CN102324316A - Compound light anode and preparation method thereof - Google Patents

Compound light anode and preparation method thereof Download PDF

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Publication number
CN102324316A
CN102324316A CN 201110210556 CN201110210556A CN102324316A CN 102324316 A CN102324316 A CN 102324316A CN 201110210556 CN201110210556 CN 201110210556 CN 201110210556 A CN201110210556 A CN 201110210556A CN 102324316 A CN102324316 A CN 102324316A
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tio
nano
graphene
wire array
light anode
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CN102324316B (en
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丁建宁
于成涛
袁宁一
刘跃斌
樊勇
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Nantong Donghu International Travel Agency Co., Ltd
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Changzhou University
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    • YGENERAL 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
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02EREDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E10/00Energy generation through renewable energy sources
    • Y02E10/50Photovoltaic [PV] energy
    • Y02E10/542Dye sensitized solar cells
    • YGENERAL 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
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02EREDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E10/00Energy generation through renewable energy sources
    • Y02E10/50Photovoltaic [PV] energy
    • Y02E10/549Organic PV cells

Abstract

The invention relates to a dye sensitization nanometer crystal solar battery, and in particular relates to a compound light anode and a preparation method thereof. The compound light anode is characterized in that a TiO2 seed crystal layer is covered on a graphene sheet and taken as a templet so as to grow a TiO2 nanometer line array, and a nanometer grain is grown on the nanometer line array so as to form a composite structure, and the compound light anode is applied in a dye sensitization solar battery; the graphene sheet is covered on FTO (tin oxide) glass as a blocked layer so as to prevent the FTO glass and the electrolyte from directly contacting with each other, a TiO2 nanometer grain layer is covered on the graphene sheet to serve as the seed crystal of the TiO2 nanometer line array, and the nanometer line array is grown by a hydrothermal method; the nanometer grain grown on the nanometer line array can be used for increasing the specific area of the light anode, and the adsorptive capacity of a dye is increased, thereby improving the photocurrent and conversion efficiency of DSSC ( dye sensitized solar cells).

Description

A kind of complex light anode and preparation method thereof
Technical field
The present invention relates to the dye sensitized nano crystal solar cell, refer in particular to a kind of complex light anode and preparation method thereof; Complex light anode of the present invention is on graphene film, to cover TiO 2Inculating crystal layer is template growth TiO 2Nano-wire array and on nano-wire array the growing nano particle form composite construction, can be applicable in the DSSC.
Background technology
The shortage of non-renewable energies such as oil, coal, natural gas makes energy crisis day by day become one of restraining factors of social development, economic development and scientific technological advance, and the material that taps a new source of energy is key subjects that the our times various countries must at first solve with utilizing new forms of energy; And solar energy have cleaning, safe in utilization, inexhaustible, utilize cost low and do not receive plurality of advantages such as geographical conditions restriction, be the desirable energy that solves the energy and environmental problem; Dye sensitized nano crystal solar cell (DSSC) is based on a kind of novel solar cell that Nano-technology Development is got up; Has cost of manufacture low (its cost be merely silicon solar cell 1/5 ~ 1/10); Production technology is simple, pollution-free; Insensitive to variations in temperature and intensity variation, good light stability is a kind of extremely promising environment protection solar cell.
The porous nano crystallized semiconductor thin film that DSSC is mainly covered by transparent conduction base sheet, dyestuff, electrolyte solution and electrode formed.After receiving optical excitation; Dye molecule is from the ground state transition to excitation state, and the dyestuff that is in excitation state is injected into electronics in the conduction band of semiconductor nano, and the electronics that is injected in the conduction band transmits in semiconductor film; After arriving semiconductor film and electro-conductive glass contact-making surface, get into external circuit; The oxidation-reduction potential of oxidation-reduction pair poor in semi-conductive quasi-Fermi level and the electrolyte solution when open circuit photovoltage of DSSC is illumination; Short-circuit photocurrent depends on light capture rate, electron injection efficiency and the electric transmission efficient of light-sensitive coloring agent, and the resistance of reduction charge recombination effect and conduction band substrate of glass can improve fill factor, curve factor.
At present; How to make DSSC obtain higher photoelectric conversion efficiency; Improve stability test; Increase the service life is the hot issue of research always, and the compound of the capture rate of dyestuff adsorbance, light and the conduction of accelerated electron and inhibition electronics is three key factors that improve the electricity conversion of DSSC; Development along with nanometer technology; In DSSC, Graphene and monodimension nanometer material (like nano wire, nanotube etc.) have good electron-transporting to novel nano material with its good performance applications; Electronics is separated with the hole, suppress the generation of dark current.
Because Graphene has fabulous conductivity, there is report to utilize Graphene and TiO recently 2Nanocrystalline produced with combination light anode is used for the making of DSSC; Report in the ACS NANO magazine in 2010 like people such as Yang, at TiO 2In mix 0.6 % Graphene make the light anode, the short-circuit current density of DSSC is by 11.25 mA/cm 2Bring up to 16.29 mA/cm 2Open circuit voltage does not reduce; Transformation efficiency is brought up to 6.97 % (Yang NL, Zhai J, Wang D. Two-Dimensional Graphene Bridges Enhanced Photoinduced Charge Transport in Dye-Sensitized Solar Cells. ACS NANO by 5.01 %; 2010,4 (2): 380-386); People such as Kim are reported at Chemical Physics Letters magazine in 2009, at the GS/TiO of FTO glass surface spin coating one deck 500 nm 2Composite material, this one deck composite layer is not only at FTO glass and TiO 2Nano particle plays barrier layer, and has quickened the transfer of electronics, reduces at FTO/TiO 2Dark current between the interface; Open circuit voltage has increased by 54 mV; Electricity conversion is increased to 5.26 % (S. R. Kim from 4.89 %; M. K. Parvez, M. Chhowalla. UV-reduction of graphene oxide and its application as an interfacial layer to reduce the back-transport reactions in dye-sensitized solar cells. Chemical Physics Letters, 2009; 483,124-127.).
One-dimensional nano structure has superior electronics to separate and conductibility, and its length is on micron order, it is thus clear that scattering of light and absorbent properties greatly strengthen; Human hydrothermal methods such as Aydil obtain TiO 2It is lower that nano-wire array obtains efficient, the nano-wire array process TiCl that 4 μ m are long 4Obtain the transformation efficiency of 3 % after the aqueous solution is handled, Aydil is low owing to TiO efficient 2The specific area of array is little, causes not enough (the B. Liu and E. S. Aydil. Growth of Oriented Single-Crystalline Rutile TiO of dyestuff that adsorbs 2Nanorods on Transparent Conducting Substrates for Dye-Sensitized Solar Cells [J]. J. Am. Chem. Soc., 2009,131 (11), 3985-3990.); In order to remedy the little deficiency of nano-wire array surface area, tree-shaped/ZnO nanoparticle structure that people such as Wu have constructed the ZnO nanometer also is applied in the DSSC, and the compound of 3.5 μ m length has obtained the transformation efficiency of 3.74 %, is superior to TiO 2The battery of nano particle assembling because the existence of nano particle makes the adsorbance of dyestuff increase, thereby has increased electricity conversion.(C.?T.?Wu,?W.?P.?Liao,?J.?J.?Wu.?Three-dimensional?ZnO?nanodendrite/nanoparticle?composite?solar?cells[J].?Journal?of?Materials?Chemistry,?2011,?21,?2871-2876.)
The present invention proposes to utilize Graphene, TiO first for this reason 2Nano-wire array, TiO 2Nano particle is constructed a kind of light anode of composite construction of three-dimensional, covers a layer graphene and TiO at the FTO glass surface 2The composite construction film of nano particle is as barrier layer, and the TiO that grows above that 2Nano-wire array and TiO 2The composite construction of nano particle is through Graphene and TiO 2The transmission speed of the raising electronics of nano wire reduces the compound again of electric charge, thereby reaches the purpose that improves cell photoelectric time electric current and DSSC efficient.
Summary of the invention
The present invention proposes a kind of NEW TYPE OF COMPOSITE light anode material, i.e. Graphene/TiO 2Nano-wire array/TiO 2The nano particle composite construction is used for the making of DSSC.
It is on glass as barrier layer that the lamella of Graphene covers FTO, stops FTO glass to contact with the direct of electrolyte, on the lamella of Graphene, covers one deck TiO 2Nano particle is as growth TiO 2The seed crystal of nano-wire array, the Hydrothermal Growth nano-wire array, and the growing nano particle increases the specific area of light anode on nano-wire array, increases the adsorbance of dyestuff, thereby improves photoelectric current and the conversion efficiency of DSSC.
Realize that technical scheme of the present invention is:
The first step: at FTO even covering one layer graphene on glass/TiO 2Nanometer particle film with it as barrier layer, TiO 2Nano particle is as growth TiO 2The seed crystal of nano-wire array;
Second step: on the FTO sheet glass, utilize Hydrothermal Growth TiO 2Nano-wire array;
The 3rd step: at TiO 2Adhere to TiO on the nano-wire array 2Nano particle;
The 4th step: the composite construction for preparing is calcined under nitrogen atmosphere;
The 5th step: the sensitization of light anode and the assembling of battery.
The said method first step is characterized in that controlling the concentration of Graphene, i.e. graphene oxide and TiO 2Mass ratio, scope is 3% ~ 12%.
The said method first step is at FTO glass preparation Graphene/TiO 2Nanometer particle film refers to: at first prepare uniform and stable Graphene and TiO 2The nano particle composite solution is again with this Graphene and TiO 2It is on glass that the nano particle composite solution is spin-coated on FTO, makes Graphene and TiO 2Nano particle cover fully on the FTO sheet glass, at N 2Annealing obtains Graphene/TiO under the atmosphere 2Nanometer particle film; Or behind FTO first spin coating one layer graphene on glass spin coating TiO again 2Colloidal sol and at N 2Annealing obtains Graphene/TiO under the atmosphere 2Nanometer particle film.
The said method first step is at the Graphene/TiO of FTO covering on glass 2The thickness of nanometer particle film is below 200 nm;
Said second step of method, Hydrothermal Growth TiO 2The nano-wire array temperature range is at 120 ~ 200 ℃, and butyl titanate is as TiO 2The presoma of nano-wire array, its amount ranges are 1.4 * 10 -3-4.4 * 10 -3Mol;
Said the 3rd step of method is at TiO 2Adhere to TiO on the nano-wire array 2Nano particle, TiCl 4The concentration range of the aqueous solution is 0.05 ~ 0.4 M, and temperature range is at 30 ~ 90 ℃, and growth time is 0.5 ~ 48 h;
In said the 3rd step of method, adopt TiCl 4The aqueous solution is handled TiO 2Nano-wire array or at TiO 2Spin coating TiO on the nano-wire array 2The colloidal sol after annealing obtains TiO 2Nano-wire array/TiO 2The composite construction of nano particle;
In said the 4th step of method, the temperature range of sintering is 400 ~ 600 ℃, and time range is 10 ~ 60 min;
Advantage of the present invention adopts a kind of NEW TYPE OF COMPOSITE light anode material, i.e. Graphene/TiO first 2Nano-wire array/TiO 2Nano particle is used for the making of DSSC, in conjunction with Graphene and TiO 2The electron transport property of nano-wire array, TiO 2The specific area that nano particle is high had both been quickened the transfer of electronics, suppressed the generation of dark current, had increased the adsorbance of dyestuff again, thereby improved photoelectric current and the conversion efficiency of DSSC.
Description of drawings
Fig. 1 is earlier at the certain thickness Graphene/TiO of FTO spin-on-glass 2The nano particle composite bed, with it as the barrier layer between FTO glass and the electrolyte;
Fig. 2 is with TiO 2Nano particle is as seeded growth TiO 2Nano-wire array;
Fig. 3 is at last at TiO 2Load apposition growth TiO on the nano-wire array 2Nano particle, nano particle are filled between the nano-wire array;
Fig. 4 is the TiO of preparation in the instance one 2The SEM figure of nano-wire array, as can be seen from Figure 4 TiO 2It is on glass that nano-wire array is grown in FTO equably, but have bigger space between the nano wire, makes TiO 2The surface area ratio of nano-wire array is less;
Fig. 5 is the Graphene/TiO of preparation in the instance two 2Nano-particle complex is spin-coated on the AFM figure on the silicon chip, from Fig. 5 a, can find out spin coating Graphene/TiO one time 2Nano-particle complex can cover the surface of silicon chip equably, from Fig. 5 b, can find out spin coating Graphene/TiO one time 2The thickness of nano-particle complex is approximately 20 nm;
Fig. 6 is the Graphene/TiO of preparation in the instance four 2Nano-wire array/TiO 2The SEM figure of nano particle composite construction can significantly find out TiO from Fig. 6 2Nano-wire array is by TiO 2Nano particle is wrapped in, and has obviously reduced the space between the nano wire;
Fig. 7 is the I-V curve chart of battery sample in instance one, instance two, instance three and the instance four, can find out that from Fig. 7 the electricity conversion of battery of instance four is the highest, and instance one is the poorest.
Embodiment
Further specify content of the present invention below in conjunction with instance:
Instance one: TiO 2The preparation of nano-wire array sensitization battery
1, TiO 2The preparation of nano-wire array: utilize acetone, absolute ethyl alcohol and deionized water successively to the ultrasonic cleaning of FTO electro-conductive glass, the autoclave of 100 mL is put in oven dry, after getting 30 mL deionized waters and 30 mL concentrated hydrochloric acids and putting into beaker and stir 5 min; The butyl titanate that adds 1 mL, magnetic agitation 5 min pour in the agitated reactor solution for preparing airtight; Heating 20 h under 160 ℃ of temperature, reaction finishes the back takes out, and opens agitated reactor after being cooled to room temperature; Liquid is poured out; Take out sheet glass, find the film of growth one deck white on the sheet glass, film is TiO 2Nano-wire array;
2, the sensitization of electrode and battery assembling: because the TiO of growth 2Nano wire is a monocrystalline rutile phase, thus the not direct sensitization of sintering, 3 * 10 -4Soaking 24 h in the N719 dye solution of mol/L, process the light anode, is to electrode with the Pt electrode, is assembled into solar cell, and electrolyte is for containing 0.5 M LiI, 0.05 M I 2Acetonitrile solution with 0.5 M TBP (4-tert-butylpyridine).
Instance two: Graphene (GS)/TiO 2The preparation of nano-wire array sensitization battery
1, TiO 2The preparation of/GS compound: with TiCl 3Hydrochloric acid solution be the titanium source, the graphene oxide (GO) of 20 mg is dissolved in the deionized water of 150ml, regulating pH value is 10, after the ultrasonic dispersion, the polyvinylpyrrolidone (PVP) that adds 300mg stirs fully and dissolves, and drips the TiCl of 1 ml then 3Hydrochloric acid solution, magnetic agitation 90 ℃ the insulation 1 h after, obtain uniform and stable Graphene and TiO 2The nano particle composite solution;
2, the preparation of Graphene barrier layer: cleaned FTO spin-on-glass 5 times, make Graphene and TiO with above-mentioned solution 2Nano particle cover fully on the FTO sheet glass, at N 2Following 500 ℃ of 10 min that anneal down of atmosphere;
3, TiO 2The preparation of nano-wire array: with Graphene for preparing and TiO 2Nano particle cover the autoclave that the FTO sheet glass is put into 100 mL; After getting 30 mL deionized waters and 30 mL concentrated hydrochloric acids and putting into beaker and stir 5 min, add the butyl titanate of 1 mL, magnetic agitation 5 min; Pour in the agitated reactor solution for preparing airtight; Heating 20 h under 160 ℃ of temperature, reaction finishes the back takes out, and obtains nano-wire array;
4, the sensitization of electrode and battery assembling: with the sensitization and the assembling of battery in the instance one.
Instance three: TiO 2Nano-wire array/TiO 2The preparation of nanoparticle sensitized battery
1, TiO 2The preparation of nano-wire array: with TiO in the instance one 2The preparation of nano-wire array;
2, TiO 2The growth of nano particle: the TiO that above-mentioned growth is good 2Nano-wire array immerses the TiCl of 0.2 M 4In the aqueous solution, 30 ℃ of following insulation 24 h, reaction is accomplished the back and is taken out with absolute ethyl alcohol and clean, after at room temperature drying, 500 ℃ of 20 min that anneal down of nitrogen atmosphere;
3, the sensitization of electrode and battery assembling: with the sensitization and the assembling of battery in the instance one.
Instance four: Graphene/TiO 2Nano-wire array/TiO 2The preparation of nanoparticle sensitized battery
1, TiO 2The preparation of/GS compound: with TiCl 3Hydrochloric acid solution be the titanium source, the GO of 20 mg is dissolved in the deionized water of 150 mL, regulating pH value is 10, after the ultrasonic dispersion, the PVP that adds 300 mg stirs fully and dissolves, and drips the TiCl of 1 mL then 3Hydrochloric acid solution, magnetic agitation obtains all with stable Graphene and TiO behind 90 ℃ of insulation 1 h 2The nano particle composite solution;
2, the preparation of Graphene barrier layer: with the preparation of Graphene barrier layer in the instance two;
3, TiO 2The preparation of nano-wire array: with TiO in the instance two 2The preparation of nano-array;
4, TiO 2The growth of nano particle: with the growth of TiO2 nano particle in the instance three; .
5, the sensitization of electrode and battery assembling: with the sensitization and the assembling of battery in the instance one.
Implementation result:
At AM1.5,100 mW/cm 2Carry out the performance test of battery under the irradiation of etalon optical power.The battery of instance one preparation, open circuit voltage is 0.76V, short-circuit current density is 3.78 mA/cm 2, fill factor, curve factor 0.55, conversion efficiency is 1.59 %; The battery of the preparation of instance two, open circuit voltage are 0.77 V, and short-circuit current density is 5.23 mA/cm 2, fill factor, curve factor 0.65, conversion efficiency is 2.62 %; Wherein the raising of current density and fill factor, curve factor is apparent in view, and this mainly is that instance two is at the FTO layer graphene barrier layer of constructing on glass because on the basis of instance one; And utilize the quick conductibility of Graphene, it is on glass electronics to be transferred to FTO fast, reduces the generation of dark current; Improve fill factor, curve factor, increased current density; The battery of instance three preparations, open circuit voltage is 0.76 V, short-circuit current density is 10.47 mA/cm 2, fill factor, curve factor 0.56, conversion efficiency is 4.47 %; Open circuit voltage is 0.76 V in the instance four, and short-circuit current density is 17.06 mA/cm 2, fill factor, curve factor 0.62, conversion efficiency is 8.04 %.Than instance one, two and three, the conversion efficiency of instance four is maximum, and greater than the conversion efficiency sum of instance two and instance three, this explains Graphene, TiO 2Nano-wire array and TiO 2The composite construction of nano particle can be given full play to each clock material and get advantage, obviously improves the transformation efficiency of battery.

Claims (10)

1. complex light anode, it is characterized in that: said complex light anode is by Graphene/TiO 2The nano particle composite bed, TiO 2Nano-wire array and be filled in TiO 2TiO between the nano-wire array 2Nano particle is formed, Graphene/TiO 2TiO in the nano particle composite bed 2Growth obtains TiO to nano particle as inculating crystal layer 2Nano-wire array, Graphene/TiO 2Graphene in the nano particle composite bed is as the barrier layer of electrolyte.
2. the preparation method of a kind of complex light anode as claimed in claim 1 comprises the steps:
The first step: at the uniform Graphene/TiO of FTO preparation on glass 2Nanometer particle film with it as barrier layer, TiO 2Nano particle is as growth TiO 2The seed crystal of nano-wire array;
Second step: on the FTO sheet glass, utilize Hydrothermal Growth TiO 2Nano-wire array;
The 3rd step: at TiO 2Adhere to TiO on the nano-wire array 2Nano particle;
The 4th step: the composite construction for preparing is calcined under nitrogen atmosphere;
The 5th step: the sensitization of light anode and the assembling of battery.
3. the preparation method of a kind of complex light anode as claimed in claim 2 is characterized in that: the concentration of control Graphene, i.e. graphene oxide and TiO in the said step 1 2Mass ratio, scope is 3% ~ 12%.
4. the preparation method of a kind of complex light anode as claimed in claim 2 is characterized in that: in the said step 1 at FTO glass preparation Graphene/TiO 2Nanometer particle film refers to: at first prepare uniform and stable Graphene and TiO 2The nano particle composite solution is again with this Graphene and TiO 2It is on glass that the nano particle composite solution is spin-coated on FTO, makes Graphene and TiO 2Nano particle cover fully on the FTO sheet glass, at N 2Annealing obtains Graphene/TiO under the atmosphere 2Nanometer particle film; Or behind FTO first spin coating one layer graphene on glass spin coating TiO again 2Colloidal sol and at N 2Annealing obtains Graphene/TiO under the atmosphere 2Nanometer particle film.
5. the preparation method of a kind of complex light anode as claimed in claim 2 is characterized in that: in the said step 1 at the Graphene/TiO of FTO preparation on glass 2Nanometer particle film at thickness below 200 nm.
6. the preparation method of a kind of complex light anode as claimed in claim 2 is characterized in that: Hydrothermal Growth TiO in the said step 2 2The nano-wire array temperature range is at 120 ~ 200 ℃, and butyl titanate is as TiO 2The presoma of nano-wire array, its amount ranges are 1.4 * 10 -3-4.4 * 10 -3Mol.
7. the preparation method of a kind of complex light anode as claimed in claim 2 is characterized in that: adopt TiCl in the said step 3 4The aqueous solution is handled TiO 2Nano-wire array or at TiO 2Spin coating TiO on the nano-wire array 2The colloidal sol after annealing obtains TiO 2Nano-wire array/TiO 2The composite construction of nano particle.
8. the preparation method of a kind of complex light anode as claimed in claim 7 is characterized in that: adopt TiCl in the said step 3 4The aqueous solution is handled TiO 2Thereby nano-wire array is at TiO 2Adhere to TiO on the nano-wire array 2Nano particle, TiCl 4The concentration range of the aqueous solution is 0.05 ~ 0.4 M, and temperature range is at 30 ~ 90 ℃, and growth time is 0.5 ~ 48 h.
9. the preparation method of a kind of complex light anode as claimed in claim 2, it is characterized in that: the temperature range of sintering is 400 ~ 600 ℃ in the said step 4, time range is 10 ~ 60 min.
10. the application of a kind of complex light anode as claimed in claim 1 in the preparation of dye sensitized nano crystal solar cell.
CN 201110210556 2011-07-26 2011-07-26 Compound light anode and preparation method thereof Active CN102324316B (en)

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Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102700185A (en) * 2012-05-25 2012-10-03 清华大学 Preparation method of graphene oxide/titanium oxide layered composite film
CN102941078A (en) * 2012-11-16 2013-02-27 湖南大学 Compound titanium dioxide nanotube array photocatalyst and preparation method thereof
CN103030306A (en) * 2012-12-21 2013-04-10 延边万业隆新能源科技开发有限公司 Conducting glass, as well as preparation method and application thereof
CN103730260A (en) * 2013-12-30 2014-04-16 深圳大学 Dye-sensitized solar cell and preparation method of ZnO composite photo-anode of dye-sensitized solar cell
CN103887071A (en) * 2014-03-13 2014-06-25 四川材料与工艺研究所 Flexible nano paper-base compound photo-anode for dye-sensitized solar cell and preparation method thereof
CN104934108A (en) * 2014-12-31 2015-09-23 重庆元石石墨烯技术开发有限责任公司 Metallic nanowire-graphene bridge structural composite material and preparation method thereof
CN105788869A (en) * 2016-03-02 2016-07-20 常州大学 Preparation method for ultrathin quasi-solid dye sensitized cell

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20100294350A1 (en) * 2009-05-25 2010-11-25 Ko Min-Jae Photo-electrode comprising conductive non-metal film, and dye-sensitized solar cell comprising the same
CN101901693A (en) * 2010-07-29 2010-12-01 中国科学院宁波材料技术与工程研究所 Graphene composite dye-sensitized solar cell light anode and preparation method thereof

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20100294350A1 (en) * 2009-05-25 2010-11-25 Ko Min-Jae Photo-electrode comprising conductive non-metal film, and dye-sensitized solar cell comprising the same
CN101901693A (en) * 2010-07-29 2010-12-01 中国科学院宁波材料技术与工程研究所 Graphene composite dye-sensitized solar cell light anode and preparation method thereof

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CN102700185A (en) * 2012-05-25 2012-10-03 清华大学 Preparation method of graphene oxide/titanium oxide layered composite film
CN102941078B (en) * 2012-11-16 2014-10-15 湖南大学 Compound titanium dioxide nanotube array photocatalyst and preparation method thereof
CN102941078A (en) * 2012-11-16 2013-02-27 湖南大学 Compound titanium dioxide nanotube array photocatalyst and preparation method thereof
CN103030306A (en) * 2012-12-21 2013-04-10 延边万业隆新能源科技开发有限公司 Conducting glass, as well as preparation method and application thereof
CN103030306B (en) * 2012-12-21 2015-06-10 深圳市万业隆太阳能科技有限公司 Conducting glass, as well as preparation method and application thereof
CN103730260A (en) * 2013-12-30 2014-04-16 深圳大学 Dye-sensitized solar cell and preparation method of ZnO composite photo-anode of dye-sensitized solar cell
CN103730260B (en) * 2013-12-30 2016-11-02 深圳大学 DSSC and ZnO complex light anode preparation method thereof
CN103887071A (en) * 2014-03-13 2014-06-25 四川材料与工艺研究所 Flexible nano paper-base compound photo-anode for dye-sensitized solar cell and preparation method thereof
CN103887071B (en) * 2014-03-13 2016-09-14 四川材料与工艺研究所 A kind of flexible dye-sensitized solar battery nanometer paper substrate complex light anode and preparation method thereof
CN104934108A (en) * 2014-12-31 2015-09-23 重庆元石石墨烯技术开发有限责任公司 Metallic nanowire-graphene bridge structural composite material and preparation method thereof
CN104934108B (en) * 2014-12-31 2017-07-21 重庆元石石墨烯技术开发有限责任公司 Metal nanometer line-graphene portal structure composite and preparation method thereof
CN105788869A (en) * 2016-03-02 2016-07-20 常州大学 Preparation method for ultrathin quasi-solid dye sensitized cell
CN105788869B (en) * 2016-03-02 2019-11-12 常州大学 A kind of preparation method of ultra-thin quasi- solid-state sensitized cells

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