Effect of electron-withdrawing side chain modifications on the optical properties of thiophene-quinoxaline acceptor based polymers

被引:28
作者
Kroon, Renee [1 ]
Lundin, Angelica [1 ]
Lindqvist, Camilla [1 ]
Henriksson, Patrik [1 ]
Steckler, Timothy T. [1 ]
Andersson, Mats R. [1 ]
机构
[1] Chalmers, Dept Chem & Biol Engn, S-41296 Gothenburg, Sweden
基金
瑞典研究理事会;
关键词
Conjugated polymers; Side chain modification; Energy level engineering; PI-CONJUGATED POLYMERS; SOLAR-CELLS; PERFORMANCE;
D O I
10.1016/j.polymer.2013.01.003
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Four new thiophene-quinoxaline acceptor based polymers have been synthesized. The parent thiophene-quinoxaline acceptor based copolymer was modified by introducing different electron-withdrawing groups adjacent to the thiophene side group. The effect on the physical, electrochemical and optical properties of the polymer series is discussed with respect to the parent thiophene-quinoxaline acceptor based polymer. The side chain carbonyl from one modified monomer could conveniently be transformed to either a difluoromethylene or an -ylidene malononitrile group via carbonyl transformations. For all polymers incorporating an electron-withdrawing side group both the HOMO and especially the LUMO were significantly shifted away from vacuum while all exhibit enhanced light harvesting ability. Especially the incorporation of an -ylidine malononitrile side group increases both the spectral coverage and absorption coefficient. Incorporation of a difluoromethylene side group resulted in a twofold increase of the molecular weight compared to the parent polymer structure. (c) 2013 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1285 / 1288
页数:4
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