 hours or more in the step of sufficiently reacting at 50 ° C to 250 ° C.
- 根据权利要求6所述的掺杂锐钛矿二氧化钛材料的制备方法,其特征在于,所述反应溶液在50℃~250℃下充分反应后进行分离提纯得到所述掺杂锐钛矿二氧化钛材料,所述分离提纯的操作具体为:用水和乙醇依次清洗得到的反应产物并离心分离。The method for preparing an anatase titanium dioxide material according to claim 6, wherein the reaction solution is sufficiently reacted at 50 ° C to 250 ° C to be separated and purified to obtain the doped anatase titanium dioxide material. The separation and purification operation is specifically: sequentially washing the obtained reaction product with water and ethanol and centrifuging.
- 根据权利要求6所述的掺杂锐钛矿二氧化钛材料的制备方法,其特征在于,所述反应溶液在50℃~250℃下充分反应的步骤中,将所述反应溶液置于密封的反应釜中,将所述反应釜置于50℃~250℃的加热设备中进行加热。The method for preparing a doped anatase titanium dioxide material according to claim 6, wherein in the step of fully reacting the reaction solution at 50 ° C to 250 ° C, the reaction solution is placed in a sealed reaction vessel. The reaction vessel is placed in a heating apparatus at 50 ° C to 250 ° C for heating.
- 根据权利要求13所述的掺杂锐钛矿二氧化钛材料的制备方法,其特征在于,所述加热设备为烘箱,水浴,油浴中的至少一种。The method for preparing an anatase titanium dioxide material according to claim 13, wherein the heating device is at least one of an oven, a water bath, and an oil bath.
- 一种陶瓷,其特征在于,所述陶瓷通过将权利要求1~5任一项的掺杂锐钛矿二氧化钛材料烧结而成。A ceramic characterized in that the ceramic is obtained by sintering the doped anatase titanium dioxide material according to any one of claims 1 to 5.
- 根据权利要求15所述的陶瓷,其特征在于,所述烧结的温度低于1200℃。The ceramic according to claim 15, wherein the sintering temperature is lower than 1200 °C.
- 根据权利要求15所述的陶瓷,其特征在于,将权利要求1~4任一项的掺杂锐钛矿二氧化钛材料烧结时,将所述掺杂锐钛矿二氧化钛材料压制成 生坯,再对所述生坯进行烧结。The ceramic according to claim 15, wherein when the doped anatase titanium dioxide material of any one of claims 1 to 4 is sintered, the doped anatase titanium dioxide material is pressed into The green body is then sintered.
- 根据权利要求15所述的陶瓷,其特征在于,所述烧结的时间为0.5小时~60小时。The ceramic according to claim 15, wherein the sintering time is from 0.5 hours to 60 hours.
- 权利要求1~5任一项的掺杂锐钛矿二氧化钛材料在陶瓷电容器、生物传感器、染料敏化电池、有机-无机杂化材料领域中的应用。 Use of the doped anatase titanium dioxide material according to any one of claims 1 to 5 in the field of ceramic capacitors, biosensors, dye-sensitized cells, and organic-inorganic hybrid materials.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
PCT/CN2016/080924 WO2017190277A1 (en) | 2016-05-03 | 2016-05-03 | Doped anatase titanium dioxide material, preparation method therefor and use thereof |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
PCT/CN2016/080924 WO2017190277A1 (en) | 2016-05-03 | 2016-05-03 | Doped anatase titanium dioxide material, preparation method therefor and use thereof |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2017190277A1 true WO2017190277A1 (en) | 2017-11-09 |
Family
ID=60202660
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/CN2016/080924 WO2017190277A1 (en) | 2016-05-03 | 2016-05-03 | Doped anatase titanium dioxide material, preparation method therefor and use thereof |
Country Status (1)
Country | Link |
---|---|
WO (1) | WO2017190277A1 (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN109534393A (en) * | 2018-12-01 | 2019-03-29 | 韩城市微晶电子材料有限公司 | A kind of preparation method of the octahedrite nano titanium dioxide powder of witch culture |
WO2019129463A1 (en) * | 2017-12-27 | 2019-07-04 | Leibniz-Institut Für Neue Materialien Gemeinnützige Gmbh | Conductive materials made of nb-doped tio2-particles |
CN112678867A (en) * | 2020-12-25 | 2021-04-20 | 苏州锦艺新材料科技有限公司 | Rutile type titanium dioxide and preparation method and application thereof |
CN116283272A (en) * | 2023-02-14 | 2023-06-23 | 哈尔滨理工大学 | Room temperature ferrotitanium oxide ceramic and its preparation method and application |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102471088A (en) * | 2009-07-30 | 2012-05-23 | 国立大学法人东京大学 | Photocatalytic material and preparation method thereof |
CN103958414A (en) * | 2011-09-16 | 2014-07-30 | 澳大利亚国立大学 | Giant dielectric constant material |
CN104169080A (en) * | 2011-09-13 | 2014-11-26 | 法蒂·多甘 | Nanostructured dielectric materials for high energy density multilayer ceramic capacitors |
-
2016
- 2016-05-03 WO PCT/CN2016/080924 patent/WO2017190277A1/en active Application Filing
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102471088A (en) * | 2009-07-30 | 2012-05-23 | 国立大学法人东京大学 | Photocatalytic material and preparation method thereof |
CN104169080A (en) * | 2011-09-13 | 2014-11-26 | 法蒂·多甘 | Nanostructured dielectric materials for high energy density multilayer ceramic capacitors |
CN103958414A (en) * | 2011-09-16 | 2014-07-30 | 澳大利亚国立大学 | Giant dielectric constant material |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2019129463A1 (en) * | 2017-12-27 | 2019-07-04 | Leibniz-Institut Für Neue Materialien Gemeinnützige Gmbh | Conductive materials made of nb-doped tio2-particles |
US11618690B2 (en) | 2017-12-27 | 2023-04-04 | Leibniz-Institut Für Neue Materialien Gemeinnützige Gmbh | Conductive materials made of Nb-doped TiO2 particles |
CN109534393A (en) * | 2018-12-01 | 2019-03-29 | 韩城市微晶电子材料有限公司 | A kind of preparation method of the octahedrite nano titanium dioxide powder of witch culture |
CN112678867A (en) * | 2020-12-25 | 2021-04-20 | 苏州锦艺新材料科技有限公司 | Rutile type titanium dioxide and preparation method and application thereof |
CN112678867B (en) * | 2020-12-25 | 2022-01-14 | 苏州锦艺新材料科技股份有限公司 | Rutile type titanium dioxide and preparation method and application thereof |
CN116283272A (en) * | 2023-02-14 | 2023-06-23 | 哈尔滨理工大学 | Room temperature ferrotitanium oxide ceramic and its preparation method and application |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
Phoon et al. | A review of synthesis and morphology of SrTiO 3 for energy and other applications | |
CN106006726B (en) | Doped anatase titanic oxide material, preparation method and its application | |
Pithan et al. | Progress in the synthesis of nanocrystalline BaTiO3 powders for MLCC | |
WO2017190277A1 (en) | Doped anatase titanium dioxide material, preparation method therefor and use thereof | |
Wang et al. | Direct observation of stable negative capacitance in SrTiO3@ BaTiO3 heterostructure | |
Adak et al. | Ferroelectric and photocatalytic behavior of Mn-and Ce-doped BaTiO3 nanoceramics prepared by chemical route | |
Zeng et al. | Microstructure and dielectric properties of SrTiO3 ceramics by controlled growth of silica shells on SrTiO3 nanoparticles | |
Mohammadi et al. | Sol–gel derived nanocrystalline and mesoporous barium strontium titanate prepared at room temperature | |
Alkathy et al. | Colossal dielectric permittivity and high energy storage efficiency in barium strontium titanate ceramics co-doped with bismuth and lithium | |
Chen et al. | Dielectric properties and impedance analysis of BaTiO3-based ceramics with core-shell structure | |
Zhang et al. | Synthesis of tetragonal BaTiO3 nano-particle via a novel tartaric acid co-precipitation process | |
Wang et al. | Enhancing energy storage density of (Ba, Sr) TiO 3 ceramic particles by coating with Al 2 O 3 and SiO 2 | |
CN107151029A (en) | A kind of sol gel synthesis preparation technology of tetra phase barium titanate powder | |
Qin et al. | Hydrothermal synthesis of perovskite BiFeO3–BaTiO3 crystallites | |
Shih et al. | Manipulation of morphology of strontium titanate particles by spray pyrolysis | |
US20140005029A1 (en) | Method of manufacturing perovskite powder, perovskite powder manufactured by the same and multilayer ceramic electronic component | |
JP2003261329A (en) | Barium titanate superfine particle having high crystallinity and production method therefor | |
Jana et al. | Microstructure and dielectric characteristics of Ni ion doped BaTiO3 nanoparticles | |
Satheesan et al. | Influence of defects on the photocatalytic activity of Niobium-doped ZnO nanoparticles | |
Sasirekha et al. | Hydrothermal synthesis of barium titanate: Effect of titania precursor and calcination temperature on phase transition | |
Ahmed et al. | High Dielectric Constant Study of TiO2‐Polypyrrole Composites with Low Contents of Filler Prepared by In Situ Polymerization | |
Saeed et al. | Structural and dielectric properties of iron doped barium strontium titanate for storage applications | |
JP6149039B2 (en) | Ultrafine titanium dioxide and method for producing the same | |
Lee et al. | Sonochemical activation in aqueous medium for solid-state synthesis of BaTiO3 powders | |
Zhao et al. | Growth mechanism, modified morphology and optical properties of coral-like BaTiO3 architecture through CTAB assisted synthesis |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
NENP | Non-entry into the national phase |
Ref country code: DE |
|
121 | Ep: the epo has been informed by wipo that ep was designated in this application |
Ref document number: 16900799 Country of ref document: EP Kind code of ref document: A1 |
|
122 | Ep: pct application non-entry in european phase |
Ref document number: 16900799 Country of ref document: EP Kind code of ref document: A1 |