CN1792817A - Process for preparing anatase type nano crystal TiO2 solar energy cell material - Google Patents
Process for preparing anatase type nano crystal TiO2 solar energy cell material Download PDFInfo
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- CN1792817A CN1792817A CNA2005101104460A CN200510110446A CN1792817A CN 1792817 A CN1792817 A CN 1792817A CN A2005101104460 A CNA2005101104460 A CN A2005101104460A CN 200510110446 A CN200510110446 A CN 200510110446A CN 1792817 A CN1792817 A CN 1792817A
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Abstract
A process for preparing anatase-type TiO2 nano-crystals used for dye-sensitive solar cell, photocatalyst, photo-cleaning material and gas-sensitive material includes such steps as hydrolyzing titanate to obtain deposit, washing, adding it to the aqueous solution of quaternary ammonium alkali, thermal reflux to obtain sol, and holding 190-230 deg.C in a sealed teflon container.
Description
Technical field
The present invention relates to a kind of nanocrystalline TiO
2The preparation method of solar cell material relates in particular to a kind of anatase type nano crystal TiO that has
2The preparation method of solar cell material.Belong to solar cell material preparation and Application Areas.
Background technology
Society's fast development makes resource and energy dilemma become increasingly conspicuous, and develops the vital task that pollution-free, reproducible new forms of energy become science and technology research.Sun power discharges great amount of carbon dioxide gas and causes " Greenhouse effect ", thereby have broad application prospects as a kind of novel renewable energy source unlike conventional energy resources.At present, solar cell is one of valid approach of development and use sun power.Because the preparation more complicated of inorganic solar cell such as silicon, production cost is high, has limited its widespread use.The Michael Gr tzel of engineering institute such as Lausanne, SUI height in 1991 find to do with transition metal Ru title complex the nanometer crystal film TiO of dyestuff
2Dye sensitization solar battery, its photovoltaic energy conversion efficient reaches 7.1～7.9% (simulated solar irradiations), and the photoelectric transformation efficiency of this battery in 1997 has reached 10～11%, based on TiO
2The research of the dye sensitization solar battery of epitaxial has caused that people pay close attention to greatly.Nowadays, dye sensitization solar battery has worldwide become the research focus.
The effciency of energy transfer of dye sensitization solar battery and TiO
2The character of epitaxial is relevant, and it comprises specific surface area, voidage, the scattering of light performance of epitaxial and the TiO that constitutes the nanometer crystal film material
2Crystal formation, particle diameter etc.Titanium dioxide has three kinds of common crystal formations, i.e. anatase octahedrite, and brookite and rutile, the battery thin film with titanium dioxide nanocrystalline material preparation of Detitanium-ore-type has photoelectric properties preferably.People such as N.G.Park are at " J.Phys.Chem. " B, 2000,104,8989 studies show that the rutile titanic oxide electronic transmission is slower, its existence can influence the electricity conversion of dye sensitization solar battery.
Present dye sensibilization solar cell nanometer TiO
2Material adopts the titanic acid ester hydrolysis usually, under acidic conditions as salpeter solution in collosol and gel and hot-pressing processing be prepared the nano-TiO that this preparation method obtains
2Often impure, contain the TiO of a certain amount of rutile ore and brookite structure
2, and the existence of rutile ore can influence the photoelectric properties of solar cell.
Summary of the invention
The objective of the invention is at the deficiencies in the prior art, a kind of preparation anatase type nano crystal TiO is provided
2The method of solar cell material is avoided red schorl type nanocrystalline TiO in the solar cell material
2Generation, to improve the photoelectric properties of solar cell.
For realizing this purpose, the present invention at first obtains throw out with titanic acid ester through hydrolysis, then throw out is cleaned and changed in organic quaternary ammonium hydroxide aqueous solution, reflux is carried out colloidal sol, after colloidal sol is finished, in 190～230 ℃ teflon seal container, be incubated, can obtain the nanocrystalline battery material of anatase titanium dioxide.Also can further adopt TiO afterwards
2Nanocrystalline noble metal loading or anion doped or cation doping technology are carried out modification and are handled, and obtain the nanocrystalline battery material of anatase titania of modified.
The present invention prepares anatase type nano crystal TiO
2The method of solar cell material is specially:
At first the titanic acid ester hydrolysis in 0～20 ℃ of scope with certain volume obtains white depositions, throw out is cleaned, and transfer in organic quaternary ammonium hydroxide aqueous solution, wherein the concentration of organic quaternary ammonium hydroxide is by mol ratio 15～750: 1 control of titanic acid ester and organic quaternary ammonium hydroxide, then in 100～120 ℃ of scope stirring and refluxing, carry out colloidal sol, after colloidal sol is finished, colloidal sol is transferred to the pressure pan of inner liner polytetrafluoroethylene, 190 ℃～230 ℃ insulations 4～24 hours, cooling back centrifugation lixiviating obtains the anatase type nano crystal TiO of particle diameter between 8～30nm after the drying
2Solar cell material.
Titanic acid ester of the present invention is for having Ti (OR)
4The compound of forming constitutional features is as isopropyl titanate, tetrabutyl titanate etc.
Organic quaternary ammonium hydroxide of the present invention is formed the compound of constitutional features for having tetra-alkyl ammonium hydroxide, as Tetramethylammonium hydroxide, tetraethyl ammonium hydroxide, TPAOH, TBAH etc.
Titanium dioxide nanocrystalline particle diameter of the present invention can recently be controlled its size by the mole of regulating titanic acid ester and organic quaternary ammonium hydroxide.
Anatase type nano crystal TiO of the present invention
2Solar cell material also can pass through at above-mentioned preparation anatase type nano crystal TiO
2In the process or the preparation finish after, via existing known nanocrystalline TiO
2Modification technique carries out modification to it and obtains, and these modification techniques can be TiO
2Nanocrystalline noble metal loading or anion doped or cation doping technology etc.
The anatase type nano crystal TiO that the inventive method makes
2Solar cell material still can keep pure anatase crystal being heated under 650 ℃ the situation.
Method provided by the invention is used to prepare the nanocrystalline TiO of anatase crystal
2Solar cell material, and the nanocrystalline TiO of preparation
2Grain-size is controlled, does not contain rutile TiO
2, not only may be used in the dye sensitization solar battery, but also may be used on aspects such as organic photochemical catalysis, light automatically cleaning and gas sensitive material.
Description of drawings
Fig. 1 is with the X ray diffracting spectrum of the resulting titanium dioxide nanocrystalline of preparation method provided by the invention behind 650 ℃ of sintering.
Fig. 2 is the X ray diffracting spectrum of the titanium dioxide nanocrystalline that directly obtains with preparation method provided by the invention.
Fig. 3 is correlated with preparation method of the present invention, the titanium dioxide nanocrystalline X ray diffracting spectrum that collosol and gel and hot-pressing processing obtain in the 0.1M salpeter solution.
Embodiment
Below in conjunction with drawings and Examples technical scheme of the present invention is further described.Following examples do not constitute limitation of the invention.
Embodiment 1:
Different third titanic acid ester is dropwise joined in frozen water is cooled to 0 ℃ deionized water, obtain white precipitate.Behind the separating, washing precipitation is transferred in the tetramethyl ammonium hydroxide solution, wherein the concentration of tetramethyl ammonium hydroxide is control in 62.5: 1 by the mol ratio of different third titanic acid ester and tetramethyl ammonium hydroxide, and under agitation 100 ℃ of backflows are to obtain colloidal solution.Above-mentioned colloid is transferred to the pressure pan of inner liner polytetrafluoroethylene, in 210 ℃ of insulations 12 hours, the centrifugation lixiviating, obtaining particle diameter after the drying is that the 14nm anatase titanium dioxide is nanocrystalline.
Embodiment 2:
Tetrabutyl titanate dropwise joined in 20 ℃ the deionized water, obtain white precipitate.Behind the separating, washing precipitation is transferred in the solution of tetraethyl ammonium hydroxide, wherein the concentration of tetraethyl ammonium hydroxide is control in 62.5: 4 by the mol ratio of tetrabutyl titanate and tetramethyl ammonium hydroxide, and under agitation 120 ℃ of backflows are to obtain colloidal solution.Above-mentioned colloid is transferred to the pressure pan of inner liner polytetrafluoroethylene, in 230 ℃ of insulations 24 hours, the centrifugation lixiviating, obtaining particle diameter after the drying is that the 30nm anatase titania is nanocrystalline.
Embodiment 3:
Different third titanic acid ester dropwise joined in 15 ℃ the deionized water, obtain white precipitate.Behind the separating, washing precipitation is transferred in the solution of tetramethyl ammonium hydroxide, wherein the concentration of tetramethyl ammonium hydroxide is control in 750: 1 by the mol ratio of different third titanic acid ester and tetramethyl ammonium hydroxide, and under agitation 100 ℃ of backflows are to obtain colloidal solution.Above-mentioned colloid is transferred to the pressure pan of inner liner polytetrafluoroethylene, in 190 ℃ of insulations 4 hours, the centrifugation lixiviating, obtaining particle diameter after the drying is that the 8nm anatase titania is nanocrystalline.
Embodiment 4:
The particle diameter that embodiment 1 is made is that the pure anatase titania of 14nm is nanocrystalline, is soaked in the Yb that contains 0.1mol/L
3+The aqueous solution 1 hour, take out dry after 450 ℃ of sintering 30 minutes, cooling can obtain through the anatase titania of cation doping nanocrystalline.
Fig. 1 is with the X ray diffracting spectrum of the resulting titanium dioxide nanocrystalline of preparation method provided by the invention behind 650 ℃ of sintering.Collection of illustrative plates shows that the titanium dioxide crystal form that the comparatively high temps sintering obtains still is Detitanium-ore-type.
Fig. 2 is the X ray diffracting spectrum of the titanium dioxide nanocrystalline that directly obtains with preparation method provided by the invention.Warp and standard spectrogram compare, and obtaining titanium dioxide is anatase crystal.
Fig. 3 has provided with preparation method of the present invention correlated, the titanium dioxide nanocrystalline X ray diffracting spectrum that collosol and gel and hot-pressing processing obtain in the 0.1M salpeter solution, among the figure in 2 θ=25.7 ° and 27.5 ° of positions diffraction peak of having occurred brookite and rutile crystal type respectively occur, the nano titanium oxide that shows this preparation method's preparation had both contained anatase crystal and had also contained brookite and rutile crystal type.
Claims (4)
1, a kind of anatase type nano crystal TiO
2The preparation method of solar cell material, it is characterized in that at first titanic acid ester 0～20 ℃ of scope hydrolysis, the throw out that obtains is cleaned, and transfer in organic quaternary ammonium hydroxide aqueous solution, wherein the concentration of organic quaternary ammonium hydroxide is by mol ratio 15～750: 1 control of titanic acid ester and organic quaternary ammonium hydroxide, then in 100～120 ℃ of scope stirring and refluxing, carry out colloidal sol, again colloidal sol is transferred to the pressure pan of inner liner polytetrafluoroethylene, 190 ℃～230 ℃ insulations 4～24 hours, cooling back centrifugation lixiviating obtains the anatase type nano crystal TiO of particle diameter between 8～30nm after the drying
2Solar cell material.
2, according to the anatase type nano crystal TiO of claim 1
2The preparation method of solar cell material is characterized in that described titanic acid ester has Ti (OR)
4Form constitutional features, comprise isopropyl titanate, tetrabutyl titanate.
3, according to the anatase type nano crystal TiO of claim 1
2The preparation method of solar cell material is characterized in that described organic quaternary ammonium hydroxide has tetra-alkyl ammonium hydroxide and forms constitutional features, comprises Tetramethylammonium hydroxide, tetraethyl ammonium hydroxide, TPAOH, TBAH.
4, according to the anatase type nano crystal TiO of claim 1
2The preparation method of solar cell material is characterized in that preparing material after finishing again through TiO
2Nanocrystalline noble metal loading or anion doped or cation doping Technique on T iO
2Carry out modification, obtain the anatase type nano crystal TiO of modified
2Solar cell material.
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Cited By (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN100583463C (en) * | 2007-11-28 | 2010-01-20 | 中国科学院上海硅酸盐研究所 | Production method for titanium oxide coating material in dye sensitized solar battery |
| CN101982417A (en) * | 2010-09-27 | 2011-03-02 | 彩虹集团公司 | Preparation method of titanium dioxide nanocrystalline sol |
| CN101113018B (en) * | 2006-07-26 | 2011-03-30 | 黑龙江大学 | Preparation method of highlight catalytic active titanium oxide |
| CN102145920A (en) * | 2011-04-18 | 2011-08-10 | 东华大学 | Method for preparing oil-soluble anatase titanium dioxide nanoparticles with two-step process |
| CN102216221A (en) * | 2008-11-12 | 2011-10-12 | 日产化学工业株式会社 | Titanium oxide sol manufacturing method |
| CN102250484A (en) * | 2011-05-20 | 2011-11-23 | 常州有则科技有限公司 | Carbazolyl organic dye used for dye-sensitized solar cells and preparation method thereof |
| CN103771505A (en) * | 2012-10-24 | 2014-05-07 | 中国石油化工股份有限公司 | Synthetic method of titanium dioxide self-assembled particles |
| CN105170097A (en) * | 2015-09-29 | 2015-12-23 | 安徽工程大学 | TiO2/ZIF-8 nanocomposite with core-shell structure and preparation method of TiO2/ZIF-8 nanocomposite |
| CN107123693A (en) * | 2017-04-14 | 2017-09-01 | 华南理工大学 | A kind of efficient CdTe nanometer crystalline solar cell with high transparency window layer material processed based on solwution method and preparation method thereof |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB9501086D0 (en) * | 1995-01-20 | 1995-03-08 | Tioxide Group Services Ltd | Preparation of anatase titanium dioxide |
| DE10205920A1 (en) * | 2002-02-12 | 2003-08-21 | Itn Nanovation Gmbh | Nanoscale rutile and process for its production |
| CN1184002C (en) * | 2002-05-21 | 2005-01-12 | 中国科学院化学研究所 | Prepn. method for producing titanium dioxide having visible light catalytic activation |
| CN1194900C (en) * | 2003-01-13 | 2005-03-30 | 复旦大学 | Preparation method of crystal phase controllable titanium dioxide nanometer crystal |
| CN1276876C (en) * | 2003-09-17 | 2006-09-27 | 上海工程技术大学 | Process for preparing nanometer titanium dioxide |
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2005
- 2005-11-17 CN CNB2005101104460A patent/CN1317194C/en not_active Expired - Fee Related
Cited By (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101113018B (en) * | 2006-07-26 | 2011-03-30 | 黑龙江大学 | Preparation method of highlight catalytic active titanium oxide |
| CN100583463C (en) * | 2007-11-28 | 2010-01-20 | 中国科学院上海硅酸盐研究所 | Production method for titanium oxide coating material in dye sensitized solar battery |
| US8802159B2 (en) | 2008-11-12 | 2014-08-12 | Nissan Chemical Industries, Ltd. | Production method of titanium oxide sol |
| CN102216221A (en) * | 2008-11-12 | 2011-10-12 | 日产化学工业株式会社 | Titanium oxide sol manufacturing method |
| CN102216221B (en) * | 2008-11-12 | 2014-09-10 | 日产化学工业株式会社 | Titanium oxide sol manufacturing method |
| CN101982417A (en) * | 2010-09-27 | 2011-03-02 | 彩虹集团公司 | Preparation method of titanium dioxide nanocrystalline sol |
| CN102145920A (en) * | 2011-04-18 | 2011-08-10 | 东华大学 | Method for preparing oil-soluble anatase titanium dioxide nanoparticles with two-step process |
| CN102145920B (en) * | 2011-04-18 | 2012-11-07 | 东华大学 | Method for preparing oil-soluble anatase titanium dioxide nanoparticles with two-step process |
| CN102250484A (en) * | 2011-05-20 | 2011-11-23 | 常州有则科技有限公司 | Carbazolyl organic dye used for dye-sensitized solar cells and preparation method thereof |
| CN103771505A (en) * | 2012-10-24 | 2014-05-07 | 中国石油化工股份有限公司 | Synthetic method of titanium dioxide self-assembled particles |
| CN103771505B (en) * | 2012-10-24 | 2015-08-12 | 中国石油化工股份有限公司 | A kind of synthetic method of titanium dioxide self-assembly particle |
| CN105170097A (en) * | 2015-09-29 | 2015-12-23 | 安徽工程大学 | TiO2/ZIF-8 nanocomposite with core-shell structure and preparation method of TiO2/ZIF-8 nanocomposite |
| CN107123693A (en) * | 2017-04-14 | 2017-09-01 | 华南理工大学 | A kind of efficient CdTe nanometer crystalline solar cell with high transparency window layer material processed based on solwution method and preparation method thereof |
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