CN115512972A - Preparation method of quasi-solid electrolyte for quantum dot sensitized solar cell - Google Patents

Preparation method of quasi-solid electrolyte for quantum dot sensitized solar cell Download PDF

Info

Publication number
CN115512972A
CN115512972A CN202210994863.XA CN202210994863A CN115512972A CN 115512972 A CN115512972 A CN 115512972A CN 202210994863 A CN202210994863 A CN 202210994863A CN 115512972 A CN115512972 A CN 115512972A
Authority
CN
China
Prior art keywords
electrolyte
quasi
polysulfide
solar cell
solid
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.)
Granted
Application number
CN202210994863.XA
Other languages
Chinese (zh)
Other versions
CN115512972B (en
Inventor
李玲
张文明
王森阳
刘双安
樊娆
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Hebei University
Original Assignee
Hebei University
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Hebei University filed Critical Hebei University
Priority to CN202210994863.XA priority Critical patent/CN115512972B/en
Publication of CN115512972A publication Critical patent/CN115512972A/en
Application granted granted Critical
Publication of CN115512972B publication Critical patent/CN115512972B/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Images

Classifications

    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01GCAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES, LIGHT-SENSITIVE OR TEMPERATURE-SENSITIVE DEVICES OF THE ELECTROLYTIC TYPE
    • H01G9/00Electrolytic capacitors, rectifiers, detectors, switching devices, light-sensitive or temperature-sensitive devices; Processes of their manufacture
    • H01G9/20Light-sensitive devices
    • H01G9/2004Light-sensitive devices characterised by the electrolyte, e.g. comprising an organic electrolyte
    • H01G9/2009Solid electrolytes
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01GCAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES, LIGHT-SENSITIVE OR TEMPERATURE-SENSITIVE DEVICES OF THE ELECTROLYTIC TYPE
    • H01G9/00Electrolytic capacitors, rectifiers, detectors, switching devices, light-sensitive or temperature-sensitive devices; Processes of their manufacture
    • H01G9/0029Processes of manufacture
    • H01G9/0036Formation of the solid electrolyte layer
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01GCAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES, LIGHT-SENSITIVE OR TEMPERATURE-SENSITIVE DEVICES OF THE ELECTROLYTIC TYPE
    • H01G9/00Electrolytic capacitors, rectifiers, detectors, switching devices, light-sensitive or temperature-sensitive devices; Processes of their manufacture
    • H01G9/004Details
    • H01G9/04Electrodes or formation of dielectric layers thereon
    • H01G9/042Electrodes or formation of dielectric layers thereon characterised by the material
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M14/00Electrochemical current or voltage generators not provided for in groups H01M6/00 - H01M12/00; Manufacture thereof
    • H01M14/005Photoelectrochemical storage 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
    • Y02E10/542Dye sensitized solar cells

Landscapes

  • Engineering & Computer Science (AREA)
  • Power Engineering (AREA)
  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Electrochemistry (AREA)
  • Microelectronics & Electronic Packaging (AREA)
  • Materials Engineering (AREA)
  • Manufacturing & Machinery (AREA)
  • General Chemical & Material Sciences (AREA)
  • Hybrid Cells (AREA)
  • Photovoltaic Devices (AREA)

Abstract

The invention provides a preparation method of a quasi-solid electrolyte for a quantum dot sensitized solar cell. The method is simple to operate, and the quasi-solid polysulfide electrolyte is obtained by uniformly grinding the curing agent (sodium carboxymethylcellulose and polyvinylpyrrolidone) and the polysulfide electrolyte for a few times. The grinding method adopted by the invention is innovative in the electrolyte preparation process, the existing quasi-solid polysulfide electrolyte preparation method is changed, the grinding process is firstly used for preparing the quasi-solid electrolyte, the grinding method is novel and unique, the prepared quasi-solid electrolyte is convenient to store, the problem that the common polysulfide electrolyte is easy to leak is solved, and the problems that the mixing of a curing agent and the electrolyte is not uniform and not thorough caused by stirring and curing are also solved. The preparation method is simple and efficient, ensures the same photovoltaic performance as that of the common polysulfide electrolyte, and has good application value.

Description

Preparation method of quasi-solid electrolyte for quantum dot sensitized solar cell
Technical Field
The invention relates to the technical field of novel solar cells and energy, in particular to a preparation method of a quasi-solid electrolyte for a quantum dot sensitized solar cell.
Background
With the development of modern science and technology, the energy crisis and the environmental pollution problem become more severe, and the development of renewable energy is an urgent and difficult task. At present, the renewable energy sources mainly comprise water power, wind power, tidal power, biological energy, solar energy and the like, wherein the solar energy is considered as the safest and cleanest renewable energy source due to the characteristics of no pollution and inexhaustibility, so the development of low-cost solar energy technology is an important approach for solving the energy environmental problem. Quantum dot sensitized solar cells (QDSCs), as a class of photovoltaic devices that are simple to fabricate and inexpensive, are considered to be one of the most promising third-generation solar cells. The cell has simple structure and is generally composed of a photo-anode (TiO) 2 、SnO 2 ZnO, etc.), sensitizer (quantum dot, etc.), electrolyte (Sn) 2- /S 2- 、((CH 3 ) 4 N) 2 S/((CH 3 ) 4 N) 2 Sn, etc.), and the counter electrode, and the whole structure is in a sandwich shape.
As an important component of the solar cell, the electrolyte not only plays a role in transferring carriers, reducing photogenerated holes and realizing quantum dot regeneration, but also plays a role in oxidation-reduction potential and TiO 2 The difference in fermi levels of (a) determines the open circuit voltage of the cell, so the properties of the electrolyte directly affect the photovoltaic performance of the cell. In the current research of quantum dot sensitized solar cells, polysulfide aqueous solution is mostly adopted as electrolyte, but the defects of easy volatilization, easy leakage and the like of polysulfide aqueous solution cause great obstacles to the stability and practicability of quantum dot sensitized solar cells. The electrolyte is solidified through a certain technology, which is a new idea in the research of the electrolyte of the sensitized solar cell. In recent studies, the types of cured electrolytes can be broadly divided into two types, one being a polymer quasi-solid electrolyte cured in a gel state, and one being a solid electrolyte cured based on a molecular or hole conductor.
At present, methods of stirring solidification or heating stirring and cooling solidification are mostly adopted for solidifying the polysulfide aqueous solution electrolyte into the gel quasi-solid electrolyte, but the methods have the problems of uneven stirring, incomplete stirring and the like when the content of the solidifying agent is high, and even have the phenomenon of slow stirring speed when the consistency of the electrolyte is increased, and the phenomena have great influence on the photovoltaic performance of the battery.
Disclosure of Invention
The invention aims to provide a preparation method of a quasi-solid electrolyte for a quantum dot sensitized solar cell, which is characterized in that on the premise of ensuring that the photovoltaic performance of the quantum dot sensitized solar cell is not influenced, a past electrolyte curing method is innovated, an electrolyte and a curing agent are combined together by adopting a grinding technology, and a polysulfide electrolyte of the quantum dot sensitized solar cell is cured to form the quasi-solid electrolyte, so that the problems that the liquid electrolyte is easy to leak and difficult to store are solved, and the problems that the electrolyte and the curing agent are not uniformly mixed and not thorough due to the past stirring preparation process are solved.
The invention is realized by the following steps:
a preparation method of a quasi-solid electrolyte for a quantum dot sensitized solar cell comprises the following steps:
(1) Preparing polysulfide electrolyte: weighing appropriate amount of Na 2 S·9H 2 Adding deionized water into O and S powder and potassium chloride, stirring until the mixture is uniform, has no particles, is orange, is clear and transparent, and then carrying out ultrasonic decomposition.
(2) Weighing a certain amount of sodium carboxymethylcellulose (CMC-Na) and polyvinylpyrrolidone (PVP) for later use.
(3) Preparing a quasi-solid electrolyte: taking a small amount of sodium carboxymethylcellulose (CMC-Na) and polyvinylpyrrolidone (PVP) and putting into a mortar for uniformly mixing, then adding a small amount of prepared polysulfide electrolyte into the mortar for grinding, and continuously and gradually adding a small amount of polysulfide electrolyte, sodium carboxymethylcellulose (CMC-Na) and polyvinylpyrrolidone (PVP) during grinding until the three are completely and uniformly ground.
(4) The ground quasi-solid electrolyte is filled into a sample bottle and is placed in a shade place for sealed storage.
Further optimization, the step (1)In Na 2 S·9H 2 The mass ratio of O powder to S powder to potassium chloride is 8 2 S·9H 2 The mass ratio of O to deionized water is 1. The stirring process in the step comprises the following steps: stirring at 25 deg.C and rotor speed of 500r for 20min until the polysulfide electrolyte is orange, clear, transparent, uniform and particle-free. The ultrasonic decomposition treatment needs to control the temperature of the ultrasonic machine to be not higher than 40 ℃.
Further optimizing, in the step (2), the mass ratio of the sodium carboxymethyl cellulose (CMC-Na) to the polyvinylpyrrolidone (PVP) is 4.
Further optimizing, in the step (3), the grinding method is as follows: a small amount of sodium carboxymethylcellulose (CMC-Na) and polyvinylpyrrolidone (PVP) are gradually put into a mortar for grinding, and the mass of each time of putting is as follows: 0.4g of sodium carboxymethylcellulose (CMC-Na), 0.3g of polyvinylpyrrolidone (PVP) and 0.5mL of the prepared polysulfide electrolyte. During grinding, the uniform speed is required until the ground product is in a uniform yellow potato paste shape. If one reagent is used up, the rest reagents are ground continuously according to the proportion until the sodium carboxymethyl cellulose (CMC-Na), the polyvinylpyrrolidone (PVP) and the prepared polysulfide electrolyte are used up and the uniform mixing of the sodium carboxymethyl cellulose (CMC-Na), the polyvinylpyrrolidone (PVP) and the prepared polysulfide electrolyte is ensured.
In the conventional research on the dye-sensitized solar cell, the grinding technology is mostly used for preparing the counter electrode, and the preparation of the electrolyte and the quasi-solid electrolyte is basically realized by a stirring process. The invention develops a new method, firstly puts forward that the grinding process is connected with the quasi-solid electrolyte, changes the traditional electrolyte stirring, breaks through the limitation and has great innovation.
The quasi-solid electrolyte for the quantum dot sensitized solar cell is prepared by a grinding method, the method is simple, novel and unique to operate, and the quasi-solid polysulfide electrolyte is obtained by uniformly grinding the curing agent and the polysulfide electrolyte together. The grinding method adopted by the invention is innovative in the electrolyte preparation process, and the prepared quasi-solid electrolyte is convenient to store, solves the problem that the common polysulfide electrolyte is easy to leak, and also solves the problems of uneven and incomplete mixing of the curing agent and the electrolyte caused by stirring and curing. The preparation method is simple and efficient, ensures the same photovoltaic performance as that of the common polysulfide electrolyte, and has good application value.
Drawings
FIG. 1 is an electron microscope image of the surface morphology of the quasi-solid polysulfide electrolyte prepared by grinding process in example 1.
FIG. 2 is an electron microscope image of the surface morphology of the quasi-solid polysulfide electrolyte prepared by the stirring process in example 2.
Fig. 3 is a graph comparing J-V curves of the cells obtained by applying the electrolyte prepared by the milling process in example 1 and the stirring process in example 2 to the quantum dot sensitized solar cell.
Detailed Description
The following examples serve to illustrate the invention in further detail, but without restricting it in any way.
Example 1:
(1) Preparing polysulfide electrolyte: firstly 8gNa 2 S·9H 2 Dissolving O and 1g of S powder in 40mL of deionized water, setting the stirring temperature of a magnetic stirrer to be 25 ℃, setting the rotating speed of a rotor to be 500r, and controlling the stirring time to be 20min until the liquid is orange, clear, transparent, uniform and free of particles. Then, 1g of potassium chloride granules are weighed and put into the liquid and stirred for 20min continuously until the potassium chloride granules are completely dissolved. And finally, placing the prepared polysulfide electrolyte into an ultrasonic machine for ultrasonic decomposition for 10min, controlling the temperature of the ultrasonic machine not to be higher than 40 ℃ in the ultrasonic process, and placing the polysulfide electrolyte in a shade place for sealing and storing after ultrasonic treatment.
(2) Preparing a curing agent material: weighing 16g of sodium carboxymethylcellulose (CMC-Na) and 12g of polyvinylpyrrolidone (PVP) for standby.
(3) Preparing a quasi-solid polysulfide electrolyte: 0.4g of sodium carboxymethylcellulose (CMC-Na) and 0.3g of polyvinylpyrrolidone (PVP) are put into a mortar, and 0.5mL of the prepared polysulfide electrolyte is added dropwise after being uniformly mixed by a mortar rod and ground by a grinding rod. The grinding speed is controlled to be uniform until the curing agent and the polysulfide electrolyte are fully mixed, and the ground shape is a yellow potato mash with uniform texture. And then, continuously adding the curing agent and the polysulfide electrolyte into the mortar according to the proportion for grinding, and repeating the steps for a few times until the grinding is finished completely (in order to ensure the optimal proportion, the weighed two curing agents and the prepared polysulfide electrolyte are used completely, and if the curing agents and the prepared polysulfide electrolyte are used up, the rest of the reagents are continuously ground according to the proportion until the sodium carboxymethylcellulose (CMC-Na) and the polyvinylpyrrolidone (PVP) are used up, and the prepared polysulfide electrolyte is uniformly mixed, which is the same as the above step.
(4) And filling the ground quasi-solid polysulfide electrolyte into a sample bottle, and placing the sample bottle in a shade place for closed storage.
(5) And (3) testing the efficiency of the battery: the quasi-solid electrolyte is coated on a photo-anode adsorbing quantum dots in a blade mode, the quantum dots are completely covered and soaked by the electrolyte in the blade coating process, and then the photo-anode (the photo-anode coated with the quasi-solid polysulfide electrolyte in a blade mode) and an counter electrode (a polished copper sheet) are assembled together to form the complete quantum dot sensitized solar cell. Through the test of simulating standard sunlight, the quasi-solid polysulfide electrolyte prepared by the method is applied to a quantum dot sensitized solar cell, and the photoelectric conversion efficiency of the solar cell is as follows: 6.67 percent.
Example 2:
(1) Preparing polysulfide electrolyte: firstly 8gNa 2 S·9H 2 Dissolving O,1g of S powder in 40mL of deionized water, setting the stirring temperature of a magnetic stirrer to be 25 ℃, setting the rotating speed of a rotor to be 500r, and controlling the stirring time to be 20min until the liquid is orange, clear, transparent, uniform and free of particles. Then, 1g of potassium chloride granules are weighed and put into the liquid and stirred for 20min continuously until the potassium chloride granules are completely dissolved. And finally, placing the prepared polysulfide electrolyte into an ultrasonic machine for ultrasonic decomposition for 10min, controlling the temperature of the ultrasonic machine not to be higher than 40 ℃ in the ultrasonic process, and placing the polysulfide electrolyte in a shade place for sealing and storing after ultrasonic treatment.
(2) Preparing a curing agent material: weighing 16g of sodium carboxymethylcellulose (CMC-Na) and 12g of polyvinylpyrrolidone (PVP) for later use.
(3) Preparing a quasi-solid polysulfide electrolyte: firstly, 12g of polyvinylpyrrolidone (PVP) is added into the prepared polysulfide electrolyte, and the polysulfide electrolyte is stirred by a magnetic stirrer, the stirring temperature of the magnetic stirrer is set to be 25 ℃, the rotating speed of a rotor is set to be 500r, and the stirring time is controlled to be 20min until the liquid is orange, clear, transparent, uniform and free of particles. Then, 16g of sodium carboxymethylcellulose (CMC-Na) is added into the mixture, and the mixture is stirred by a magnetic stirrer, wherein the stirring temperature of the magnetic stirrer is set to be 25 ℃, the rotating speed of a rotor is set to be 300r, and the stirring time is controlled to be 20min until the gel is formed. The stirring state is observed all the time, if the speed of the stirring rotor is reduced or even does not rotate due to the increase of the consistency of the electrolyte, the speed of the magnetic stirrer and the position of the bottle are adjusted in time to ensure the uniform mixing of the sodium carboxymethylcellulose and the electrolyte. And finally, placing the prepared quasi-solid polysulfide electrolyte into an ultrasonic machine for ultrasonic decomposition for 10min, and controlling the temperature of the ultrasonic machine not to be higher than 40 ℃ in the ultrasonic process.
(4) And filling the prepared quasi-solid polysulfide electrolyte into a sample bottle, and hermetically storing the sample bottle in a shade place.
(5) And (3) testing the efficiency of the battery: the quasi-solid electrolyte is coated on a photo-anode adsorbing quantum dots in a scraping way, the quantum dots are ensured to be completely covered and soaked by the electrolyte in the scraping way, and then the photo-anode coated with the quasi-solid polysulfide electrolyte and a counter electrode (polished copper sheet) are assembled together to construct a complete quantum dot sensitized solar cell. Through the test of simulating standard sunlight, the quasi-solid polysulfide electrolyte prepared by the method is applied to a quantum dot sensitized solar cell, and the photoelectric conversion efficiency of the solar cell is as follows: 5.31 percent.
SEM tests were performed on the quasi-solid polysulfide electrolytes prepared in examples 1 and 2, and the results are shown in fig. 1 and 2, respectively. The quasi-solid polysulfide electrolytes prepared in example 1 and example 2 were used in quantum dot sensitized solar cells, and the J-V curves of the cells are shown in fig. 3.
As can be seen from the electron microscope images in fig. 1 and fig. 2, the quasi-solid electrolyte prepared by the stirring process has fewer surface voids and smoother surface, and forms a thin film layer, which may be caused by that the mixed surface of the electrolyte and the CMC-Na is hermetically distributed due to the stirring, so that interparticle pores cannot be clearly distinguished, and the diffusion of the electrolyte is not facilitated. The electrolyte prepared by the grinding process has larger gaps on the surface, and can promote the permeation of the electrolyte, thereby increasing the rapid diffusion of redox couples, and being beneficial to the exertion of the function of the electrolyte and the normal work of the battery.
As can be seen from FIG. 3, in the case of only changing the curing method without changing the specification and content of the used reagents, and comparing with the stirring process, the quasi-solid polysulfide electrolyte prepared by the innovative grinding process of the invention is applied to the quantum dot sensitized solar cell, and the photovoltaic performance of the cell is greatly improved.
Example 3:
(1) Preparing a polysulfide electrolyte: firstly 8gNa 2 S·9H 2 Dissolving O and 1g of S powder in 40mL of deionized water, setting the stirring temperature of a magnetic stirrer to be 25 ℃, setting the rotating speed of a rotor to be 500r, and controlling the stirring time to be 20min until the liquid is orange, clear, uniform and free of particles. Then, 1g of potassium chloride granules was weighed into the above liquid and stirred for another 20min until the potassium chloride granules were completely dissolved. And finally, placing the prepared polysulfide electrolyte into an ultrasonic machine for ultrasonic decomposition for 10min, controlling the temperature of the ultrasonic machine not to be higher than 40 ℃ in the ultrasonic process, and placing the polysulfide electrolyte in a shade place for sealing and storing after ultrasonic treatment.
(2) Preparing a curing agent material: 12g of sodium carboxymethylcellulose (CMC-Na) and 9g of polyvinylpyrrolidone (PVP) are weighed for standby.
(3) Preparing a quasi-solid polysulfide electrolyte: 0.4g of sodium carboxymethylcellulose (CMC-Na) and 0.3g of polyvinylpyrrolidone (PVP) are put into a mortar, and 0.5mL of the prepared polysulfide electrolyte is added dropwise after being uniformly mixed by a mortar rod and ground by a grinding rod. The grinding speed is controlled to be uniform until the curing agent and the polysulfide electrolyte are fully mixed, and the ground shape is a yellow potato mash with uniform texture. And then, continuously adding the curing agent and the polysulfide electrolyte into the mortar according to the proportion for grinding, and repeating the steps for a few times until the grinding is finished.
(4) And filling the ground quasi-solid polysulfide electrolyte into a sample bottle, and placing the sample bottle in a shade place for closed storage.
(5) And (3) testing the efficiency of the battery: and scraping the quasi-solid electrolyte on a photo-anode adsorbed with the quantum dots, ensuring that the quantum dots are completely covered and infiltrated by the electrolyte during scraping, and then assembling the photo-anode (coated quasi-solid polysulfide electrolyte) and a counter electrode (copper sheet) together to construct a complete quantum dot sensitized solar cell. Through the test of simulating standard sunlight, the quasi-solid polysulfide electrolyte prepared by the method is applied to a quantum dot sensitized solar cell, and the photoelectric conversion efficiency of the solar cell is as follows: 5.87 percent.
Example 4:
(1) Preparing a polysulfide electrolyte: firstly 8gNa 2 S·9H 2 Dissolving O and 1g of S powder in 40mL of deionized water, setting the stirring temperature of a magnetic stirrer to be 25 ℃, setting the rotating speed of a rotor to be 500r, and controlling the stirring time to be 20min until the liquid is orange, clear, uniform and free of particles. Then, 1g of potassium chloride granules was weighed into the above liquid and stirred for another 20min until the potassium chloride granules were completely dissolved. And finally, placing the prepared polysulfide electrolyte into an ultrasonic machine for ultrasonic decomposition for 10min, controlling the temperature of the ultrasonic machine not to be higher than 40 ℃ in the ultrasonic process, and placing the polysulfide electrolyte in a shade place for sealing and storing after ultrasonic treatment.
(2) Preparing a curing agent material: 20g of sodium carboxymethylcellulose (CMC-Na) and 15g of polyvinylpyrrolidone (PVP) are weighed for standby.
(3) Preparing a quasi-solid polysulfide electrolyte: 0.4g of sodium carboxymethylcellulose (CMC-Na) and 0.3g of polyvinylpyrrolidone (PVP) are put into a mortar, and 0.5mL of the prepared polysulfide electrolyte is added dropwise after being uniformly mixed by a mortar rod and ground by a grinding rod. The grinding speed is controlled to be uniform until the curing agent and the polysulfide electrolyte are fully mixed, and the ground form is a yellow potato mash with uniform texture. And then, continuously adding the curing agent and the polysulfide electrolyte into the mortar according to the proportion for grinding, and repeating the steps for a few times until the grinding is finished.
(4) And filling the ground quasi-solid polysulfide electrolyte into a sample bottle, and placing the sample bottle in a shade place for closed storage.
(5) And (3) testing the efficiency of the battery: the quasi-solid electrolyte is coated on a photo-anode adsorbing quantum dots in a blade mode, the quantum dots are completely covered and soaked by the electrolyte in the blade coating process, and then the photo-anode (coated quasi-solid polysulfide electrolyte) and a counter electrode (copper sheet) are assembled together to form the complete quantum dot sensitized solar cell. Through the test of simulating standard sunlight, the quasi-solid polysulfide electrolyte prepared by the method is applied to a quantum dot sensitized solar cell, and the photoelectric conversion efficiency of the solar cell is as follows: 6.01 percent.
By comparing example 1 with examples 3 and 4, on the premise that the quasi-solid electrolyte is prepared by using a grinding method, the ratio of the polysulfide electrolyte and the curing agent used in example 1 is the optimal ratio, and the quasi-solid polysulfide electrolyte prepared by using the ratio in example 1 is applied to a quantum dot sensitized solar cell, and the cell can show the best photovoltaic performance.

Claims (5)

1. A preparation method of a quasi-solid electrolyte for a quantum dot sensitized solar cell is characterized by comprising the following steps:
a. preparing a polysulfide electrolyte: weighing Na 2 S·9H 2 Adding deionized water into O and S powder and potassium chloride, stirring until the mixture is uniform, free of particles, orange, clear and transparent, and then performing ultrasonic decomposition;
b. weighing curing agents of sodium carboxymethylcellulose and polyvinylpyrrolidone for later use;
c. preparing a quasi-solid electrolyte: sequentially taking the sodium carboxymethylcellulose, the polyvinylpyrrolidone and the polysulfide electrolyte according to a set proportion, mixing and grinding in a mortar until the sodium carboxymethylcellulose, the polyvinylpyrrolidone and the polysulfide electrolyte are completely and uniformly ground;
d. the ground quasi-solid electrolyte is filled into a sample bottle and is placed in a shade place for sealed storage.
2. The quasi-solid electrolyte for a quantum dot sensitized solar cell according to claim 1The process of (a), wherein in the step (a), na 2 S·9H 2 The mass ratio of O powder to S powder to potassium chloride is 8; na (Na) 2 S·9H 2 The mass ratio of O to deionized water is 1.
3. The method for preparing the quasi-solid electrolyte for the quantum dot sensitized solar cell according to claim 1, wherein in the step a, the stirring process comprises: stirring at 25 deg.C and rotor speed of 500r for 20min until the polysulfide electrolyte is orange, clear, transparent, uniform and particle-free; the ultrasonic decomposition treatment needs to control the temperature of the ultrasonic machine not to be higher than 40 ℃.
4. The method of claim 1, wherein in the step b, the mass ratio of the sodium carboxymethylcellulose to the polyvinylpyrrolidone is 4.
5. The method of claim 1, wherein the amounts of the sodium carboxymethyl cellulose, the polyvinylpyrrolidone and the polysulfide electrolyte added in step c are 0.4g, 0.3g and 0.5mL per milling, respectively.
CN202210994863.XA 2022-08-18 2022-08-18 Preparation method of quasi-solid electrolyte for quantum dot sensitized solar cell Active CN115512972B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN202210994863.XA CN115512972B (en) 2022-08-18 2022-08-18 Preparation method of quasi-solid electrolyte for quantum dot sensitized solar cell

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN202210994863.XA CN115512972B (en) 2022-08-18 2022-08-18 Preparation method of quasi-solid electrolyte for quantum dot sensitized solar cell

Publications (2)

Publication Number Publication Date
CN115512972A true CN115512972A (en) 2022-12-23
CN115512972B CN115512972B (en) 2023-11-03

Family

ID=84502888

Family Applications (1)

Application Number Title Priority Date Filing Date
CN202210994863.XA Active CN115512972B (en) 2022-08-18 2022-08-18 Preparation method of quasi-solid electrolyte for quantum dot sensitized solar cell

Country Status (1)

Country Link
CN (1) CN115512972B (en)

Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1868582A (en) * 2006-06-02 2006-11-29 安徽大学 Nanometer titanium dioxide/selenium dioxide composition and its prepn. method
CN101728082A (en) * 2009-11-20 2010-06-09 大连工业大学 Method for preparing composite electrode of flexible dye-sensitized solar cell
CN103247444A (en) * 2013-05-07 2013-08-14 常州大学 Quantum dot and dye co-sensitization solar battery and preparation method thereof
CN105244169A (en) * 2015-10-21 2016-01-13 景德镇陶瓷学院 Quasi-solid-state electrolyte for dye sensitized solar cell and preparation method of quasi-solid-state electrolyte
CN106328381A (en) * 2016-11-23 2017-01-11 陕西理工学院 All-solid-state quantum dot sensitized solar cell and preparation method thereof
CN107039187A (en) * 2017-04-17 2017-08-11 中南大学 A kind of dystopy adsorbs the preparation method of the quantum dot sensitized solar cell of silver selenide
CN109616328A (en) * 2018-12-05 2019-04-12 河北工业大学 A kind of preparation method of the quantum dot sensitized solar battery of surface passivation CdSeTe
CN109841418A (en) * 2017-11-27 2019-06-04 李艳 It is sensitized the preparation of quantum dot solar cell light anode altogether
CN112467194A (en) * 2020-12-09 2021-03-09 中国科学院上海硅酸盐研究所 Organic-inorganic composite quasi-solid electrolyte and quasi-solid lithium battery

Patent Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1868582A (en) * 2006-06-02 2006-11-29 安徽大学 Nanometer titanium dioxide/selenium dioxide composition and its prepn. method
CN101728082A (en) * 2009-11-20 2010-06-09 大连工业大学 Method for preparing composite electrode of flexible dye-sensitized solar cell
CN103247444A (en) * 2013-05-07 2013-08-14 常州大学 Quantum dot and dye co-sensitization solar battery and preparation method thereof
CN105244169A (en) * 2015-10-21 2016-01-13 景德镇陶瓷学院 Quasi-solid-state electrolyte for dye sensitized solar cell and preparation method of quasi-solid-state electrolyte
CN106328381A (en) * 2016-11-23 2017-01-11 陕西理工学院 All-solid-state quantum dot sensitized solar cell and preparation method thereof
CN107039187A (en) * 2017-04-17 2017-08-11 中南大学 A kind of dystopy adsorbs the preparation method of the quantum dot sensitized solar cell of silver selenide
CN109841418A (en) * 2017-11-27 2019-06-04 李艳 It is sensitized the preparation of quantum dot solar cell light anode altogether
CN109616328A (en) * 2018-12-05 2019-04-12 河北工业大学 A kind of preparation method of the quantum dot sensitized solar battery of surface passivation CdSeTe
CN112467194A (en) * 2020-12-09 2021-03-09 中国科学院上海硅酸盐研究所 Organic-inorganic composite quasi-solid electrolyte and quasi-solid lithium battery

Also Published As

Publication number Publication date
CN115512972B (en) 2023-11-03

Similar Documents

Publication Publication Date Title
Chen et al. A scalable electrodeposition route to the low-cost, versatile and controllable fabrication of perovskite solar cells
CN101728082B (en) Method for preparing composite electrode of flexible dye-sensitized solar cell
CN104465113A (en) Nitrogen-doped graphene counter electrode preparing method and application of nitrogen-doped graphene counter electrode in dye-sensitized solar cell
CN106128772B (en) A kind of preparation method of vulcanized lead quantum dot photovoltaic battery
CN107359372A (en) A kind of aqueous electrolyte and Water based metal ion battery
CN112786790A (en) Perovskite solar cell, interface modification layer thereof and preparation method of modification layer
CN103594249B (en) A kind of graphene oxide-nano-graphite flour complexes is to the preparations and applicatio of electrode
CN101996771B (en) Tin dioxide ceramic electrode, preparation method thereof and dye sensitized solar cell
CN110676073A (en) Electrolyte, enhanced all-solid-state flexible supercapacitor based on electrolyte and preparation method of enhanced all-solid-state flexible supercapacitor
CN101572190B (en) Method for preparing TiO2 slurry of organic carrier system
CN115512972B (en) Preparation method of quasi-solid electrolyte for quantum dot sensitized solar cell
CN114538788B (en) Preparation method of layered double hydroxide electrochromic energy storage film
CN103400941B (en) Based on the organic solar batteries and preparation method thereof of heteropoly acid anode modification layer
CN103295793B (en) The purposes of polyvinyl butyral, dye-sensitized solar cells quasi-solid electrolyte film and preparation method thereof
CN106847518B (en) A kind of dye-sensitized solar cell anode and preparation method thereof
CN114400263B (en) Preparation method and application of substrate-supported bismuth halide/bismuth sulfide nanosheet heterojunction device
CN110265650A (en) A kind of lithium ion battery nanoporous composite negative pole material and preparation method thereof
CN109712814A (en) A kind of FeCo of efficient stable2S4The preparation method and application of conductive film
CN109326445B (en) Nano composite counter electrode for quantum dot sensitized solar cell and preparation method
CN106803460A (en) A kind of CuS for quantum dot sensitized solar cell is to electrode and preparation method thereof
CN107068409B (en) A kind of dye-sensitized solar cells comprising optimizing structure optoelectronic pole
CN100472816C (en) Soft-base solid pigment sensitive film solar cell and its prepn. method
CN104576064A (en) Method for manufacturing ZnO/SnO2 compound light anode of dye-sensitized solar cell
CN109279626A (en) Nano-sheet kalium ion battery positive electrode and preparation method thereof and kalium ion battery
CN104332319A (en) Method for manufacturing dye-sensitized solar cell through full screen printing

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