Novel copolymers based on PEO bridged thiophenes and 3,4-ethylenedioxythiophene: Electrochemical, optical, and electrochromic properties

被引:27
作者
Liu, Xiaofang [1 ]
Hu, Yongjing [1 ]
Shen, Lanlan [1 ]
Zhang, Ge [1 ]
Cao, Tianmin [1 ]
Xu, Jingkun [1 ,2 ]
Zhao, Feng [1 ]
Hou, Jian [3 ]
Liu, Huixuan [1 ]
Jiang, Fengxing [1 ]
机构
[1] Jiangxi Sci & Technol Normal Univ, Jiangxi Key Lab Organ Chem, Nanchang 330013, Jiangxi, Peoples R China
[2] Qingdao Univ Sci & Technol, Coll Chem & Mol Engn, Qingdao 266042, Peoples R China
[3] Luoyang Ship Mat Res Inst, State Key Lab Marine Corros & Protect, Qingdao 266101, Peoples R China
基金
中国国家自然科学基金;
关键词
PEO; Ionic conductivity; Copolymerization; Electrochromic properties; MULTICHROMIC COPOLYMER; POLYETHYLENE OXIDE; CONDUCTING POLYMER; FILMS; ELECTROSYNTHESIS; POLYTHIOPHENE; POLYANILINE; PERFORMANCE; DEVICES; ROD;
D O I
10.1016/j.electacta.2018.08.072
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Polythiophene, one of excellent conducting polymers, has attracted great concern as organic electrochromic materials. The electrochromic properties not only depend on the electron transfer of polymers, but also on the ability of ionic conduction in electrolyte. Hence, we designed a new structure of two thiophenyl monomers linked by polyethylene oxide (PEO) and prepared a new copolymer with 3,4-ethylenedioxythiophene (EDOT), which contributes to the easy deposition of the free-standing films by means of electrochemical copolymerization. PEO is of great importance for improving the electrochemical activity. On the one hand, PEO promotes the formation of crosslinking structure leading to a high-quality film. On the other hand, PEO as a soft segment ameliorates the ion-conducting capacity of polymer resulting in the better coloration efficiency (CE) and shorter response time. The as-synthesized films show excellent electrochemical active and electrochromic properties. This work proposes a new strategy of designing and preparing high-quality organic electrochromic material in the future. (C) 2018 Elsevier Ltd. All rights reserved.
引用
收藏
页码:52 / 60
页数:9
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