CN110003450B - Interface material: zwitterionic conjugated polyelectrolytes with amino acid groups - Google Patents

Interface material: zwitterionic conjugated polyelectrolytes with amino acid groups Download PDF

Info

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
Application number
CN201910273657.8A
Other languages
Chinese (zh)
Other versions
CN110003450A (en
Inventor
不公告发明人
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.)
Nanjing Hesong Material Technology Co., Ltd
Original Assignee
Nanjing Hesong Material Technology Co Ltd
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 Nanjing Hesong Material Technology Co Ltd filed Critical Nanjing Hesong Material Technology Co Ltd
Priority to CN201910273657.8A priority Critical patent/CN110003450B/en
Publication of CN110003450A publication Critical patent/CN110003450A/en
Application granted granted Critical
Publication of CN110003450B publication Critical patent/CN110003450B/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Images

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G61/00Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
    • C08G61/12Macromolecular compounds containing atoms other than carbon in the main chain of the macromolecule
    • C08G61/122Macromolecular compounds containing atoms other than carbon in the main chain of the macromolecule derived from five- or six-membered heterocyclic compounds, other than imides
    • C08G61/123Macromolecular 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
    • C08G61/126Macromolecular 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
    • HELECTRICITY
    • H10SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10KORGANIC ELECTRIC SOLID-STATE DEVICES
    • H10K30/00Organic devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation
    • H10K30/10Organic devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation comprising heterojunctions between organic semiconductors and inorganic semiconductors
    • HELECTRICITY
    • H10SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10KORGANIC ELECTRIC SOLID-STATE DEVICES
    • H10K30/00Organic devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation
    • H10K30/80Constructional details
    • HELECTRICITY
    • H10SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10KORGANIC ELECTRIC SOLID-STATE DEVICES
    • H10K85/00Organic materials used in the body or electrodes of devices covered by this subclass
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G2261/00Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
    • C08G2261/10Definition of the polymer structure
    • C08G2261/11Homopolymers
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G2261/00Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
    • C08G2261/10Definition of the polymer structure
    • C08G2261/14Side-groups
    • C08G2261/143Side-chains containing nitrogen
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G2261/00Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
    • C08G2261/10Definition of the polymer structure
    • C08G2261/18Definition of the polymer structure conjugated
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G2261/00Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
    • C08G2261/30Monomer units or repeat units incorporating structural elements in the main chain
    • C08G2261/32Monomer units or repeat units incorporating structural elements in the main chain incorporating heteroaromatic structural elements in the main chain
    • C08G2261/322Monomer units or repeat units incorporating structural elements in the main chain incorporating heteroaromatic structural elements in the main chain non-condensed
    • C08G2261/3223Monomer 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
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02EREDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E10/00Energy generation through renewable energy sources
    • Y02E10/50Photovoltaic [PV] energy
    • Y02E10/549Organic PV cells

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

Interface material: zwitterionic conjugated polyelectrolytes with amino acid groups
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,
Figure 100002_DEST_PATH_IMAGE001
wherein y =1-8
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.
Figure DEST_PATH_IMAGE002
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)

1. A zwitter-ion conjugated polyelectrolyte with amino acid groups is used for interface modification of an electron transport layer in a perovskite solar cell, and the structural formula of the zwitter-ion conjugated polyelectrolyte is as follows:
Figure DEST_PATH_IMAGE001
wherein y = 1-8.
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.
CN201910273657.8A 2019-04-06 2019-04-06 Interface material: zwitterionic conjugated polyelectrolytes with amino acid groups Active CN110003450B (en)

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)

* Cited by examiner, † Cited by third party
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)

* Cited by examiner, † Cited by third party
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

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