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

Polymer, preparation method thereof and organic polymer solar battery

A polymer and compound technology, applied in circuits, photovoltaic power generation, electrical components, etc., can solve problems such as low utilization rate, low battery efficiency, and narrow absorption band of conjugated compounds

Active Publication Date: 2013-12-11
CHANGCHUN INST OF APPLIED CHEMISTRY - CHINESE ACAD OF SCI
View PDF4 Cites 4 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0005] The low utilization rate of the solar spectrum and the low charge carrier mobility of conjugated polymers are the main reasons for the low efficiency of current batteries. Due to the narrow absorption bands of existing conjugated compounds, the solar spectrum cannot be effectively used, and at the same time Causes the hole mobility of the conjugated polymer to be relatively low

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
  • Polymer, preparation method thereof and organic polymer solar battery
  • Polymer, preparation method thereof and organic polymer solar battery
  • Polymer, preparation method thereof and organic polymer solar battery

Examples

Experimental program
Comparison scheme
Effect test

preparation example Construction

[0036] The present invention also provides a preparation method of a polymer represented by formula (I), comprising the following steps: under the condition of inert gas protection, combining a compound having a structure of formula (III-1) with a compound having a structure of formula (IV) The compound is mixed under the action of a catalyst and an auxiliary ligand, and reacted to obtain a polymer represented by formula (I);

[0037]

[0038] Among them, R 1 is an alkyl group; R 2 Is an alkyl group; X is H or a fluorine atom; n is the degree of polymerization.

[0039] In the present invention, the R 1 , R 2 , X and n are the same as above, and will not be repeated here.

[0040] The present invention has no special limitation on the sources of all raw materials, which can be commercially available or self-made.

[0041] The compound with the structure of formula (IV) is preferably prepared according to the following method: S1) The compound with the structure of form...

Embodiment 1

[0062] 1.1 Under argon atmosphere, add 16.39mmol 6-bromoindol-2-one and 16.39mmol 6-bromo-7-fluoroisatin to a 250ml three-necked flask, add 200ml glacial acetic acid and 1.2ml concentrated hydrochloric acid, and heat to 130 React at ℃ for 24 hours, cool to room temperature, filter, wash with water, ethanol, and ether in turn, and the red solid that is drained is 6,6′-dibromo-7-fluoroisoindigo, with a yield of 70%.

[0063] 1.2 Dissolve 2.28mmol of 6,6′-dibromo-7-fluoroisoindigo obtained in 1.1 and 9.13mmol of potassium hydroxide in 40ml of DMF, and add 9.13mmol of 1-iodo-2- Octyldodecane and 40ml THF were slowly dropped into the reaction solution, and after 24 hours of reaction at room temperature, poured into water, extracted with chloroform, and dried the organic layer with anhydrous magnesium sulfate. After washing with petroleum ether and dichloromethane as the eluent, the red solid is N,N'-bis(2-octyldodecyl)-6,6'-dibromo-7-fluoroisoindigo, Yield 42%.

[0064] 1.3 Under...

Embodiment 2

[0073] 2.1 Under argon atmosphere, add 16.39mmol 6-bromoindol-2-one and 16.39mmol 6-bromo-7-fluoroisatin into a 250ml three-necked flask, add 200ml glacial acetic acid and 1.2ml concentrated hydrochloric acid, heat to 130 React at ℃ for 24 hours, cool to room temperature, filter, wash with water, ethanol, and ether in turn, and the red solid that is drained is 6,6′-dibromo-7-fluoroisoindigo, with a yield of 70%.

[0074] 2.2 Dissolve 2.28mmol of 6,6′-dibromo-7-fluoroisoindigo obtained in 2.1 and 9.13mmol of potassium hydroxide in 40ml of DMF, and add 9.13mmol of 1-iodo-2- Butyl octane and 40ml THF were slowly dripped into the reaction liquid, and after reacting at room temperature for 24 hours, they were poured into water, extracted with chloroform, and the organic layer was dried over anhydrous magnesium sulfate. After rinsing with ether and dichloromethane as the eluent, a red solid was obtained which was N,N'-bis(2-butyloctyl)-6,6'-dibromo-7-fluoroisoindigo, and the yield w...

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

PropertyMeasurementUnit
Thicknessaaaaaaaaaa
Thicknessaaaaaaaaaa
Thicknessaaaaaaaaaa
Login to View More

Abstract

The invention provides a polymer, a preparation method thereof and an organic polymer solar battery. The polymer is shown in a formula (I) or a formula (II). Compared with an existing conjugated polymer, the polymer which is shown in the formula (I) or the formula (II) has the advantages that a condensed ring unit of dithieno carbazole serves as a donor and is low in reorganization energy and good in pi electron delocalization; by introducing the condensed ring unit into a conjugated compound, the reorganization energy of the polymer can be effectively reduced, and the conjugation length of the polymer is increased, so that the mobility of the polymer can be improved, and an optical band gap of the polymer is reduced; the optical band gap is reduced to cause the red shift of an absorption band of the polymer, and absorption spectra are matched with solar spectra. Therefore, by the adoption of the polymer, the spectrum absorption range of the polymer can be expanded, and the hole mobility can be improved; fluoro-isoindigo serves as a receptor, so that the highest occupied molecular orbital (HOMO) energy level of the polymer can be reduced, and the open-circuit voltage of the polymer solar battery is improved.

Description

technical field [0001] The invention belongs to the technical field of semiconductor materials, and in particular relates to a polymer, a preparation method thereof, and an organic polymer solar cell. Background technique [0002] Compared with traditional silicon solar cells, organic polymer solar cells have attracted much attention due to their advantages of light weight, low cost, large-area processing and flexible devices. [0003] Organic polymer solar cells are usually composed of positive and negative electrodes and a thin photoactive layer between them. The photoactive thin layer is generally a bulk heterojunction (BHJ) structure composed of a donor (D) and an acceptor (A). . The currently used acceptor materials mainly include CdSe, n-type polymer, C60 and its derivative PCBM, among which PCBM is the most used. The positive and negative electrodes of the BHJ type solar cell are indium tin oxide (ITO) and a metal with a lower functional function, respectively, and ...

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
IPC IPC(8): C08G61/12H01L51/46
CPCY02E10/549
Inventor 耿延候谢志元邓云峰田洪坤
Owner CHANGCHUN INST OF APPLIED CHEMISTRY - CHINESE ACAD OF SCI
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