CN103021568A - Preparation method of dye-sensitized solar cell slurry - Google Patents
Preparation method of dye-sensitized solar cell slurry Download PDFInfo
- Publication number
- CN103021568A CN103021568A CN2012105286078A CN201210528607A CN103021568A CN 103021568 A CN103021568 A CN 103021568A CN 2012105286078 A CN2012105286078 A CN 2012105286078A CN 201210528607 A CN201210528607 A CN 201210528607A CN 103021568 A CN103021568 A CN 103021568A
- Authority
- CN
- China
- Prior art keywords
- ethyl cellulose
- slurry
- mixed slurry
- alcohol
- alcoholic solution
- 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.)
- Pending
Links
Classifications
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E10/00—Energy generation through renewable energy sources
- Y02E10/50—Photovoltaic [PV] energy
- Y02E10/542—Dye sensitized solar cells
Landscapes
- Crushing And Grinding (AREA)
Abstract
The invention relates to a preparation method of dye-sensitized solar cell slurry. The method includes adding ethyl cellulose into alcohol, stirring the mixture under magnetic force to enable the ethyl cellulose to be evenly dissolved and form alcohol solution of the ethyl cellulose, adding nano-grade power into the alcohol solution of the ethyl cellulose under normal temperature, stirring evenly under magnetic force to form mixed slurry A, adding terpineol into the mixed slurry under normal temperature, stirring evenly under magnetic force to form mixed slurry B, conducting ultrasonic dispersion on the mixed slurry B, increasing temperature of the mixed slurry B dispersed by ultrasonic dispersion to 35-40 DEG C, conducting rotating evaporation to remove alcohol and increasing temperature to 55-70 DEG C to conduct rotating evaporation to adjust slurry viscosity to requirements to obtain the dye-sensitized solar cell slurry. The preparation method is capable of strictly controlling slurry viscosity and simultaneously simplifying preparation process. The prepared dye-sensitized solar cell slurry is even in granularity.
Description
Technical field
The invention belongs to area of solar cell, be specifically related to a kind of preparation method of DSSC slurry.
Background technology
DSSC is simple because of manufacture craft, and relative low price probably becomes the leading of following solar cell.
Development along with DSSC, requirement to its material therefor and technology also further improves, preparing high performance DSSC slurry is the key that improves battery efficiency, and simplifying simultaneously preparation technology also is the important prerequisite that reduces cost and move towards industrialization.At present, the preparation technology of DSSC slurry is a bit loaded down with trivial details, effect neither be very good, generally before this about 80 ℃ and under the magnetic agitation, ethyl cellulose is dissolved in the saturating alcohol of turpentine oil, and then to its adding powder (or powder mixed liquor), rolling again after rough the stirring, this technique expense material of not only wasting time and energy, and the DSSC slurry that obtains at last is not too evenly (yet can stay the size particles of reuniting in various degree after the rolling) relatively, the slurry viscosity fluctuation is relatively large, and effect is not so good.
Summary of the invention
The present invention is directed to above deficiency, a kind of preparation method of DSSC slurry is provided.
In order to reach above-mentioned technical purpose, the technical solution used in the present invention may further comprise the steps:
1) at normal temperatures ethyl cellulose is joined in the alcohol then magnetic agitation dissolving, the alcoholic solution of formation ethyl cellulose;
2) at normal temperatures, nano level powder is joined in the alcoholic solution of ethyl cellulose, then magnetic agitation is even, forms mixed slurry A; Wherein, the mass ratio of the ethyl cellulose among the mixed slurry A in the alcoholic solution of nano level powder and ethyl cellulose is 1:(0.15-1.55), nano level powder is TiO
2, ZnO, CdSe, CdS, WO
3, Fe
2O
3, SnO
2, Graphene or gallium nitride;
3) at normal temperatures, the saturating alcohol of turpentine oil is added among the mixed slurry A, then magnetic agitation is even, forms mixed slurry B; Wherein, the mass ratio of the saturating alcohol of nano level powder and turpentine oil is 1:(1-14 among the mixed slurry B);
4) with repeatedly Ultrasonic Pulverization dispersion of mixed slurry B, make the granularity of the solid particle among the mixed slurry B below micron order;
5) the mixed slurry B after the Ultrasonic Pulverization dispersion is warming up to 35-40 ℃, revolves steaming and eliminate alcohol, then be warmed up to again 55-70 ℃ and revolve steaming adjusting slurry viscosity to necessary requirement, namely make the DSSC slurry.
The concentration of ethyl cellulose is 0.05g/mL in the alcoholic solution of described ethyl cellulose.
Because the solid bulky grain of reunion is arranged among the ultrasonic front mixed slurry B of the present invention, through after repeatedly ultrasonic, the solid bulky grain of reuniting is ground into below the micron order, and be dispersed among the mixed slurry B, mixed slurry B steams homogenizing through overwinding again, so the slurry that obtains does not at last need rolling, the DSSC slurry that makes is even, homogeneous grain diameter.In addition, the present invention can also recently determine to preset by the quality of adjusting raw material solid content and the viscosity of DSSC slurry.
The present invention is in order to regulate DSSC slurry uniformity and viscosity, and at first mixed slurry B is warming up to 35-40 ℃, revolves to steam to eliminate alcohol, then is raised to 55-70 ℃ again and revolves steaming adjusting slurry viscosity to preset value.Mixed slurry B of the present invention is when revolving steaming for 55-70 ℃, and each component of the organic carrier among the mixed slurry B is fully dissolved each other gradually, thereby reaches the purpose of regulating slurry viscosity.
Embodiment
Embodiment 1:
1) at normal temperatures ethyl cellulose is joined in the alcohol then magnetic agitation dissolving, the alcoholic solution of formation ethyl cellulose; Wherein, the concentration of ethyl cellulose is 0.05g/mL in the alcoholic solution of ethyl cellulose;
2) at normal temperatures, with nano level TiO
2Join in the alcoholic solution of ethyl cellulose, then magnetic agitation is even, forms mixed slurry A; Wherein, nano level TiO among the mixed slurry A
2With the mass ratio of ethyl cellulose in the alcoholic solution of ethyl cellulose be 1:0.15;
3) at normal temperatures, the saturating alcohol of turpentine oil is added among the mixed slurry A, then magnetic agitation is even, forms mixed slurry B; Wherein, nano level TiO among the mixed slurry B
2With turpentine oil thoroughly the mass ratio of alcohol be 1:10;
4) with mixed slurry B repeatedly Ultrasonic Pulverization disperse 3 times, make the granularity of the solid particle among the mixed slurry B below micron order;
5) the mixed slurry B after the Ultrasonic Pulverization dispersion is warming up to 35 ℃, revolves steaming and eliminate alcohol, then be warmed up to again 60 ℃ and revolve steaming adjusting slurry viscosity to necessary requirement, namely make the DSSC slurry.
Embodiment 2:
1) at normal temperatures ethyl cellulose is joined in the alcohol then magnetic agitation dissolving, the alcoholic solution of formation ethyl cellulose; Wherein, the concentration of ethyl cellulose is 0.05g/mL in the alcoholic solution of ethyl cellulose;
2) at normal temperatures, nano level Graphene is joined in the alcoholic solution of ethyl cellulose, then magnetic agitation is even, forms mixed slurry A; Wherein, the mass ratio of the ethyl cellulose in the alcoholic solution of nano level Graphene and ethyl cellulose is 1:0.5 among the mixed slurry A;
3) at normal temperatures, the saturating alcohol of turpentine oil is added among the mixed slurry A, then magnetic agitation is even, forms mixed slurry B; Wherein, the mass ratio of the saturating alcohol of nano level Graphene and turpentine oil is 1:1 among the mixed slurry B;
4) with mixed slurry B repeatedly Ultrasonic Pulverization disperse 5 times, make the granularity of the solid particle among the mixed slurry B below micron order;
5) the mixed slurry B after the Ultrasonic Pulverization dispersion is warming up to 38 ℃, revolves steaming and eliminate alcohol, then be warmed up to again 55 ℃ and revolve steaming adjusting slurry viscosity to necessary requirement, namely make the DSSC slurry.
Embodiment 3:
1) at normal temperatures ethyl cellulose is joined in the alcohol then magnetic agitation dissolving, the alcoholic solution of formation ethyl cellulose; Wherein, the concentration of ethyl cellulose is 0.05g/mL in the alcoholic solution of ethyl cellulose;
2) at normal temperatures, nano level ZnO is joined in the alcoholic solution of ethyl cellulose, then magnetic agitation is even, forms mixed slurry A; Wherein, the mass ratio of the ethyl cellulose in the alcoholic solution of nano level ZnO and ethyl cellulose is 1:0.70 among the mixed slurry A;
3) at normal temperatures, the saturating alcohol of turpentine oil is added among the mixed slurry A, then magnetic agitation is even, forms mixed slurry B; Wherein, the mass ratio of the saturating alcohol of nano level ZnO and turpentine oil is 1:4 among the mixed slurry B;
4) with mixed slurry B repeatedly Ultrasonic Pulverization disperse 4 times, make the granularity of the solid particle among the mixed slurry B below micron order;
5) the mixed slurry B after the Ultrasonic Pulverization dispersion is warming up to 40 ℃, revolves steaming and eliminate alcohol, then be warmed up to again 58 ℃ and revolve steaming adjusting slurry viscosity to necessary requirement, namely make the DSSC slurry.
Embodiment 4:
1) at normal temperatures ethyl cellulose is joined in the alcohol then magnetic agitation dissolving, the alcoholic solution of formation ethyl cellulose; Wherein, the concentration of ethyl cellulose is 0.05g/mL in the alcoholic solution of ethyl cellulose;
2) at normal temperatures, nano level CdSe is joined in the alcoholic solution of ethyl cellulose, then magnetic agitation is even, forms mixed slurry A; Wherein, the mass ratio of the ethyl cellulose in the alcoholic solution of nano level CdSe and ethyl cellulose is 1:1.55 among the mixed slurry A;
3) at normal temperatures, according to the saturating alcohol of turpentine oil is added among the mixed slurry A, then magnetic agitation is even, forms mixed slurry B; Wherein, the mass ratio of the saturating alcohol of nano level CdSe and turpentine oil is 1:14 among the mixed slurry B;
4) with mixed slurry B repeatedly Ultrasonic Pulverization disperse 6 times, make the granularity of the solid particle among the mixed slurry B below micron order;
5) the mixed slurry B after the Ultrasonic Pulverization dispersion is warming up to 40 ℃, revolves steaming and eliminate alcohol, then be warmed up to again 70 ℃ and revolve steaming adjusting slurry viscosity to necessary requirement, namely make the DSSC slurry.
Embodiment 5:
1) at normal temperatures ethyl cellulose is joined in the alcohol then magnetic agitation dissolving, the alcoholic solution of formation ethyl cellulose; Wherein, the concentration of ethyl cellulose is 0.05g/mL in the alcoholic solution of ethyl cellulose;
2) at normal temperatures, nano level gallium nitride is joined in the alcoholic solution of ethyl cellulose, then magnetic agitation is even, forms mixed slurry A; Wherein, the mass ratio of the ethyl cellulose in the alcoholic solution of nano level gallium nitride and ethyl cellulose is 1:1 among the mixed slurry A;
3) at normal temperatures, according to the saturating alcohol of turpentine oil is added among the mixed slurry A, then magnetic agitation is even, forms mixed slurry B; Wherein, the mass ratio of the saturating alcohol of nano level gallium nitride and turpentine oil is 1:14 among the mixed slurry B;
4) with mixed slurry B repeatedly Ultrasonic Pulverization disperse 6 times, make the granularity of the solid particle among the mixed slurry B below micron order;
5) the mixed slurry B after the Ultrasonic Pulverization dispersion is warming up to 40 ℃, revolves steaming and eliminate alcohol, then be warmed up to again 70 ℃ and revolve steaming adjusting slurry viscosity to necessary requirement, namely make the DSSC slurry.
Embodiment 6:
1) at normal temperatures ethyl cellulose is joined in the alcohol then magnetic agitation dissolving, the alcoholic solution of formation ethyl cellulose; Wherein, the concentration of ethyl cellulose is 0.05g/mL in the alcoholic solution of ethyl cellulose;
2) at normal temperatures, with nano level WO
3Join in the alcoholic solution of ethyl cellulose, then magnetic agitation is even, forms mixed slurry A; Wherein, nano level WO among the mixed slurry A
3With the mass ratio of ethyl cellulose in the alcoholic solution of ethyl cellulose be 1:1.2;
3) at normal temperatures, the saturating alcohol of turpentine oil is added among the mixed slurry A, then magnetic agitation is even, forms mixed slurry B; Wherein, nano level WO among the mixed slurry B
3With turpentine oil thoroughly the mass ratio of alcohol be 1:1;
4) with mixed slurry B repeatedly Ultrasonic Pulverization disperse 5 times, make the granularity of the solid particle among the mixed slurry B below micron order;
5) the mixed slurry B after the Ultrasonic Pulverization dispersion is warming up to 35 ℃, revolves steaming and eliminate alcohol, then be warmed up to again 70 ℃ and revolve steaming adjusting slurry viscosity to necessary requirement, namely make the DSSC slurry.
Embodiment 7:
1) at normal temperatures ethyl cellulose is joined in the alcohol then magnetic agitation dissolving, the alcoholic solution of formation ethyl cellulose; Wherein, the concentration of ethyl cellulose is 0.05g/mL in the alcoholic solution of ethyl cellulose;
2) at normal temperatures, nano level CdS is joined in the alcoholic solution of ethyl cellulose, then magnetic agitation is even, forms mixed slurry A; Wherein, the mass ratio of the ethyl cellulose in the alcoholic solution of nano level CdS and ethyl cellulose is 1:0.15 among the mixed slurry A;
3) at normal temperatures, the saturating alcohol of turpentine oil is added among the mixed slurry A, then magnetic agitation is even, forms mixed slurry B; Wherein, the mass ratio of the saturating alcohol of nano level CdS and turpentine oil is 1:9 among the mixed slurry B;
4) with mixed slurry B repeatedly Ultrasonic Pulverization disperse 5 times, make the granularity of the solid particle among the mixed slurry B below micron order;
5) the mixed slurry B after the Ultrasonic Pulverization dispersion is warming up to 40 ℃, revolves steaming and eliminate alcohol, then be warmed up to again 65 ℃ and revolve steaming adjusting slurry viscosity to necessary requirement, namely make the DSSC slurry.
Embodiment 8:
1) at normal temperatures ethyl cellulose is joined in the alcohol then magnetic agitation dissolving, the alcoholic solution of formation ethyl cellulose; Wherein, the concentration of ethyl cellulose is 0.05g/mL in the alcoholic solution of ethyl cellulose;
2) at normal temperatures, with nano level SnO
2Join in the alcoholic solution of ethyl cellulose, then magnetic agitation is even, forms mixed slurry A; Wherein, nano level SnO among the mixed slurry A
2With the mass ratio of ethyl cellulose in the alcoholic solution of ethyl cellulose be 1:0.5;
3) at normal temperatures, the saturating alcohol of turpentine oil is added among the mixed slurry A, then magnetic agitation is even, forms mixed slurry B; Wherein, nano level SnO among the mixed slurry B
2With turpentine oil thoroughly the mass ratio of alcohol be 1:13;
4) with mixed slurry B repeatedly Ultrasonic Pulverization disperse 3 times, make the granularity of the solid particle among the mixed slurry B below micron order;
5) the mixed slurry B after the Ultrasonic Pulverization dispersion is warming up to 35 ℃, revolves steaming and eliminate alcohol, then be warmed up to again 70 ℃ and revolve steaming adjusting slurry viscosity to necessary requirement, namely make the DSSC slurry.
Embodiment 9:
1) at normal temperatures ethyl cellulose is joined in the alcohol then magnetic agitation dissolving, the alcoholic solution of formation ethyl cellulose; Wherein, the concentration of ethyl cellulose is 0.05g/mL in the alcoholic solution of ethyl cellulose;
2) at normal temperatures, with nano level Fe
2O
3Join in the alcoholic solution of ethyl cellulose, then magnetic agitation is even, forms mixed slurry A; Wherein, nano level Fe among the mixed slurry A
2O
3With the mass ratio of ethyl cellulose in the alcoholic solution of ethyl cellulose be 1:0.3;
3) at normal temperatures, the saturating alcohol of turpentine oil is added among the mixed slurry A, then magnetic agitation is even, forms mixed slurry B; Wherein, nano level Fe among the mixed slurry B
2O
3With turpentine oil thoroughly the mass ratio of alcohol be 1:13;
4) with mixed slurry B repeatedly Ultrasonic Pulverization disperse 3 times, make the granularity of the solid particle among the mixed slurry B below micron order;
5) the mixed slurry B after the Ultrasonic Pulverization dispersion is warming up to 35 ℃, revolves steaming and eliminate alcohol, then be warmed up to again 70 ℃ and revolve steaming adjusting slurry viscosity necessary requirement, namely make the DSSC slurry.
The present invention at first takes out a little slurry and tests with viscosimeter when the control viscosity, if not to required viscosity then continue to revolve steaming, test again afterwards viscosity, until reach required viscosity, so just the slurry viscosity of wanting can be strictly controlled, also preparation technology can be simplified simultaneously.
Measure the fineness of DSSC slurry with Hegman grind gage, the bulky grain greater than 1 micron grain size does not exist, illustrate that powder granule size and distribution in the DSSC slurry are all very even, can be directly used in suitability for industrialized production, also simplified preparation technology simultaneously.
Claims (2)
1. the preparation method of a DSSC slurry is characterized in that may further comprise the steps:
1) at normal temperatures ethyl cellulose is joined in the alcohol then magnetic agitation dissolving, the alcoholic solution of formation ethyl cellulose;
2) at normal temperatures, nano level powder is joined in the alcoholic solution of ethyl cellulose, then magnetic agitation is even, forms mixed slurry A; Wherein, the mass ratio of the ethyl cellulose among the mixed slurry A in the alcoholic solution of nano level powder and ethyl cellulose is 1:(0.15-1.55), nano level powder is TiO
2, ZnO, CdSe, CdS, WO
3, Fe
2O
3, SnO
2, Graphene or gallium nitride;
3) at normal temperatures, the saturating alcohol of turpentine oil is added among the mixed slurry A, then magnetic agitation is even, forms mixed slurry B; Wherein, the mass ratio of the saturating alcohol of nano level powder and turpentine oil is 1:(1-14 among the mixed slurry B);
4) with repeatedly Ultrasonic Pulverization dispersion of mixed slurry B, make the granularity of the solid particle among the mixed slurry B below micron order;
5) the mixed slurry B after the Ultrasonic Pulverization dispersion is warming up to 35-40 ℃, revolves steaming and eliminate alcohol, then be warmed up to again 55-70 ℃ and revolve steaming adjusting slurry viscosity to necessary requirement, namely make the DSSC slurry.
2. the preparation method of DSSC slurry according to claim 1, it is characterized in that: the concentration of ethyl cellulose is 0.05g/mL in the alcoholic solution of described ethyl cellulose.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN2012105286078A CN103021568A (en) | 2012-12-10 | 2012-12-10 | Preparation method of dye-sensitized solar cell slurry |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN2012105286078A CN103021568A (en) | 2012-12-10 | 2012-12-10 | Preparation method of dye-sensitized solar cell slurry |
Publications (1)
Publication Number | Publication Date |
---|---|
CN103021568A true CN103021568A (en) | 2013-04-03 |
Family
ID=47970070
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN2012105286078A Pending CN103021568A (en) | 2012-12-10 | 2012-12-10 | Preparation method of dye-sensitized solar cell slurry |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN103021568A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN103354177A (en) * | 2013-07-18 | 2013-10-16 | 南京大学昆山创新研究院 | TiO2 slurry used in large-area dye-sensitized solar cell preparation by screen printing technology and method for preparing the TiO2 slurry |
CN109266315A (en) * | 2018-10-17 | 2019-01-25 | 中北大学 | A kind of preparation method of carbon dots base photothermal conversion materiat |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101174657A (en) * | 2007-11-28 | 2008-05-07 | 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 |
CN102074374A (en) * | 2011-02-14 | 2011-05-25 | 合肥工业大学 | Doping dye sensitized solar cell photo anode, preparation method and application thereof |
CN102176387A (en) * | 2011-03-02 | 2011-09-07 | 东莞宏威数码机械有限公司 | Methods for preparing porous spherical titanium dioxide paste and sensitized photo-anode |
CN102509624A (en) * | 2011-11-03 | 2012-06-20 | 东华大学 | Preparation of dye-sensitized solar battery from water-solubility and low-reactivity titanium source |
-
2012
- 2012-12-10 CN CN2012105286078A patent/CN103021568A/en active Pending
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101174657A (en) * | 2007-11-28 | 2008-05-07 | 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 |
CN102074374A (en) * | 2011-02-14 | 2011-05-25 | 合肥工业大学 | Doping dye sensitized solar cell photo anode, preparation method and application thereof |
CN102176387A (en) * | 2011-03-02 | 2011-09-07 | 东莞宏威数码机械有限公司 | Methods for preparing porous spherical titanium dioxide paste and sensitized photo-anode |
CN102509624A (en) * | 2011-11-03 | 2012-06-20 | 东华大学 | Preparation of dye-sensitized solar battery from water-solubility and low-reactivity titanium source |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN103354177A (en) * | 2013-07-18 | 2013-10-16 | 南京大学昆山创新研究院 | TiO2 slurry used in large-area dye-sensitized solar cell preparation by screen printing technology and method for preparing the TiO2 slurry |
CN103354177B (en) * | 2013-07-18 | 2015-11-04 | 南京大学昆山创新研究院 | A kind of TiO preparing large-area dye-sensitized solar battery for silk-screen printing technique 2slurry and preparation method thereof |
CN109266315A (en) * | 2018-10-17 | 2019-01-25 | 中北大学 | A kind of preparation method of carbon dots base photothermal conversion materiat |
CN109266315B (en) * | 2018-10-17 | 2020-11-03 | 中北大学 | Preparation method of carbon dot-based photothermal conversion material |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN100539205C (en) | Titanium dioxide nano-rod DSSC and preparation method thereof | |
CN107971502A (en) | A kind of preparation method of high dispersiveness spherical silver powder | |
CN105218836B (en) | A kind of method that emulsifying agent auxiliary biological enzyme prepares size tunable type starch nanometer granule | |
CN102924990A (en) | Transparent antireflection coating liquid and preparation method and application thereof | |
CN103943851B (en) | A kind of LiFePO4 aqueous positive-pole slurry and preparation method thereof | |
CN107042316A (en) | Front electrode of solar battery slurry silver powder and preparation method and application | |
CN102916168B (en) | Modification method of artificial graphite | |
CN102115994A (en) | Method for treating lignocellulose raw material | |
CN104376894A (en) | Solar cell conductive positive silver pulp | |
WO2018040569A1 (en) | Aluminum paste with high filling rate for local contact back surface field of perc cell and preparation method and use thereof | |
CN104475754A (en) | Preparation method of irregular flaky silver powder for silver slurry on back surface of solar cell | |
CN105018161A (en) | Slurry fuel prepared by baking biomass and application thereof | |
CN102543252B (en) | Silicon solar battery front silver paste with wide high-temperature sintering window | |
CN101412535A (en) | Preparation of nano titania slurry | |
CN106978170B (en) | A kind of preparation method of water-solubility fluorescent carbon quantum dot | |
CN104332591B (en) | A kind of lithium ion battery anode glue size and preparation technology thereof | |
CN103021568A (en) | Preparation method of dye-sensitized solar cell slurry | |
CN103394701B (en) | The preparation method of the super fine silver powder that a kind of epigranular is concentrated | |
CN107170962A (en) | A kind of lithium ion battery silicium cathode electrode slice and preparation method thereof | |
CN112086614B (en) | Lithium battery cathode batching process | |
CN106430209A (en) | Preparing method of mesoporous nano tungsten carbide and product | |
CN107331436B (en) | For carrying on the back the conducting aluminum paste and preparation method thereof of passivation solar battery | |
CN105632773B (en) | Method for improving photoelectric conversion efficiency of dye-sensitized solar cell | |
CN105869897B (en) | A kind of hollow material CeO2@TiO2Preparation method and applications | |
CN101783212A (en) | Conductive adhesive and preparation method of conductive porous membrane with large specific surface |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
C06 | Publication | ||
PB01 | Publication | ||
C10 | Entry into substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
C02 | Deemed withdrawal of patent application after publication (patent law 2001) | ||
WD01 | Invention patent application deemed withdrawn after publication |
Application publication date: 20130403 |