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Synthesis of a tetrazine–quaterthiophene copolymer and its optical structural and photovoltaic properties

机译:四嗪-四噻吩共聚物的合成及其光学结构和光伏性质

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摘要

Herein, we report the synthesis of a novel, tetrazine-based conjugated polymer. Tetrazines have the benefit of being strong electron acceptors, while little steric hindrance is imposed on the flanking thiophene rings. Conversion of a suitably substituted nitrile precursor led to 3,6-bis(5-bromo-4-(2-octyldodecyl)thiophen-2-yl)-1,2,4,5-tetrazine (2OD-TTz). Palladium-catalyzed copolymerization of 2OD-TTz with a bithiophene monomer yielded an alternating tetrazine–quaterthiophene copolymer (PTz4T-2OD). The polymer PTz4T-2OD showed an optical band gap of 1.8 eV, a deep HOMO energy level of − 5.58 eV and good solubility. In combination with the non-fullerene acceptor ITIC-F, solar cells with power conversion efficiencies of up to 2.6% were obtained.Electronic supplementary materialThe online version of this article (10.1007/s10853-019-03551-3) contains supplementary material, which is available to authorized users.
机译:在此,我们报道了一种新颖的基于四嗪的共轭聚合物的合成。四嗪具有成为强电子受体的优势,而侧翼噻吩环几乎没有空间位阻。适当取代的腈前体的转化导致3,6-双(5-溴-4-(2-辛基十二烷基)噻吩-2-基)-1,2,4,5-四嗪(2OD-TTz)。钯催化的2OD-TTz与联苯噻吩单体的共聚反应产生了交替的四嗪-四联噻吩共聚物(PTz4T-2OD)。聚合物PTz4T-2OD的光学带隙为1.8 eV,深HOMO能级为-5.58 eV,溶解度良好。结合非富勒烯受体ITIC-F,可获得功率转换效率高达2.6%的太阳能电池。电子补充材料本文的在线版本(10.1007 / s10853-019-03551-3)包含补充材料,其中适用于授权用户。

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