Controlling the Condensed Structure of Polythiophene and Polyselenophene-based All-conjugated Block Copolymers

Yue Yin; Da-long Zhai; Shu-wen Chen; Xin Shang; Li-xin Li; Juan Peng

doi:10.11777/j.issn1000-3304.2020.19220

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Controlling the Condensed Structure of Polythiophene and Polyselenophene-based All-conjugated Block Copolymers

更新时间：2021-01-26

- Controlling the Condensed Structure of Polythiophene and Polyselenophene-based All-conjugated Block Copolymers
- Acta Polymerica Sinica Vol. 51, Issue 5, Pages: 434-447(2020)
- 作者机构：
  
  聚合物分子工程国家重点实验室复旦大学高分子科学系　上海 200438
- 作者简介：
- 基金信息：
- DOI：10.11777/j.issn1000-3304.2020.19220
  CLC：
- Published：2020-5，
  
  Published Online：14 April 2020，
  
  Received：26 December 2019，
  
  Revised：11 February 2020，
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Yue Yin, Da-long Zhai, Shu-wen Chen, Xin Shang, Li-xin Li, Juan Peng. Controlling the Condensed Structure of Polythiophene and Polyselenophene-based All-conjugated Block Copolymers. [J]. Acta Polymerica Sinica 51(5):434-447(2020)
DOI：

Yue Yin, Da-long Zhai, Shu-wen Chen, Xin Shang, Li-xin Li, Juan Peng. Controlling the Condensed Structure of Polythiophene and Polyselenophene-based All-conjugated Block Copolymers. [J]. Acta Polymerica Sinica 51(5):434-447(2020) DOI： 10.11777/j.issn1000-3304.2020.19220.

摘要

嵌段共聚物可发生微相分离形成丰富的介观尺度上的相结构，而共轭聚合物是一类具有特殊的力学、导电性能或光电功能的半刚性链高分子. 全共轭嵌段共聚物因其兼具两者的特性而备受瞩目. 本文着重介绍了近年来课题组在基于全共轭聚(3-烷基噻吩)和聚(3-烷基硒吩)嵌段共聚物体系的研究进展，通过改变体系的分子结构包括主侧链结构、侧链的烷基长度及取代基团等以及对体系在溶液状态及薄膜状态进行后处理包括改变溶剂、热处理、溶剂蒸气处理等来调控体系的微相分离行为和结晶行为，实现对材料凝聚态结构的调控. 在此基础上，以有机场效应晶体管和聚合物太阳能电池器件作为最终体现聚噻吩或聚硒吩类体系凝聚态结构与性能关系的平台，将获得的调控体系凝聚态结构的有效策略用于实现其半导体材料物理性能的提升.

Abstract

Block copolymers can microphase separate into a variety of well-defined nanoscale structures. Conjugated polymers are a kind of semi-rigid macromolecules with special mechanical

conducting

and optoelectronic properties. All-conjugated block semiconducting copolymers have gained immense interest because they combine the optoelectronic properties of conjugated polymers with the fascinating self-assembly properties of block copolymers. In this feature article

we introduced some research progresses on poly(3-alkylthiophene) and poly(3-alkylselenophene)-based all-conjugated diblock copolymers

focusing on controlling the condensed structure of these two systems in our group. By tuning their molecular structures (such as main/side chains

the length of alkyl side chains and side substitutions

etc

and the post-treatment in their solution and film states (such as changing solvents

aging

thermal and solvent annealing

etc

the synergy and competition between two basic phase transitions

that is

their microphase-separated behavior and crystalline behavior were systematically studied and clarified. As a result

their condensed structures were efficiently tuned. Furthermore

their optoelectronic properties such as charge mobilities based on their different condensed structures were investigated to build up the relationship among their chemical structures

condensed structures

and device performance. As poly(3-alkylthiophene) and poly(3-alkylselenophene) are model systems with simple molecular structures

the rules and knowledge about controlling their condensed structures obtained from these model systems are expected to be applied in other conjugated systems with more complexed molecular structures and better properties.

关键词

嵌段共聚物共轭聚合物凝聚态结构微相分离光电性能

Keywords

Block copolymerConjugated polymerCondensed structureMicrophase separationOptoelectronic property

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School of Chemistry and Biological Engineering, University of Science and Technology Beijing

Beijing National Laboratory for Molecular Sciences, Key Laboratory of Polymer Chemistry and Physics of Ministry of Education, Center for Soft Matter Science and Engineering, College of Chemistry and Molecular Engineering, Peking University

Department of Materials Science and Chemical Engineering, Chizhou University

Anhui Key Laboratory of Advanced Functional Materials and Devices, School of Chemistry and Chemical Engineering, Hefei University of Technology

College of Chemical Engineering, Fuzhou University

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