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Crowning of dibenzosilole with a naphthalenediimide functional group to prepare an electron acceptor for organic solar cells

机译:用萘二甲酰亚胺官能团加冠二苯并甲硅烷基以制备有机太阳能电池的电子受体

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摘要

A novel, solution-processable non-fullerene electron acceptor 9,9′-(5,5-dioctyl-5H-dibenzo [b,d]silole-3,7-diyl)bis(2,7-dioctyl-4-(octylamino)benzo[lmn][3,8]phenanthroline-1,3,6,8(2H,7H)-tetraone) (B3) based on dibenzosilole and naphthalenediimide building blocks was designed, synthesized, characterized and successfully used in a bulk-heterojunction organic solar cell. B3 displayed excellent solubility, thermal stability and acquired electron energy levels matching with those of archetypal donor polymer poly(3-hexylthiophene). Solution-processable bulk-heterojunction devices afforded 1.16% power conversion efficiency with a high fill factor of 53%. B3 is the first example in the literature using this design principle, where mild donor units at the peripheries of end-capped naphthalenediimide units tune solubility and optical energy levels simultaneously.
机译:新型的可溶液处理的非富勒烯电子受体9,9'-(5,5-二辛基-5H-二苯并[b,d]硅烷基-3,7-二基)双(2,7-二辛基-4-(设计,合成,表征并成功地将基于二苯甲酚和萘二酰亚胺的辛基氨基)苯并[lmn] [3,8]菲咯啉-1,3,6,8(2H,7H)-四酮)(B3)用于批量-异质结有机太阳能电池。 B3表现出优异的溶解性,热稳定性和获得的电子能级,与原型供体聚合物聚(3-己基噻吩)相当。可溶液处理的体异质结器件可提供1.16%的功率转换效率,且填充系数高达53%。 B3是使用该设计原理的文献中的第一个例子,其中在封端的萘二酰亚胺单元周围的温和施主单元同时调节溶解度和光能水平。

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