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首页> 外文期刊>Journal of Polymer Science, Part A. Polymer Chemistry >4,9-dihydro-s-indaceno[1,2-b : 5,6-b']dithiophene-4,9-dione functionalized copolymers for organic photovoltaic devices
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4,9-dihydro-s-indaceno[1,2-b : 5,6-b']dithiophene-4,9-dione functionalized copolymers for organic photovoltaic devices

机译:用于有机光伏器件的4,9-二氢-s-茚满[1,2-b:5,6-b']二噻吩-4,9-二酮官能化共聚物

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The synthesis of conjugated polymers 1-5 functionalized with 4,9-dihydro-s-indaceno[1,2-b:5,6-b']dithiophene-4,9-dione in the backbone is reported and their use in the construction of organic solar cells is demonstrated. Increasing the molar ratio of 2,7-dibromo-3,8-dihexyl-4,9-dihydro-s-indaceno[1,2-b:5,6-b']dithiophene4,9-dione, relative to 4,4'-dihexyl-5,5'-dibromo-2,2'-bithiophene, in the copolymer synthesis significantly lowers the solubility of these polymers. The incorporation of highly conjugated 3,8-dihexyl-4,9-dihydro-s-indaceno[1,2-b:5,6-b']dithiophene-4,9-dione unit into the polymer backbone has been confirmed by UV-vis absorption. The observation of decreasing quantum yield for the emission in the order of 1, 2, 3 is consistent with copolymers with different comonomer content. The power conversion efficiencies of solar cells using blends of these polymers with PCBM ([6,6]-phenyl C-61-butyric acid methyl ester) were determined to be 0.11% for polymer 1, 0.33% for 2, and 0.26% for 3, respectively. Under identical white light illumination, the power conversion efficiency of the device based on polymer 2/PCBM as the active layer was three times higher compared to that of device based on polymer 1/PCBM. Owing to the limited solubility and poor film-forming ability of polymer 3, the power conversion efficiency of solar cell based on 3/PCBM blend is lower than that of 2/PCBM blend, but is still larger than that of 1/PCBM blend. (c) 2008 Wiley Periodicals, Inc.
机译:报道了在骨架中用4,9-二氢-s-茚满[1,2-b:5,6-b']二噻吩-4,9-二酮官能化的共轭聚合物1-5的合成及其在合成中的用途证明了有机太阳能电池的构造。相对于4 ,,增加2,7-二溴-3,8-二己基-4,9-二氢-s-茚满[1,2-b:5,6-b']二噻吩4,9-二酮的摩尔比共聚物合成中的4'-二己基-5,5'-二溴-2,2'-联噻吩显着降低了这些聚合物的溶解度。高度共轭的3,8-二己基-4,9-二氢-s-茚二酮[1,2-b:5,6-b']二噻吩-4,9-二酮单元掺入聚合物骨架已得到证实紫外线吸收。观察到以1、2、3的量级降低发射的量子产率与具有不同共聚单体含量的共聚物一致。使用这些聚合物与PCBM([6,6]-苯基C-61-丁酸甲酯)的共混物测得的太阳能电池的功率转换效率为:聚合物1为0.11%,聚合物2为0.33%,聚合物1为0.26%。 3,分别。在相同的白光照射下,基于聚合物2 / PCBM作为有源层的器件的功率转换效率是基于聚合物1 / PCBM的器件的三倍。由于聚合物3的有限的溶解度和较差的成膜能力,基于3 / PCBM共混物的太阳能电池的功率转换效率低于2 / PCBM共混物的功率转换效率,但仍大于1 / PCBM共混物的功率转换效率。 (c)2008年Wiley Periodicals,Inc.

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