CN110003450B - Interface material: zwitterionic conjugated polyelectrolytes with amino acid groups - Google Patents
Interface material: zwitterionic conjugated polyelectrolytes with amino acid groups Download PDFInfo
- Publication number
- CN110003450B CN110003450B CN201910273657.8A CN201910273657A CN110003450B CN 110003450 B CN110003450 B CN 110003450B CN 201910273657 A CN201910273657 A CN 201910273657A CN 110003450 B CN110003450 B CN 110003450B
- Authority
- CN
- China
- Prior art keywords
- conjugated polyelectrolyte
- solar cell
- amino acid
- acid groups
- spin coating
- 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
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G61/00—Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
- C08G61/12—Macromolecular compounds containing atoms other than carbon in the main chain of the macromolecule
- C08G61/122—Macromolecular compounds containing atoms other than carbon in the main chain of the macromolecule derived from five- or six-membered heterocyclic compounds, other than imides
- C08G61/123—Macromolecular compounds containing atoms other than carbon in the main chain of the macromolecule derived from five- or six-membered heterocyclic compounds, other than imides derived from five-membered heterocyclic compounds
- C08G61/126—Macromolecular compounds containing atoms other than carbon in the main chain of the macromolecule derived from five- or six-membered heterocyclic compounds, other than imides derived from five-membered heterocyclic compounds with a five-membered ring containing one sulfur atom in the ring
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K30/00—Organic devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation
- H10K30/10—Organic devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation comprising heterojunctions between organic semiconductors and inorganic semiconductors
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K30/00—Organic devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation
- H10K30/80—Constructional details
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K85/00—Organic materials used in the body or electrodes of devices covered by this subclass
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G2261/00—Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
- C08G2261/10—Definition of the polymer structure
- C08G2261/11—Homopolymers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G2261/00—Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
- C08G2261/10—Definition of the polymer structure
- C08G2261/14—Side-groups
- C08G2261/143—Side-chains containing nitrogen
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G2261/00—Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
- C08G2261/10—Definition of the polymer structure
- C08G2261/18—Definition of the polymer structure conjugated
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G2261/00—Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
- C08G2261/30—Monomer units or repeat units incorporating structural elements in the main chain
- C08G2261/32—Monomer units or repeat units incorporating structural elements in the main chain incorporating heteroaromatic structural elements in the main chain
- C08G2261/322—Monomer units or repeat units incorporating structural elements in the main chain incorporating heteroaromatic structural elements in the main chain non-condensed
- C08G2261/3223—Monomer units or repeat units incorporating structural elements in the main chain incorporating heteroaromatic structural elements in the main chain non-condensed containing one or more sulfur atoms as the only heteroatom, e.g. thiophene
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E10/00—Energy generation through renewable energy sources
- Y02E10/50—Photovoltaic [PV] energy
- Y02E10/549—Organic PV cells
Landscapes
- Chemical & Material Sciences (AREA)
- Physics & Mathematics (AREA)
- Electromagnetism (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Photovoltaic Devices (AREA)
Abstract
The invention aims to provide a zwitter-ion conjugated polyelectrolyte with amino acid groups, which has water/alcohol solubility and specific interface optimization performance; the material is used as an interface material for modifying an electron transport layer in an n-i-p perovskite solar cell; the perovskite solar cell and the organic solar cell have potential and wide application prospect in the perovskite solar cell, the organic solar cell and the organic light emitting diode.
Description
Technical Field
The invention relates to an application of zwitter-ion conjugated polyelectrolyte with amino acid group as an interface material in an n-i-p perovskite solar cell.
Background
The perovskite solar cell is developed very rapidly, and is judged as one of ten international technological advances by Science in 2013, so that the perovskite solar cell becomes one of research hotspots of a novel solar cell. The perovskite solar cell is composed of an electrode, an electron transport layer, a hole transport layer and a light active layer, and the performance of the perovskite solar cell depends on the structure of a device, the interface performance between a material and a functional layer; the interface material can modify the functional layer through interface engineering, enhance the transmission and collection of charges, and improve the interface contact among different materials with different properties, thereby realizing the solar cell with high stability and high photoelectric conversion efficiency.
Disclosure of Invention
The invention aims to provide application of zwitter-ion conjugated polyelectrolyte with amino acid group as an interface material in an n-i-p perovskite solar cell.
The invention is characterized in that the structural general formula of the zwitterionic conjugated polyelectrolyte with amino acid groups is shown as the following formula,
The invention also features the use of a zwitterionic conjugated polyelectrolyte with amino acid groups in n-i-p perovskite solar cells.
Drawings
The above features and advantages of the present invention will be more clearly understood by reference to the following drawings and detailed description, in which:
AFM topography for the POWT film of material of FIG. 1;
FIG. 2 perovskite solar cell Current Density/Voltage ((R))J sc /V oc ) Graph is shown.
Detailed description of the preferred embodiments
The implementation case is as follows:
in the following, preferred embodiments of the present invention are described in detail so that the advantages and features of the present invention can be more easily understood by those skilled in the art, taking polymer POWT (y = 1) as an example.
Performance characterization of the POWT material:
POWT can be dissolved in polar solvent, and the solution can be formed into film by spin coating; the film has good and uniform quality, the surface roughness is 2.33 nm (figure I), and the preparation of the perovskite film with good uniformity is facilitated.
Preparation and characterization of perovskite solar cells:
(1) the ITO substrate of 1.5 cm x 1.5 cm is subjected to ultrasonic treatment twice in deionized water, then is subjected to ultrasonic treatment once in acetone and isopropanol respectively, is dried by a nitrogen gun, and is placed in an ultraviolet-ozone instrument for treatment for 15 min.
(2) Cell ITO/SnO2/POWT/CH3NH3PbI3Preparation of/Spiro-OMeTAD/Au:
firstly, preparing electronic transmission material SnO on ITO substrate by using spin coating method2Annealing the film for 30min at 150 ℃; then spin coating a methanol/water solution of a zwitterionic conjugated polyelectrolyte to SnO2Annealing the film at 100 deg.C for 20 min; then the prepared PbI is put into2Spin coating a mixed solution of MAI and DMSO in DMF to ITO/SnO2Annealing the surface of the zwitter ion conjugated polyelectrolyte at 130 ℃ for 10 min; spin coating a cavity transport material Spiro-OMeTAD film; and finally, obtaining the Au electrode by using an evaporation method.
(3) And (3) testing the battery performance:
devices were performance tested using Keithley 2400: under simulated AM 1.5G sunlight irradiation conditions (light intensity of 100 mW/cm)2) A photocurrent density/voltage curve was obtained with a scan rate of 50 mV/S.
The ITO/SnO of the battery2/POWT/CH3NH3PbI3Data were collected after voltage forward and reverse sweeps of/Spiro-OMeTAD/Au.Obtaining open circuit voltage under normal scan condition (V oc ) 1.01V, and a short-circuit current density ofJ sc ) Is 25.63 mA cm-2The Fill Factor (FF) was 62.98% and the photoelectric conversion efficiency was 16.24%.
Claims (2)
2. The use of the zwitterion conjugated polyelectrolyte with amino acid groups according to claim 1 for the interfacial modification of electron transport layers in perovskite solar cells, characterized in that: the method for modifying the conjugated polyelectrolyte interface material comprises the following steps:
preparation of electronic transmission material SnO on ITO substrate by spin coating method2Annealing the film for 30min at 150 ℃; then spin coating a methanol/water solution of a zwitterionic conjugated polyelectrolyte to SnO2Annealing the film at 100 deg.C for 20 min; then the prepared PbI is put into2Spin coating a mixed solution of MAI and DMSO in DMF to ITO/SnO2Annealing the surface of the zwitter ion conjugated polyelectrolyte at 130 ℃ for 10 min; spin coating a cavity transport material Spiro-OMeTAD film; and finally, obtaining the Au electrode by using an evaporation method.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201910273657.8A CN110003450B (en) | 2019-04-06 | 2019-04-06 | Interface material: zwitterionic conjugated polyelectrolytes with amino acid groups |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201910273657.8A CN110003450B (en) | 2019-04-06 | 2019-04-06 | Interface material: zwitterionic conjugated polyelectrolytes with amino acid groups |
Publications (2)
Publication Number | Publication Date |
---|---|
CN110003450A CN110003450A (en) | 2019-07-12 |
CN110003450B true CN110003450B (en) | 2020-11-06 |
Family
ID=67170124
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN201910273657.8A Active CN110003450B (en) | 2019-04-06 | 2019-04-06 | Interface material: zwitterionic conjugated polyelectrolytes with amino acid groups |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN110003450B (en) |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN109942800B (en) * | 2019-04-08 | 2020-10-20 | 南京和颂材料科技有限公司 | Zwitterion conjugated polyelectrolyte interface material with amino acid group |
CN110408008B (en) * | 2019-07-04 | 2022-03-18 | 南京工业大学 | Application of zwitterion conjugated polyelectrolyte with amino acid group and having hole transport performance |
CN110504362B (en) * | 2019-07-17 | 2023-06-16 | 浙江浙能技术研究院有限公司 | SnO (tin oxide) 2 Modification method of electron selective transport layer |
CN111564559B (en) * | 2020-04-09 | 2022-11-08 | 宁波材料所杭州湾研究院 | Electron transport layer, preparation method thereof, perovskite cell structure and solar cell |
Family Cites Families (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
SE0400783D0 (en) * | 2004-03-24 | 2004-03-24 | Peter Aasberg | Pattern method for biosensor applications |
JP2013163793A (en) * | 2012-02-13 | 2013-08-22 | Tosoh Corp | Amino acid derivative for conductive monomer |
CN103951813B (en) * | 2014-03-31 | 2016-08-17 | 南京邮电大学 | 9-aryl replaces fluorenyl conjugated polyelectrolytes and its preparation method and application |
CN104804176A (en) * | 2015-05-08 | 2015-07-29 | 东南大学 | Full-conjugated block polyelectrolyte and preparation method thereof |
CN105237745A (en) * | 2015-10-13 | 2016-01-13 | 华南理工大学 | Quaternary phosphonium salt group-containing conjugated polyelectrolyte and its use in organic photoelectric device |
CN108470852A (en) * | 2018-04-10 | 2018-08-31 | 南京邮电大学 | A kind of preparation method of modifying interface perovskite solar cell |
-
2019
- 2019-04-06 CN CN201910273657.8A patent/CN110003450B/en active Active
Also Published As
Publication number | Publication date |
---|---|
CN110003450A (en) | 2019-07-12 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN110003450B (en) | Interface material: zwitterionic conjugated polyelectrolytes with amino acid groups | |
CN107394047B (en) | Application of alcohol-soluble fullerene derivative in perovskite solar cell | |
CN109942800B (en) | Zwitterion conjugated polyelectrolyte interface material with amino acid group | |
CN111883659B (en) | Efficient ternary organic solar cell prepared based on gradual deposition method | |
CN105470399A (en) | Perovskite solar cell based on undoped organic hole transport layer and preparation method | |
WO2024066584A1 (en) | Perovskite cell, photovoltaic module, photovoltaic power generation system, and electric device | |
CN103346260A (en) | Organic-inorganic hybrid solar cell with passivated organic thin film and preparation method thereof | |
US9040318B2 (en) | Lamination as a modular approach for building organic photosensitive devices | |
CN112018242A (en) | Perovskite solar cell and preparation method thereof | |
CN106410037A (en) | Small organic molecule donor material based double-junction solar cell device and preparation method thereof | |
CN113644202B (en) | Organic solar cell prepared by spontaneous orientation film forming method and preparation method thereof | |
CN110649165A (en) | Perovskite battery with tetraphenylbiphenyldiamine derivative as hole transport material | |
CN113097388B (en) | Perovskite battery based on composite electron transport layer and preparation method thereof | |
CN113363389B (en) | Method for modifying p/i interface of perovskite solar cell | |
CN111100262A (en) | Electron transport material for perovskite solar cell | |
CN106410038B (en) | Application of naphthalene tetracarboxylic dianhydride derivative in inverted perovskite solar cell | |
CN106058056A (en) | Active layer of organic solar cell and preparation method of active layer | |
Song et al. | Spatially resolved characterization of solution processed perovskite solar cells using the lbic technique | |
KR100959760B1 (en) | Photovoltaic cell and method of manufacturing the same | |
CN110190192B (en) | Preparation method of trans-organic-inorganic hybrid perovskite solar cell | |
CN111653669A (en) | Small-molecule organic solar cell and preparation method thereof | |
CN110429183A (en) | A kind of heat-staple perovskite solar cell | |
CN113571643B (en) | Novel perovskite solar cell with organic hole transport layer and preparation method thereof | |
CN112952004B (en) | Organic photovoltaic device based on mixed solvent active layer and preparation method thereof | |
US11888443B2 (en) | Photo-charging storage device |
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 | ||
TA01 | Transfer of patent application right |
Effective date of registration: 20200929 Address after: Room 173, building a, 606 ningliu Road, Changlu street, Jiangbei new district, Nanjing, Jiangsu Province Applicant after: Nanjing Hesong Material Technology Co., Ltd Address before: 215200, Pang Yang Road 8, Wujiang economic and Technological Development Zone, Suzhou, Jiangsu Applicant before: SUZHOU HESONG BIOCHEMISTRY TECHNOLOGY Co.,Ltd. |
|
TA01 | Transfer of patent application right | ||
GR01 | Patent grant | ||
GR01 | Patent grant |