Looking for breakthrough ideas for innovation challenges? Try Patsnap Eureka!

A kind of preparation method and application of d-a type fluoroboron dipyrrole conjugated polymer

A type of fluoroboron dipyrrole, conjugated polymer technology, used in the field of solar cells, can solve the problems of disordered structure, low carrier mobility, poor durability, etc., to enhance the transfer of electrons and holes, and broaden the spectrum. Absorb and increase the effect of diffusion distance

Active Publication Date: 2021-08-31
NANCHANG HANGKONG UNIVERSITY
View PDF2 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0004] To sum up, the problems existing in the prior art are: the existing inorganic solar cells have complex processes, high manufacturing costs, high energy consumption and easy to cause environmental pollution.
Difficulty in solving the above technical problems: At present, the bottleneck restricting the development of organic solar cells lies in the low photoelectric conversion efficiency. At the same time, problems such as low carrier mobility, disordered structure, poor durability, and short life also affect the promotion of organic solar cells.

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • A kind of preparation method and application of d-a type fluoroboron dipyrrole conjugated polymer
  • A kind of preparation method and application of d-a type fluoroboron dipyrrole conjugated polymer
  • A kind of preparation method and application of d-a type fluoroboron dipyrrole conjugated polymer

Examples

Experimental program
Comparison scheme
Effect test

preparation example Construction

[0044] The first aspect of the present invention provides a method for preparing a D-A type fluoroboron dipyrrole conjugated polymer, such as figure 1 shown, including the following steps:

[0045] S101: Preparation of reaction raw materials and reaction conditions; the reaction raw materials are fluoroboron dipyrrole compounds (structural formulas are shown in formula I and formula II), electron-donating monomers, and catalysts;

[0046]S102: In an organic solvent system, under the protection of an inert gas, conduct a reaction in the dark;

[0047] S103: column chromatography purification;

[0048] S104: Prepare the target product (the structural formula is shown in formula III and formula IV)

[0049] The specific preparation method of the D-A type fluoroboron-dipyrrole conjugated polymer is as follows: the fluoroboron-dipyrrole compound is respectively reacted with an electron-donating monomer and a catalyst in an organic solvent system under the protection of an inert g...

Embodiment 1

[0072] The invention provides a method for preparing a D-A type fluoroboron dipyrrole conjugated polymer. 0.492 mmol of the compound represented by formula I and 0.738 mmol of 5,5'-bistrimethyltin-2,2'-bithiophene Place in dichloromethane solvent, use copper oxide, tris(2-tolyl)phosphine and tris(dibenzylideneacetone)dipalladium as catalysts, under the protection of inert gas, control the temperature at 110°C, and avoid light for 48h , and purified by column chromatography to obtain the target product formula III.

[0073] The synthetic route of the formula III is as follows:

[0074]

[0075] The NMR of the target product formula III is: 1 H NMR (CDCl 3 ,400MHz,δ / ppm): 7.55(br,1H), 7.14(br,3H), 7.02(br,2H), 6.78(br,1H), 2.62(br,6H), 1.58(br,6H); 13 C NMR (CDCl 3 , 100MHz, δ / ppm): 152.46, 142.85, 138.25, 135.13, 130.77, 123.56, 120.55, 118.47, 114.68, 76.15, 34.95, 33.85, 31.47, 29.54, 27.12, 16.67, 9.87.

[0076] figure 2 The ultraviolet-visible absorption spectrum ...

Embodiment 2

[0086] The invention provides a method for preparing a D-A type fluoroboron dipyrrole conjugated polymer. 0.523 mmol of the compound represented by formula II and 0.628 mmol of 5,5'-bistrimethyltin-2,2'-bithiophene Place in dichloromethane solvent, use copper oxide as catalyst, under the protection of inert gas, control the temperature at 110°C, react in the dark for 48 hours, and purify by column chromatography to obtain the target product formula IV.

[0087] The synthetic route of described formula IV is as follows:

[0088]

[0089] The NMR of the target product formula IV is: 1 H NMR (CDCl 3 ,400MHz,δ / ppm): 7.55(br,1H), 7.14(br,3H), 7.02(br,2H), 6.78(br,1H), 2.62(br,6H), 1.58(br,6H); 13 C NMR (CDCl 3 , 100MHz, δ / ppm): 152.46, 142.85, 138.25, 135.13, 130.77, 123.56, 120.55, 118.47, 114.68, 76.15, 34.95, 33.85, 31.47, 29.54, 27.12, 16.67, 9.87.

[0090] Figure 5 The ultraviolet-visible absorption spectrogram of the D-A type fluoroboron dipyrrole conjugated polymer ...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

PUM

No PUM Login to View More

Abstract

The invention provides a preparation method of a D-A type fluoroboron dipyrrole conjugated polymer. The polymer is composed of a compound with a structure shown in the formula or formula, an electron-donating monomer, and a catalyst in an organic solvent system under the protection of an inert gas , first carry out reaction in the dark, and finally use column chromatography to purify to prepare the target product. The molar ratio of the compound of the formula or the structure shown in the formula to the electron-donating monomer is 1:1-2, the reaction temperature is 90-130°C, and the time is 24-72h; the electron-donating monomer is 5,5' ‑Bistrimethyltin‑2,2'‑bithiophene, the catalyst is any one of copper oxide, tris(2-tolyl)phosphine or tris(dibenzylideneacetone)dipalladium or a mixture of any several , the organic solvent is dichloromethane. The polymer prepared by the method provided by the invention has good absorption and suitable energy level in the range of visible light, and is suitable as a donor material in an organic solar cell.

Description

technical field [0001] The invention relates to the technical field of solar cells, in particular to a preparation method and application of a D-A type fluoroboron dipyrrole conjugated polymer. Background technique [0002] So far, energy has always been an indispensable driving force for human development and progress, and the development and utilization of energy is also a long-term topic. As a clean energy source, solar energy has been favored by people for its inexhaustible and inexhaustible advantages. of favor. Among the various technologies that humans use solar energy, solar cells, that is, devices that use the "photovoltaic effect" to directly convert light energy into electrical energy, are currently widely used and one of the most promising technologies. [0003] For a long time, people have made more solar cells based on inorganic materials such as crystalline silicon, but the disadvantages of such cell production, such as complex process, high cost, high energy...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

Application Information

Patent Timeline
no application Login to View More
Patent Type & Authority Patents(China)
IPC IPC(8): C08G61/12H01L51/46
CPCC08G61/126C08G61/122C08G2261/124C08G2261/414C08G2261/91C08G2261/1424C08G2261/145C08G2261/3223C08G2261/3247C08G2261/512C08G2261/514C08G2261/18H10K85/113Y02E10/549
Inventor 赖越平何安旺秦元成邓文杰黄菲高李健刘奇秦文黄锦程冯林喜
Owner NANCHANG HANGKONG UNIVERSITY
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Patsnap Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Patsnap Eureka Blog
Learn More
PatSnap group products

Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.

© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com