CN113436890B - Environment-friendly doped photo-anode sensitized by zinc-silver-indium-selenium quantum dots, preparation method thereof and photoelectrochemical cell - Google Patents
Environment-friendly doped photo-anode sensitized by zinc-silver-indium-selenium quantum dots, preparation method thereof and photoelectrochemical cell Download PDFInfo
- Publication number
- CN113436890B CN113436890B CN202110731699.9A CN202110731699A CN113436890B CN 113436890 B CN113436890 B CN 113436890B CN 202110731699 A CN202110731699 A CN 202110731699A CN 113436890 B CN113436890 B CN 113436890B
- Authority
- CN
- China
- Prior art keywords
- silver
- zinc
- indium
- titanium dioxide
- environment
- 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.)
- Active
Links
- -1 zinc-silver-indium-selenium quantum dots Chemical class 0.000 title claims abstract description 54
- 238000002360 preparation method Methods 0.000 title claims abstract description 32
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 claims abstract description 144
- 239000004408 titanium dioxide Substances 0.000 claims abstract description 72
- 239000002096 quantum dot Substances 0.000 claims abstract description 65
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims abstract description 44
- 229910021389 graphene Inorganic materials 0.000 claims abstract description 44
- 238000000034 method Methods 0.000 claims abstract description 25
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims abstract description 17
- 230000004888 barrier function Effects 0.000 claims abstract description 17
- 229910052725 zinc Inorganic materials 0.000 claims abstract description 17
- 239000011701 zinc Substances 0.000 claims abstract description 17
- 239000000203 mixture Substances 0.000 claims abstract description 10
- 229910052709 silver Inorganic materials 0.000 claims abstract description 7
- 239000004332 silver Substances 0.000 claims abstract description 7
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 claims abstract description 6
- 229910052738 indium Inorganic materials 0.000 claims abstract description 3
- APFVFJFRJDLVQX-UHFFFAOYSA-N indium atom Chemical compound [In] APFVFJFRJDLVQX-UHFFFAOYSA-N 0.000 claims abstract description 3
- 239000000243 solution Substances 0.000 claims description 76
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 52
- 238000010438 heat treatment Methods 0.000 claims description 39
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims description 36
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims description 36
- 239000002002 slurry Substances 0.000 claims description 22
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 20
- SQGYOTSLMSWVJD-UHFFFAOYSA-N silver(1+) nitrate Chemical compound [Ag+].[O-]N(=O)=O SQGYOTSLMSWVJD-UHFFFAOYSA-N 0.000 claims description 20
- 239000000758 substrate Substances 0.000 claims description 20
- BUGBHKTXTAQXES-UHFFFAOYSA-N Selenium Chemical compound [Se] BUGBHKTXTAQXES-UHFFFAOYSA-N 0.000 claims description 18
- 238000006243 chemical reaction Methods 0.000 claims description 18
- 239000011521 glass Substances 0.000 claims description 18
- 239000002904 solvent Substances 0.000 claims description 18
- 238000000151 deposition Methods 0.000 claims description 17
- 239000011259 mixed solution Substances 0.000 claims description 17
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 17
- ZOIORXHNWRGPMV-UHFFFAOYSA-N acetic acid;zinc Chemical compound [Zn].CC(O)=O.CC(O)=O ZOIORXHNWRGPMV-UHFFFAOYSA-N 0.000 claims description 16
- 239000004246 zinc acetate Substances 0.000 claims description 16
- 230000008021 deposition Effects 0.000 claims description 14
- 238000001035 drying Methods 0.000 claims description 14
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 claims description 12
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 12
- 239000008367 deionised water Substances 0.000 claims description 12
- 229910021641 deionized water Inorganic materials 0.000 claims description 12
- 239000006185 dispersion Substances 0.000 claims description 12
- 239000007788 liquid Substances 0.000 claims description 12
- 239000002243 precursor Substances 0.000 claims description 12
- 229910052711 selenium Inorganic materials 0.000 claims description 12
- 239000011669 selenium Substances 0.000 claims description 12
- 229910052717 sulfur Inorganic materials 0.000 claims description 12
- 239000011593 sulfur Substances 0.000 claims description 12
- WNAHIZMDSQCWRP-UHFFFAOYSA-N dodecane-1-thiol Chemical compound CCCCCCCCCCCCS WNAHIZMDSQCWRP-UHFFFAOYSA-N 0.000 claims description 11
- 239000003960 organic solvent Substances 0.000 claims description 11
- VBXWCGWXDOBUQZ-UHFFFAOYSA-K diacetyloxyindiganyl acetate Chemical compound [In+3].CC([O-])=O.CC([O-])=O.CC([O-])=O VBXWCGWXDOBUQZ-UHFFFAOYSA-K 0.000 claims description 10
- 229910052757 nitrogen Inorganic materials 0.000 claims description 10
- 238000002161 passivation Methods 0.000 claims description 10
- 229910001961 silver nitrate Inorganic materials 0.000 claims description 10
- GRVFOGOEDUUMBP-UHFFFAOYSA-N sodium sulfide (anhydrous) Chemical compound [Na+].[Na+].[S-2] GRVFOGOEDUUMBP-UHFFFAOYSA-N 0.000 claims description 10
- 239000006228 supernatant Substances 0.000 claims description 10
- 238000004140 cleaning Methods 0.000 claims description 9
- 230000008569 process Effects 0.000 claims description 9
- 229910052979 sodium sulfide Inorganic materials 0.000 claims description 9
- WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 claims description 8
- 239000011248 coating agent Substances 0.000 claims description 8
- 238000000576 coating method Methods 0.000 claims description 8
- 238000001962 electrophoresis Methods 0.000 claims description 8
- 238000002156 mixing Methods 0.000 claims description 8
- CCCMONHAUSKTEQ-UHFFFAOYSA-N octadecene Natural products CCCCCCCCCCCCCCCCC=C CCCMONHAUSKTEQ-UHFFFAOYSA-N 0.000 claims description 8
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 claims description 8
- 239000002244 precipitate Substances 0.000 claims description 8
- 238000007493 shaping process Methods 0.000 claims description 8
- GEHJYWRUCIMESM-UHFFFAOYSA-L sodium sulfite Chemical compound [Na+].[Na+].[O-]S([O-])=O GEHJYWRUCIMESM-UHFFFAOYSA-L 0.000 claims description 8
- 239000002270 dispersing agent Substances 0.000 claims description 7
- 239000003446 ligand Substances 0.000 claims description 7
- 238000004528 spin coating Methods 0.000 claims description 7
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 claims description 6
- QGLWBTPVKHMVHM-KTKRTIGZSA-N (z)-octadec-9-en-1-amine Chemical compound CCCCCCCC\C=C/CCCCCCCCN QGLWBTPVKHMVHM-KTKRTIGZSA-N 0.000 claims description 6
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 claims description 6
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 claims description 6
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 claims description 6
- 239000005642 Oleic acid Substances 0.000 claims description 6
- 238000001354 calcination Methods 0.000 claims description 6
- 238000007872 degassing Methods 0.000 claims description 6
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 claims description 6
- 238000000465 moulding Methods 0.000 claims description 6
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 claims description 6
- 238000010345 tape casting Methods 0.000 claims description 6
- 238000001132 ultrasonic dispersion Methods 0.000 claims description 6
- 239000003792 electrolyte Substances 0.000 claims description 5
- 238000005086 pumping Methods 0.000 claims description 5
- 229910021607 Silver chloride Inorganic materials 0.000 claims description 4
- 238000001652 electrophoretic deposition Methods 0.000 claims description 4
- 239000012046 mixed solvent Substances 0.000 claims description 4
- 229910052697 platinum Inorganic materials 0.000 claims description 4
- 239000001103 potassium chloride Substances 0.000 claims description 4
- 235000011164 potassium chloride Nutrition 0.000 claims description 4
- 238000004321 preservation Methods 0.000 claims description 4
- HKZLPVFGJNLROG-UHFFFAOYSA-M silver monochloride Chemical compound [Cl-].[Ag+] HKZLPVFGJNLROG-UHFFFAOYSA-M 0.000 claims description 4
- 238000002791 soaking Methods 0.000 claims description 4
- 235000010265 sodium sulphite Nutrition 0.000 claims description 4
- 238000005406 washing Methods 0.000 claims description 4
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 claims description 2
- 238000000861 blow drying Methods 0.000 claims description 2
- 150000003342 selenium Chemical class 0.000 claims description 2
- 238000004513 sizing Methods 0.000 claims description 2
- 238000009210 therapy by ultrasound Methods 0.000 claims description 2
- 238000004506 ultrasonic cleaning Methods 0.000 claims 1
- 238000010521 absorption reaction Methods 0.000 abstract description 2
- 229920006395 saturated elastomer Polymers 0.000 abstract description 2
- 239000002131 composite material Substances 0.000 abstract 1
- 125000003748 selenium group Chemical class *[Se]* 0.000 abstract 1
- 230000002194 synthesizing effect Effects 0.000 abstract 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 7
- 229910052739 hydrogen Inorganic materials 0.000 description 7
- 239000001257 hydrogen Substances 0.000 description 7
- 239000012295 chemical reaction liquid Substances 0.000 description 4
- 230000018044 dehydration Effects 0.000 description 4
- 238000006297 dehydration reaction Methods 0.000 description 4
- 239000013110 organic ligand Substances 0.000 description 4
- 238000010791 quenching Methods 0.000 description 4
- 239000002994 raw material Substances 0.000 description 4
- 239000000725 suspension Substances 0.000 description 4
- 238000000862 absorption spectrum Methods 0.000 description 3
- 230000008859 change Effects 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 238000005516 engineering process Methods 0.000 description 3
- 238000011056 performance test Methods 0.000 description 3
- 239000010405 anode material Substances 0.000 description 2
- 229910052793 cadmium Inorganic materials 0.000 description 2
- BDOSMKKIYDKNTQ-UHFFFAOYSA-N cadmium atom Chemical compound [Cd] BDOSMKKIYDKNTQ-UHFFFAOYSA-N 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 231100000331 toxic Toxicity 0.000 description 2
- 230000002588 toxic effect Effects 0.000 description 2
- 230000009286 beneficial effect Effects 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 238000005868 electrolysis reaction Methods 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 229910001385 heavy metal Inorganic materials 0.000 description 1
- 231100000086 high toxicity Toxicity 0.000 description 1
- 238000005286 illumination Methods 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 239000002105 nanoparticle Substances 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 238000010248 power generation Methods 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 238000005215 recombination Methods 0.000 description 1
- 230000006798 recombination Effects 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 239000004065 semiconductor Substances 0.000 description 1
Images
Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01G—CAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES, LIGHT-SENSITIVE OR TEMPERATURE-SENSITIVE DEVICES OF THE ELECTROLYTIC TYPE
- H01G9/00—Electrolytic capacitors, rectifiers, detectors, switching devices, light-sensitive or temperature-sensitive devices; Processes of their manufacture
- H01G9/20—Light-sensitive devices
- H01G9/2027—Light-sensitive devices comprising an oxide semiconductor electrode
- H01G9/2036—Light-sensitive devices comprising an oxide semiconductor electrode comprising mixed oxides, e.g. ZnO covered TiO2 particles
-
- 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
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P70/00—Climate change mitigation technologies in the production process for final industrial or consumer products
- Y02P70/50—Manufacturing or production processes characterised by the final manufactured product
Landscapes
- Engineering & Computer Science (AREA)
- Power Engineering (AREA)
- Microelectronics & Electronic Packaging (AREA)
- Hybrid Cells (AREA)
Abstract
The invention discloses an environment-friendly doped photo-anode sensitized by zinc, silver, indium and selenium quantum dots, a preparation method thereof and a photoelectrochemical cell, wherein the method comprises the following steps: (1) preparing a titanium dioxide barrier layer; (2) preparing a titanium dioxide composite photo-anode doped with graphene oxide; (3) synthesizing environment-friendly zinc-silver-indium-selenium quantum dots; (4) preparing a quantum dot sensitized photoanode; (5) and passivating the surface of the photoanode. By the preparation method provided by the invention, the environment-friendly zinc-silver-indium-selenium quantum dots are used for the sensitized photoanode, and the absorption range of the sensitized photoanode to light can be remarkably improved. And the graphene oxide is doped in the titanium dioxide electrode, so that the transfer rate of electrons in the electrode can be improved, the composition of photo-generated electrons and holes in the electrode is inhibited, the performance of the photoelectrochemical cell is obviously improved, and the saturated photocurrent density of the photoelectrochemical cell can reach 6.5mA/cm under the irradiation of standard simulated sunlight 2 。
Description
Technical Field
The invention belongs to the technical field of photochemical batteries, and particularly relates to an environment-friendly zinc-silver-indium-selenium quantum dot sensitized doped photo-anode, a preparation method thereof and a photoelectrochemical battery.
Background
Photoelectrochemical cells are cells made using semiconductor-liquid junctions that can directly use light energy and convert it into a clean renewable hydrogen energy source, alleviating the energy crisis. The photoelectrochemical cell is composed of a photoelectrode with optical activity, electrolyte and an external circuit, is simple in structure, and has lower device cost compared with a technology of producing hydrogen by photovoltaic power generation and water electrolysis. Among them, semiconductor titanium dioxide is often used as an anode material of a photoelectrochemical cell because of its good stability and appropriate energy band position. However, the large band gap (-3.2 eV) of titanium dioxide causes that titanium dioxide can only utilize part of ultraviolet light in sunlight, seriously influences the conversion efficiency of light energy to hydrogen energy, and the problem can be overcome well by introducing quantum dots with wide absorption spectrum range to sensitize the titanium dioxide photo anode. In addition, the hydrogen production technology of the quantum dot sensitized photoelectrochemical cell cannot be put into practical application in a large scale at present and is limited to the following aspects: firstly, the traditional quantum dot sensitized doped photo-anode material contains toxic metal elements such as lead and cadmium, and is not beneficial to the development of the technology from the aspects of environmental protection and commercialization; secondly, the activity and stability of the environment-friendly photoelectrode material which is researched are low; thirdly, the photoelectrode material has a limited absorption range of sunlight, and the near infrared part cannot be effectively utilized; fourth, the conventional photoelectrode is formed by stacking titanium dioxide nanoparticles, and photo-generated electrons are easily recombined with holes when being transferred at a titanium dioxide interface, which finally results in the reduction of the photoelectrochemical conversion efficiency.
Disclosure of Invention
The invention aims to provide an environment-friendly zinc-silver-indium-selenium quantum dot sensitized doped photo-anode, a preparation method thereof and a photoelectrochemical cell, which can solve a series of problems of high toxicity, narrow absorption spectrum range and low activity of a quantum dot photoelectrochemical cell in the prior art.
In order to achieve the aim, the invention provides a preparation method of an environment-friendly zinc-silver-indium-selenium quantum dot sensitized doped photo-anode, which comprises the following steps:
(1) preparation of titanium dioxide Barrier layer
Cleaning and blow-drying a substrate, spin-coating a titanium-nano oxide solution on the substrate, and then calcining to prepare a titanium dioxide barrier layer;
(2) preparation of graphene oxide doped titanium dioxide photoanode
Mixing ethanol dispersion liquid of graphene oxide, titanium dioxide slurry and a dispersing agent, performing ultrasonic treatment, and pumping to 1/5 of the volume of the original mixture under a vacuum condition to obtain slurry; coating the slurry on the titanium dioxide barrier layer prepared in the step (1), and preparing a graphene oxide doped titanium dioxide photo-anode through molding, sizing, heating and heat preservation;
(3) synthetic environment-friendly zinc-silver-indium-selenium quantum dot
Dissolving zinc acetate, silver nitrate and indium acetate in a mixed organic solvent to obtain a reaction solution, adding a selenium precursor solution into the reaction solution, heating and preserving heat until quantum dots completely grow to obtain a zinc-silver-indium-selenium quantum dot solution;
(4) preparation of quantum dot sensitized photoanode
Mixing the zinc-silver-indium-selenium quantum dot solution with an organic solvent, shaking and centrifuging to obtain a supernatant, adding ethanol into the supernatant, centrifuging to obtain a precipitate, and dissolving the precipitate in toluene to obtain a deposition solution; constructing an electrophoresis device by using the graphene oxide doped titanium dioxide anode and the deposition solution for electrophoretic deposition to obtain an environment-friendly zinc-silver-indium-selenium quantum dot sensitized graphene oxide doped titanium dioxide photoanode;
(5) photoanode surface passivation
And (4) sequentially placing the photoanode prepared in the step (4) in a zinc source and a sulfur source for soaking for 45-75s, then washing and drying, and repeating the steps of soaking, washing and drying for 1-2 times.
Further, the substrate is FTO conductive glass, and the cleaning comprises the steps of respectively placing the substrate in acetone, ethanol and deionized water, ultrasonically cleaning for 20-40min, and drying by using nitrogen.
Further, the coating of the step (1) is spin coating at the rotating speed of 4000-.
Further, the mixing ratio of the ethanol dispersion liquid of graphene oxide, the dispersing agent and the titanium dioxide slurry is 1-3 mL: 1-2 mL: 1-2g, the concentration of the ethanol dispersion liquid of the graphene oxide is 0.1mg/mL, and the ultrasonic time is 20-40 min.
Further, the thickness of the film coated on the titanium dioxide barrier layer by the slurry is 10-15 μm, the process of molding, shaping, heating and heat preservation is that the slurry is firstly stood for 10-15min for tape casting molding at normal temperature, then heated for 5-7min for shaping at the temperature of 140 ℃ for 100-.
Further, the concentrations of zinc acetate, silver nitrate and indium acetate added into the solvent are respectively as follows: 0.025mol/L, 0.01mol/L and 0.025mol/L, wherein the mixed organic solvent is a mixture of octadecene and ligand, the volume ratio of the octadecene to the ligand is 8:1.0-1.2, and the ligand is a mixture of dodecyl mercaptan and oleic acid in a volume ratio of 1: 0.1-0.2; the selenium precursor solution is prepared by the following method: dissolving 0.05-0.06mmol selenium powder in a mixed solution of 0.4mL of dodecyl mercaptan and 1.0mL of oleylamine, and performing ultrasonic dispersion.
Further, the step (3) specifically comprises the following processes: adding a solvent and a ligand into zinc acetate, silver nitrate and indium acetate, degassing for 5-15min at 55-65 ℃ in vacuum, heating to 100-.
Further, the organic solvent in the step (4) comprises toluene or cyclohexane, the volume ratio of the zinc-silver-indium-selenium quantum dot solution to the organic solvent to the ethanol is 1-3:1-3:6-8, and the electrophoretic deposition method comprises the following steps: two graphene oxide-doped titanium dioxide anodes are taken as a working electrode and a counter electrode of the electrophoresis device respectively, the electrode distance is 1cm, the electrode area is 0.5cm x 1.0cm, the voltage is 200V, and the deposition time is 1-3 h.
Further, the zinc source is methanol solution of zinc acetate, and the concentration of the zinc source is 0.1 mol/L; the sulfur source is a solution with the concentration of 0.1mol/L obtained by dissolving sodium sulfide in a mixed solvent, the mixed solvent is obtained by equal-volume mixing of methanol and deionized water, and the rinsing process is rinsing by using a corresponding solvent.
The environment-friendly doped photo-anode sensitized by the zinc-silver-indium-selenium quantum dots is prepared by adopting the preparation method of the environment-friendly doped photo-anode sensitized by the zinc-silver-indium-selenium quantum dots.
A photoelectrochemical cell comprises an environment-friendly zinc-silver-indium-selenium quantum dot sensitized doped photoanode, a platinum counter electrode, a silver/silver chloride reference electrode of 3mol/L potassium chloride and an electrolyte of a mixed solution (pH is 13) of 0.25mol/L sodium sulfide and 0.35mol/L sodium sulfite.
In summary, the invention has the following advantages:
1. the quantum dots prepared by the method do not contain any toxic heavy metal elements (such as lead, cadmium and the like);
2. the absorption spectrum range of the photo-anode prepared by the invention can reach near-infrared wave band, and solar energy can be more effectively utilized;
3. according to the invention, the titanium dioxide electrode is doped with the graphene oxide, so that the resistance of electrons in the electrode is reduced, and the recombination of electrons and holes on the titanium dioxide interface is inhibited;
4. the performance of a photoelectrochemical cell equipped with the environment-friendly zinc-silver-indium-selenium quantum dot sensitized doped photoanode prepared by the method is obviously improved, and the saturated photocurrent density is up to 6.5mA/cm under the irradiation of simulated sunlight 2 (the performance of the titanium dioxide photo-anode is close to the highest value of the photo-anode of the similar near-infrared light electrochemical cell), compared with the performance of the titanium dioxide photo-anode sensitized by the zinc-silver-indium-selenium quantum dots without doped graphene oxide, is improved by 23%;
5. the photoelectrochemical cell equipped with the environment-friendly zinc-silver-indium-selenium quantum dot sensitized doped photo-anode prepared by the method has the hydrogen yield of 5.2 mu mol per 1 hour, and the hydrogen yield is improved by 79 percent compared with the yield of an electrode without doped graphene oxide;
6. the photoelectrochemical cell equipped with the environment-friendly zinc-silver-indium-selenium quantum dot sensitized doped photo-anode prepared by the method can keep 70% of stability of the photo-anode under 1-hour light-dark alternate irradiation, and is greatly improved compared with a titanium dioxide electrode which does not participate in graphene oxide.
Drawings
Fig. 1 is a photo-anode of oxidized graphene doped titanium dioxide sensitized by the environment-friendly zinc-silver-indium-selenium quantum dots prepared in example 1;
fig. 2 is a schematic structural diagram of an environment-friendly zinc-silver-indium-selenium quantum dot sensitized oxidized graphene doped titanium dioxide photoanode prepared in example 1;
fig. 3 is a current density-voltage curve of the environment-friendly zinc-silver-indium-selenium quantum dot sensitized oxidized graphene doped titanium dioxide photoanode prepared in example 1 under a standard simulated sunlight illumination condition.
Detailed Description
The principles and features of this invention are described below in conjunction with embodiments, which are included to explain the invention and not to limit the scope of the invention. The examples, in which specific conditions are not specified, were conducted under conventional conditions or conditions recommended by the manufacturer. The reagents or instruments used are not indicated by the manufacturer, and are all conventional products available commercially.
Example 1
The embodiment provides a preparation method of an environment-friendly zinc-silver-indium-selenium quantum dot sensitized doped photo-anode, which comprises the following steps:
(1) preparation of titanium dioxide Barrier layer
Cleaning the FTO conductive glass in acetone, ethanol and deionized water in sequence by ultrasonic waves for 30min respectively, and drying by using nitrogen; spin-coating a titanium-nano oxide (Ti-hydroxide BL/SC, the same below) solution on an FTO conductive glass substrate at a rotation speed of 5000r/min, and then putting the FTO conductive glass substrate into a muffle furnace to heat to 500 ℃ for calcination and keeping the temperature for 30min to prepare a titanium dioxide barrier layer;
(2) preparation of graphene oxide doped titanium dioxide photoanode
Firstly, preparing 0.1mg/mL of graphene oxide ethanol dispersion liquid, adding 1.5mL of the dispersion liquid into 1g of titanium dioxide slurry (18NR-AO), then adding 2mL of ethanol serving as a dispersing agent, and placing the mixture in ultrasonic waves for dispersing for 30 min; pumping the dispersed slurry mixed solution in vacuum to 1/5, and then coating the prepared graphene oxide doped titanium dioxide slurry on a calcined FTO glass substrate by a blade coating thickness of 14 μm; standing at normal temperature for 13min for tape casting, heating on a heating plate at 120 deg.C for 6min for shaping, and heating in a muffle furnace at a heating rate of 5 deg.C/min to 500 deg.C for 30 min.
(3) Synthetic environment-friendly zinc-silver-indium-selenium quantum dot
Firstly, preparing a precursor solution of selenium, and dissolving 0.54mmol of selenium powder in a mixed solution of 0.4mL of dodecyl mercaptan and 1.0mL of oleylamine for ultrasonic dispersion for later use; then putting 0.2mmol of zinc acetate, 0.08mmol of silver nitrate and 0.2mmol of indium acetate in a 50mL three-neck flask, adding 8mL of octadecene, 1mL of dodecanethiol and 100 mu L of oleic acid solution, degassing at 60 ℃ for 10min in vacuum, then heating to 120 ℃ for dehydration for 20min, and ensuring that the raw materials are completely dissolved and are clear and transparent; heating the solution to 175 ℃ at the heating rate of 2 ℃/min, preserving the temperature for 10min, then quickly injecting the precursor solution of selenium into the reaction solution, and keeping the reaction temperature at 175 ℃ for 40min to ensure that the quantum dots completely grow; finally placing the three-neck flask in cold water to quench the reaction, transferring the reaction liquid into a centrifuge tube to be collected, and refrigerating in a refrigerator at 4 ℃;
(4) preparation of quantum dot sensitized photoanode
Preparing a deposition solution, taking 2mL of zinc-silver-indium-selenium quantum dot solution, adding 2mL of toluene to fully dissolve quantum dots containing organic ligands into the solution, centrifuging at the rotating speed of 3500r/min for 3min to obtain supernatant, adding 7mL of ethanol into the supernatant to change the solution into suspension, fully oscillating, centrifuging at the rotating speed of 12000r/min for 3min to obtain precipitate, and re-dispersing in 8mL of toluene to obtain the deposition solution; taking two obtained graphene oxide doped titanium dioxide electrodes as a working electrode and a counter electrode of an electrophoresis device respectively, wherein the electrode distance is 1cm, the electrode area is about 0.5cm x 1.0cm, applying a voltage of 200V, and depositing for 2h to finally obtain an environment-friendly zinc-silver-indium-selenium quantum dot sensitized graphene oxide doped titanium dioxide photoanode;
(5) photoanode surface passivation
Preparing 0.1mol/L zinc acetate solution (the solvent is methanol) and 0.1mol/L sodium sulfide solution (the solvent is mixed solution of methanol and deionized water with equal volume) as a zinc source and a sulfur source, sequentially immersing the photoanode into the zinc source and the sulfur source for 1min respectively, then rinsing with the corresponding solvents and drying with nitrogen, recording the operation as one cycle, and carrying out two cycle operations in total in the whole passivation process.
The photoelectrochemical cell was constructed by using the environment-friendly type zinc-silver-indium-selenium quantum dot sensitized doped photoanode prepared in example 1 (shown in fig. 1-3) as an anode, silver/silver chloride of 3mol/L potassium chloride as a reference electrode, a mixed solution of 0.25mol/L sodium sulfide and 0.35mol/L sodium sulfite (pH 13) as an electrolyte, and a platinum counter electrode, and performance tests were performed using a standard am1.5g solar simulator as a light source, with the results shown in table 1.
Example 2
The embodiment provides a preparation method of an environment-friendly zinc-silver-indium-selenium quantum dot sensitized doped photo-anode, which comprises the following steps:
(1) preparation of a titanium dioxide Barrier layer
Cleaning the FTO conductive glass in acetone, ethanol and deionized water in sequence by ultrasonic waves for 30min respectively, and drying by using nitrogen; spin-coating a titanium-nano oxide solution on an FTO conductive glass substrate at a rotating speed of 5500r/min, then putting the FTO conductive glass substrate into a muffle furnace, heating to 550 ℃, calcining and keeping for 40min to prepare a titanium dioxide barrier layer;
(2) preparation of graphene oxide doped titanium dioxide photoanode
Firstly, preparing 0.1mg/mL of graphene oxide ethanol dispersion liquid, adding 2mL of the dispersion liquid into 2g of titanium dioxide slurry (18NR-AO), then adding 2mL of ethanol serving as a dispersing agent, and placing the mixture in ultrasonic waves for dispersing for 30 min; pumping the dispersed slurry mixed solution in vacuum to 1/5, and then coating the prepared graphene oxide doped titanium dioxide slurry on a calcined FTO glass substrate by a blade with the thickness of 12.2 mu m; standing at normal temperature for 15min for tape casting, heating on a heating plate at 120 deg.C for 6min for shaping, and heating in a muffle furnace at a heating rate of 5 deg.C/min to 500 deg.C for 30 min.
(3) Synthetic environment-friendly zinc-silver-indium-selenium quantum dot
Firstly, preparing a precursor solution of selenium, and dissolving 0.54mmol of selenium powder in a mixed solution of 0.4mL of dodecyl mercaptan and 1.0mL of oleylamine for ultrasonic dispersion for later use; then putting 0.2mmol of zinc acetate, 0.08mmol of silver nitrate and 0.2mmol of indium acetate in a 50mL three-neck flask, adding 8mL of octadecene, 1mL of dodecyl mercaptan and 200 mu L of oleic acid solution, degassing at 60 ℃ in vacuum for 10min, then heating to 120 ℃ for dehydration for 20min, and ensuring that the raw materials are completely dissolved and are clear and transparent; heating the solution to 175 ℃ at the heating rate of 2 ℃/min, preserving the temperature for 10min, then quickly injecting the precursor solution of selenium into the reaction solution, and maintaining the reaction temperature of 175 ℃ for 40min to ensure that the quantum dots completely grow; finally placing the three-neck flask in cold water to quench the reaction, transferring the reaction liquid into a centrifuge tube to be collected, and refrigerating in a refrigerator at 4 ℃;
(4) preparation of quantum dot sensitized photoanode
Firstly, preparing a deposition solution, taking 2mL of zinc-silver-indium-selenium quantum dot solution, adding 2mL of toluene to fully dissolve an organic ligand in the solution, adding 7mL of ethanol solution to obtain a suspension, fully oscillating, centrifuging to obtain a precipitate, and re-dispersing in 8mL of toluene to serve as the deposition solution; taking two obtained graphene oxide-doped titanium dioxide electrodes as a working electrode and a counter electrode of an electrophoresis device respectively, applying a voltage of 200V to deposit for 2h, wherein the electrode distance is 1cm, the electrode area is 0.5cm x 1.0cm, and finally obtaining an environment-friendly zinc-silver-indium-selenium quantum dot sensitized graphene oxide-doped titanium dioxide photoanode;
(5) photoanode surface passivation
Preparing 0.1mol/L zinc acetate solution (the solvent is methanol) and 0.1mol/L sodium sulfide solution (the solvent is mixed solution of methanol and deionized water with equal volume) as a zinc source and a sulfur source, sequentially immersing the photoanode into the zinc source and the sulfur source for 1min respectively, then rinsing with the corresponding solvents and drying with nitrogen, recording the operation as one cycle, and carrying out two cycle operations in total in the whole passivation process.
Example 3
The embodiment provides a preparation method of an environment-friendly zinc-silver-indium-selenium quantum dot sensitized doped photo-anode, which comprises the following steps:
(1) preparation of titanium dioxide Barrier layer
Cleaning the FTO conductive glass in acetone, ethanol and deionized water in sequence by ultrasonic waves for 30min respectively, and drying by using nitrogen; spin-coating a titanium-nano oxide solution on an FTO conductive glass substrate at the rotating speed of 5000r/min, then putting the FTO conductive glass substrate into a muffle furnace, heating to 600 ℃, calcining and keeping for 25min to prepare a titanium dioxide barrier layer;
(2) preparation of graphene oxide doped titanium dioxide photoanode
Firstly, preparing 0.1mg/mL of graphene oxide ethanol dispersion liquid, adding 2mL of the dispersion liquid into 1g of titanium dioxide slurry (18NR-AO), then adding 2mL of ethanol serving as a dispersing agent, and placing the mixture in ultrasonic waves for dispersing for 30 min; pumping the dispersed slurry mixed solution in vacuum to 1/5, and then coating the prepared graphene oxide doped titanium dioxide slurry on a calcined FTO glass substrate by a blade with the thickness of 10.5 mu m; standing at normal temperature for 13min for tape casting, heating on a heating plate at 120 deg.C for 6min for shaping, and heating in a muffle furnace at a heating rate of 5 deg.C/min to 500 deg.C for 30 min.
(3) Synthetic environment-friendly zinc-silver-indium-selenium quantum dot
Firstly, preparing a selenium precursor solution, and dissolving 0.54mmol of selenium powder in 0.4mL of decadithiol and 1.0mL of oleylamine mixed solution for ultrasonic dispersion for later use; then putting 0.2mmol of zinc acetate, 0.08mmol of silver nitrate and 0.2mmol of indium acetate in a 50mL three-neck flask, adding 8mL of octadecene, 1mL of dodecanethiol and 100 mu L of oleic acid solution, degassing at 60 ℃ for 10min in vacuum, then heating to 120 ℃ for dehydration for 20min, and ensuring that the raw materials are completely dissolved and are clear and transparent; heating the solution to 175 ℃ at the heating rate of 2 ℃/min, preserving the temperature for 10min, then quickly injecting the selenium precursor solution into the reaction solution, and maintaining the reaction temperature of 175 ℃ for 40min to ensure that the quantum dots completely grow; finally placing the three-neck flask in cold water to quench the reaction, transferring the reaction liquid into a centrifuge tube to be collected, and refrigerating in a refrigerator at 4 ℃;
(4) preparation of quantum dot sensitized photoanode
Preparing a deposition solution, taking 2mL of zinc-silver-indium-selenium quantum dot solution, adding 2mL of toluene to fully dissolve quantum dots containing organic ligands into the solution, centrifuging at the rotating speed of 3500r/min for 3min to obtain supernatant, adding 7mL of ethanol into the supernatant to change the solution into suspension, fully oscillating, centrifuging at the rotating speed of 12000r/min for 3min to obtain precipitate, and re-dispersing in 8mL of toluene to obtain the deposition solution; taking two obtained graphene oxide doped titanium dioxide electrodes as a working electrode and a counter electrode of an electrophoresis device respectively, wherein the electrode distance is 1cm, the electrode area is about 0.5cm x 1.0cm, applying a voltage of 200V, and depositing for 2h to finally obtain an environment-friendly zinc-silver-indium-selenium quantum dot sensitized graphene oxide doped titanium dioxide photoanode;
(5) photoanode surface passivation
Preparing 0.1mol/L zinc acetate solution (the solvent is methanol) and 0.1mol/L sodium sulfide solution (the solvent is mixed solution of methanol and deionized water with equal volume) as a zinc source and a sulfur source, sequentially immersing the photoanode into the zinc source and the sulfur source for 1min respectively, then rinsing with the corresponding solvents and drying with nitrogen, recording the operation as one cycle, and carrying out two cycle operations in total in the whole passivation process.
Comparative example 1
The comparative example provides another preparation method of an environment-friendly zinc-silver-indium-selenium quantum dot sensitized pure titanium dioxide photo-anode, which comprises the following steps:
(1) preparation of a titanium dioxide Barrier layer
Cleaning the FTO conductive glass in acetone, ethanol and deionized water in sequence by ultrasonic waves for 30min respectively, and drying by using nitrogen; spin-coating a titanium-nano oxide solution on an FTO conductive glass substrate at the rotating speed of 5000r/min, then putting the FTO conductive glass substrate into a muffle furnace, heating to 500 ℃, calcining and keeping for 30min to prepare a titanium dioxide barrier layer;
(2) preparation of pure titanium dioxide photoanode
Firstly, 1g of titanium dioxide slurry (18NR-AO) is blade-coated on a calcined FTO glass substrate to a blade coating thickness of 14 μm; standing at normal temperature for 13min for tape casting, heating on a heating plate at 120 deg.C for 6min for shaping, and heating in a muffle furnace at a heating rate of 5 deg.C/min to 500 deg.C for 30 min.
(3) Synthetic environment-friendly zinc-silver-indium-selenium quantum dot
Firstly, preparing a precursor solution of selenium, and dissolving 0.54mmol of selenium powder in a mixed solution of 0.4mL of dodecyl mercaptan and 1.0mL of oleylamine for ultrasonic dispersion for later use; then putting 0.2mmol of zinc acetate, 0.08mmol of silver nitrate and 0.2mmol of indium acetate in a 50mL three-neck flask, adding 8mL of octadecene, 1mL of dodecanethiol and 100 mu L of oleic acid solution, degassing at 60 ℃ for 10min in vacuum, then heating to 120 ℃ for dehydration for 20min, and ensuring that the raw materials are completely dissolved and are clear and transparent; heating the solution to 175 ℃ at the heating rate of 2 ℃/min, preserving the temperature for 10min, then quickly injecting the precursor solution of selenium into the reaction solution, and maintaining the reaction temperature of 175 ℃ for 40min to ensure that the quantum dots completely grow; finally, placing the three-neck flask in cold water to quench the reaction, transferring the reaction liquid into a centrifuge tube to be collected, and refrigerating in a refrigerator at 4 ℃;
(4) preparation of quantum dot sensitized photoanode
Preparing a deposition solution, taking 2mL of zinc-silver-indium-selenium quantum dot solution, adding 2mL of toluene to fully dissolve quantum dots containing organic ligands into the solution, centrifuging at the rotating speed of 3500r/min for 3min to obtain supernatant, adding 7mL of ethanol into the supernatant to change the solution into suspension, fully oscillating, centrifuging at the rotating speed of 12000r/min for 3min to obtain precipitate, and re-dispersing in 8mL of toluene to obtain the deposition solution; taking two obtained pure titanium dioxide electrodes as a working electrode and a counter electrode of an electrophoresis device respectively, wherein the electrode distance is 1cm, the electrode area is about 0.5cm x 1.0cm, applying a voltage of 200V, and depositing for 2h to obtain an environment-friendly pure titanium dioxide photo-anode sensitized by zinc, silver, indium and selenium quantum dots;
(5) photoanode surface passivation
Preparing 0.1mol/L zinc acetate solution (the solvent is methanol) and 0.1mol/L sodium sulfide solution (the solvent is mixed solution of methanol and deionized water with equal volume) as a zinc source and a sulfur source, sequentially immersing the photoanode into the zinc source and the sulfur source for 1min respectively, then rinsing with the corresponding solvents and drying with nitrogen, recording the operation as one cycle, and carrying out two cycle operations in total in the whole passivation process.
The environment-friendly zinc-silver-indium-selenium quantum dot sensitized pure titanium dioxide photoanode prepared in comparative example 1 is used as a photoanode, silver/silver chloride of 3mol/L potassium chloride is used as a reference electrode, a mixed solution of 0.25mol/L sodium sulfide and 0.35mol/L sodium sulfite (pH 13) is used as an electrolyte and a platinum counter electrode to jointly form a photoelectrochemical cell, and a standard AM1.5G solar simulator is used as a light source to perform photoelectrochemical performance tests. The results are shown in Table 1.
Table 1 photoelectrochemical cell performance test data
As can be seen from Table 1, the environment-friendly quantum dot sensitized graphene oxide doped titanium dioxide photo-anode prepared by the method has excellent photoelectrochemical properties and excellent stability, wherein the saturation photocurrent density is up to 6.5mA/cm under the irradiation of simulated sunlight 2 The performance of the titanium dioxide photo-anode sensitized by the zinc-silver-indium-selenium quantum dots which are similar to those of the titanium dioxide photo-anode not doped with the graphene oxide is improved by 23 percent; the hydrogen yield is 5.2 mu mol in 1 hour, which is improved by 79 percent compared with the electrode yield of the undoped graphene oxide; under the alternate irradiation of light and dark for 1 hour, the light anode can keep 70% of stability, and is greatly improved compared with a titanium dioxide electrode which is not doped with graphene oxide.
While the present invention has been described in detail with reference to the illustrated embodiments, it should not be construed as limited to the scope of the present patent. Various modifications and changes may be made by those skilled in the art without inventive step within the scope of the appended claims.
Claims (9)
1. A preparation method of an environment-friendly doped photo-anode sensitized by zinc, silver, indium and selenium quantum dots is characterized by comprising the following steps:
(1) preparation of titanium dioxide Barrier layer
Cleaning and blow-drying a substrate, spin-coating a titanium-nano oxide solution on the substrate, and then calcining to prepare a titanium dioxide barrier layer;
(2) preparation of graphene oxide doped titanium dioxide photoanode
Mixing ethanol dispersion liquid of graphene oxide, titanium dioxide slurry and a dispersing agent, performing ultrasonic treatment, and pumping to 1/5 of the volume of the original mixture under a vacuum condition to obtain slurry; coating the slurry on the titanium dioxide barrier layer prepared in the step (1), and preparing a graphene oxide doped titanium dioxide photo-anode through molding, sizing, heating and heat preservation;
the thickness of the film coated on the titanium dioxide barrier layer by the slurry is 10-15 μm, the process of molding, shaping, heating and heat preservation is that the slurry is firstly stood for 10-15min for tape casting molding at normal temperature, then heated for 5-7min for shaping at the temperature of 140 ℃ of 100-;
(3) synthetic environment-friendly zinc-silver-indium-selenium quantum dot
Dissolving zinc acetate, silver nitrate and indium acetate in a mixed organic solvent to obtain a reaction solution, then adding a selenium precursor solution into the reaction solution, heating and preserving heat until quantum dots completely grow to obtain a zinc-silver-indium-selenium quantum dot solution;
(4) preparation of quantum dot sensitized photoanode
Mixing the zinc-silver-indium-selenium quantum dot solution with an organic solvent, shaking and centrifuging to obtain a supernatant, adding ethanol into the supernatant, centrifuging to obtain a precipitate, and dissolving the precipitate in toluene to obtain a deposition solution; constructing an electrophoresis device by using the graphene oxide doped titanium dioxide anode and the deposition solution for electrophoretic deposition to obtain an environment-friendly zinc-silver-indium-selenium quantum dot sensitized graphene oxide doped titanium dioxide photoanode;
(5) photoanode surface passivation
And (5) sequentially placing the photoanode prepared in the step (4) in a zinc source and a sulfur source for soaking for 45-75s, then washing and drying, and repeating the steps of soaking, washing and drying for 1-2 times.
2. The method for preparing an environment-friendly zinc-silver-indium-selenium quantum dot sensitized doped photoanode as claimed in claim 1, wherein the substrate is FTO conductive glass, and the cleaning comprises sequentially placing the substrate in acetone, ethanol and deionized water for ultrasonic cleaning for 20-40min, and drying by using nitrogen.
3. The method for preparing the environment-friendly zinc-silver-indium-selenium quantum dot sensitized doped photoanode as claimed in claim 1, wherein the mixing ratio of the ethanol dispersion of graphene oxide, the dispersing agent and the titanium dioxide slurry is 1-3 mL: 1-2 mL: 1-2g, wherein the concentration of the ethanol dispersion liquid of the graphene oxide is 0.1mg/mL, and the ultrasonic time is 20-40 min.
4. The method for preparing an environment-friendly zinc-silver-indium-selenium quantum dot sensitized doped photo-anode according to claim 1, wherein the concentrations of zinc acetate, silver nitrate and indium acetate added into a solvent are respectively as follows: 0.025mol/L, 0.01mol/L and 0.025mol/L, wherein the mixed organic solvent is a mixture of octadecene and a ligand, and the volume ratio of the octadecene solvent to the ligand is 8:1.0-1.2, wherein the ligand is a mixture of dodecyl mercaptan and oleic acid in a volume ratio of 1: 0.1-0.2; the selenium precursor solution is prepared by the following method: dissolving 0.05-0.06mmol selenium powder in a mixed solution of 0.4mL of dodecyl mercaptan and 1.0mL of oleylamine, and performing ultrasonic dispersion.
5. The method for preparing an environment-friendly zinc-silver-indium-selenium quantum dot sensitized doped photo-anode according to claim 1, wherein the step (3) specifically comprises the following steps: adding a mixed organic solvent into zinc acetate, silver nitrate and indium acetate, degassing for 5-15min at 55-65 ℃ in vacuum, heating to 100-.
6. The method for preparing an environment-friendly doped photoanode sensitized by zinc-silver-indium-selenium quantum dots according to claim 1, wherein the organic solvent in the step (4) comprises toluene or cyclohexane, the volume ratio of the zinc-silver-indium-selenium quantum dot solution to the organic solvent to ethanol is 1-3:1-3:6-8, and the electrophoretic deposition method comprises the following steps: two graphene oxide doped titanium dioxide photoanodes are taken as a working electrode and a counter electrode of the electrophoresis device respectively, the electrode distance is 1cm, the electrode area is 0.5cm x 1.0cm, the voltage is 200V, and the deposition time is 1-3 h.
7. The method for preparing an environment-friendly zinc-silver-indium-selenium quantum dot sensitized doped photo-anode according to claim 1, wherein the zinc source is a methanol solution of zinc acetate, and the concentration of the zinc source is 0.1 mol/L; the sulfur source is a solution with the concentration of 0.1mol/L obtained by dissolving sodium sulfide in a mixed solvent, the mixed solvent is obtained by equal-volume mixing of methanol and deionized water, and the rinsing process is rinsing by using a corresponding solvent.
8. The environment-friendly zinc-silver-indium-selenium quantum dot sensitized doped photoanode prepared by the preparation method of the environment-friendly zinc-silver-indium-selenium quantum dot sensitized doped photoanode as claimed in any one of claims 1 to 7.
9. A photoelectrochemical cell comprising a photoanode, a platinum counter electrode, a 3mol/L silver/silver chloride reference electrode of potassium chloride and an electrolyte of a mixed solution of 0.25mol/L sodium sulphide and 0.35mol/L sodium sulphite (pH 13); wherein the photo-anode is the environment-friendly doped photo-anode sensitized by the zinc-silver-indium-selenium quantum dots as claimed in claim 8.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN202110731699.9A CN113436890B (en) | 2021-06-29 | 2021-06-29 | Environment-friendly doped photo-anode sensitized by zinc-silver-indium-selenium quantum dots, preparation method thereof and photoelectrochemical cell |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN202110731699.9A CN113436890B (en) | 2021-06-29 | 2021-06-29 | Environment-friendly doped photo-anode sensitized by zinc-silver-indium-selenium quantum dots, preparation method thereof and photoelectrochemical cell |
Publications (2)
Publication Number | Publication Date |
---|---|
CN113436890A CN113436890A (en) | 2021-09-24 |
CN113436890B true CN113436890B (en) | 2022-08-30 |
Family
ID=77757871
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN202110731699.9A Active CN113436890B (en) | 2021-06-29 | 2021-06-29 | Environment-friendly doped photo-anode sensitized by zinc-silver-indium-selenium quantum dots, preparation method thereof and photoelectrochemical cell |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN113436890B (en) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN114597070B (en) * | 2022-03-21 | 2023-11-24 | 电子科技大学长三角研究院(湖州) | Photo-anode based on AgInSe/ZnSe core-shell structure quantum dots, and preparation method and application thereof |
CN115353882B (en) * | 2022-04-06 | 2023-09-05 | 电子科技大学长三角研究院(湖州) | Manganese-alloyed silver-indium-sulfur/copper-doped zinc sulfide quantum dot material, and preparation method and application thereof |
Citations (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102874799A (en) * | 2012-09-25 | 2013-01-16 | 南京工业大学 | Method for preparing graphene and titanium dioxide composite material by gas phase reduction method |
CN103440993A (en) * | 2013-08-30 | 2013-12-11 | 奇瑞汽车股份有限公司 | Method for improving efficiency of dye-sensitized solar cell |
CN103881723A (en) * | 2012-12-20 | 2014-06-25 | 深圳先进技术研究院 | Silver-doped zinc selenide quantum-dot, preparation method and applications thereof |
CN103896331A (en) * | 2014-03-08 | 2014-07-02 | 哈尔滨工程大学 | Method for preparing two-dimensional TiO2 nanometer material through template method |
CN104966617A (en) * | 2015-07-22 | 2015-10-07 | 陕西理工学院 | Composite photoanode for quantum dot sensitized solar cell and manufacturing method |
CN110085428A (en) * | 2019-05-14 | 2019-08-02 | 南京邮电大学 | A kind of compound light anode of titanium dioxide/graphene and preparation method thereof |
CN110993357A (en) * | 2019-12-24 | 2020-04-10 | 陕西理工大学 | CdS1-xSexPreparation method of alloy quantum dot sensitized photoanode |
CN111755254A (en) * | 2020-05-08 | 2020-10-09 | 电子科技大学 | Photoanode based on silver-indium-sulfur quantum dot sensitization, photoelectrochemical cell and preparation method |
CN113861984A (en) * | 2021-10-30 | 2021-12-31 | 重庆医科大学 | Preparation method of dual-emission quantum dot and application of dual-emission quantum dot in biological imaging |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2012050621A1 (en) * | 2010-10-15 | 2012-04-19 | Los Alamos National Security, Llc | Quantum dot sensitized solar cell |
-
2021
- 2021-06-29 CN CN202110731699.9A patent/CN113436890B/en active Active
Patent Citations (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102874799A (en) * | 2012-09-25 | 2013-01-16 | 南京工业大学 | Method for preparing graphene and titanium dioxide composite material by gas phase reduction method |
CN103881723A (en) * | 2012-12-20 | 2014-06-25 | 深圳先进技术研究院 | Silver-doped zinc selenide quantum-dot, preparation method and applications thereof |
CN103440993A (en) * | 2013-08-30 | 2013-12-11 | 奇瑞汽车股份有限公司 | Method for improving efficiency of dye-sensitized solar cell |
CN103896331A (en) * | 2014-03-08 | 2014-07-02 | 哈尔滨工程大学 | Method for preparing two-dimensional TiO2 nanometer material through template method |
CN104966617A (en) * | 2015-07-22 | 2015-10-07 | 陕西理工学院 | Composite photoanode for quantum dot sensitized solar cell and manufacturing method |
CN110085428A (en) * | 2019-05-14 | 2019-08-02 | 南京邮电大学 | A kind of compound light anode of titanium dioxide/graphene and preparation method thereof |
CN110993357A (en) * | 2019-12-24 | 2020-04-10 | 陕西理工大学 | CdS1-xSexPreparation method of alloy quantum dot sensitized photoanode |
CN111755254A (en) * | 2020-05-08 | 2020-10-09 | 电子科技大学 | Photoanode based on silver-indium-sulfur quantum dot sensitization, photoelectrochemical cell and preparation method |
CN113861984A (en) * | 2021-10-30 | 2021-12-31 | 重庆医科大学 | Preparation method of dual-emission quantum dot and application of dual-emission quantum dot in biological imaging |
Non-Patent Citations (2)
Title |
---|
Broad spectrum photoluminescent quaternary quantum dots for cell and animal imaging;Dawei Deng et al;《Chem. Commun》;20130814;第49卷;参见摘要,补充信息 * |
氧化石墨烯(GO)修饰的TiO2 纳米管阵列光阳极的制备及其在染料敏化太阳能电池(DSSC)中的应用;张泽铭;《广东化工》;20141231;第41卷(第14期);第10-11,17页 * |
Also Published As
Publication number | Publication date |
---|---|
CN113436890A (en) | 2021-09-24 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
Juang et al. | Energy harvesting under dim-light condition with dye-sensitized and perovskite solar cells | |
Theerthagiri et al. | Synthesis and characterization of (Ni1− xCox) Se2 based ternary selenides as electrocatalyst for triiodide reduction in dye-sensitized solar cells | |
Chen et al. | Dextran based highly conductive hydrogel polysulfide electrolyte for efficient quasi-solid-state quantum dot-sensitized solar cells | |
CN113436890B (en) | Environment-friendly doped photo-anode sensitized by zinc-silver-indium-selenium quantum dots, preparation method thereof and photoelectrochemical cell | |
CN101901693A (en) | Graphene composite dye-sensitized solar cell light anode and preparation method thereof | |
CN108493297B (en) | Preparation method of three-dimensional hollow selenium nickel sulfide nano-frame catalyst | |
Zhang et al. | Novel bilayer structure ZnO based photoanode for enhancing conversion efficiency in dye-sensitized solar cells | |
CN111755254B (en) | Photoanode based on silver-indium-sulfur quantum dot sensitization, photoelectrochemical cell and preparation method | |
CN106128772B (en) | A kind of preparation method of vulcanized lead quantum dot photovoltaic battery | |
Li et al. | Flexible quantum dot-sensitized solar cells with improved efficiencies based on woven titanium wires | |
CN108172401A (en) | Dye-sensitized cell combined counter electrode and its preparation method and application | |
CN108492994B (en) | It is a kind of to vulcanize witch culture conductive polythiophene to the preparation method of electrode for dye-sensitized solar cells | |
CN104377036A (en) | Method for preparing AgInS2 quantum dot sensitized TiO2 photoelectrode with In2S3 used as buffer layer | |
Wang et al. | Application of ZIF-67 based nitrogen-rich carbon frame with embedded Cu and Co bimetallic particles in QDSSCs | |
CN107799316A (en) | A kind of PbS quantum is sensitized TiO2The preparation method and applications of film | |
CN102254702A (en) | Composite light anode material and application thereof to dye sensitized cell preparation | |
Gulen | Lithium perchlorate-assisted electrodeposition of CoS catalyst surpassing the performance of platinum in dye sensitized solar cell | |
Yang et al. | High-performance electro-optical dual-control color-changing device based on WO3/Cu and TiO2/NiO/CdS composite electrodes | |
Bbumba et al. | How Components of Dye-sensitized Solar Cells Contribute to Efficient Solar Energy Capture | |
CN100541822C (en) | DSSC of a kind of nano-crystal film and preparation method thereof | |
CN105551811B (en) | The porous SnO of graded structure2And TiO2The Ag@C nanos ball of cladding, preparation method and applications | |
CN106847518B (en) | A kind of dye-sensitized solar cell anode and preparation method thereof | |
CN115064388A (en) | Dye-sensitive solar cell based on composite structure photo-anode and preparation method and application thereof | |
CN102930995A (en) | Quantum dot modified organic-inorganic hybrid solar cell and preparation method thereof | |
CN106803460A (en) | A kind of CuS for quantum dot sensitized solar cell is to electrode and preparation method thereof |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PB01 | Publication | ||
PB01 | Publication | ||
SE01 | Entry into force of request for substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
GR01 | Patent grant | ||
GR01 | Patent grant |