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单结二元共混非富勒烯聚合物太阳能电池,效率达 12.1%。

Single-Junction Binary-Blend Nonfullerene Polymer Solar Cells with 12.1% Efficiency.

机构信息

Department of Materials Science and Engineering, College of Engineering, Key Laboratory of Polymer Chemistry and Physics of Ministry of Education, Peking University, Beijing, 100871, China.

Institute of Chemistry, Chinese Academy of Sciences, Beijing, 100190, China.

出版信息

Adv Mater. 2017 May;29(18). doi: 10.1002/adma.201700144. Epub 2017 Mar 10.

DOI:10.1002/adma.201700144
PMID:28295734
Abstract

A new fluorinated nonfullerene acceptor, ITIC-Th1, has been designed and synthesized by introducing fluorine (F) atoms onto the end-capping group 1,1-dicyanomethylene-3-indanone (IC). On the one hand, incorporation of F would improve intramolecular interaction, enhance the push-pull effect between the donor unit indacenodithieno[3,2-b]thiophene and the acceptor unit IC due to electron-withdrawing effect of F, and finally adjust energy levels and reduce bandgap, which is beneficial to light harvesting and enhancing short-circuit current density (J ). On the other hand, incorporation of F would improve intermolecular interactions through CF···S, CF···H, and CF···π noncovalent interactions and enhance electron mobility, which is beneficial to enhancing J and fill factor. Indeed, the results show that fluorinated ITIC-Th1 exhibits redshifted absorption, smaller optical bandgap, and higher electron mobility than the nonfluorinated ITIC-Th. Furthermore, nonfullerene organic solar cells (OSCs) based on fluorinated ITIC-Th1 electron acceptor and a wide-bandgap polymer donor FTAZ based on benzodithiophene and benzotriazole exhibit power conversion efficiency (PCE) as high as 12.1%, significantly higher than that of nonfluorinated ITIC-Th (8.88%). The PCE of 12.1% is the highest in fullerene and nonfullerene-based single-junction binary-blend OSCs. Moreover, the OSCs based on FTAZ:ITIC-Th1 show much better efficiency and better stability than the control devices based on FTAZ:PC BM (PCE = 5.22%).

摘要

一种新型的氟化非富勒烯受体 ITIC-Th1 已被设计和合成,其方法是在端基封端基团 1,1-二氰基甲基-3-茚满酮(IC)上引入氟(F)原子。一方面,由于 F 的吸电子效应,F 的引入会改善分子内相互作用,增强给体单元茚并二噻吩并[3,2-b]噻吩和受体单元 IC 之间的推拉效应,最终调整能级并降低带隙,这有利于光捕获并提高短路电流密度(J)。另一方面,F 的引入会通过 CF···S、CF···H 和 CF···π 非共价相互作用改善分子间相互作用,并提高电子迁移率,这有利于提高 J 和填充因子。事实上,结果表明,氟化 ITIC-Th1 表现出红移吸收、更小的光学带隙和比非氟化 ITIC-Th 更高的电子迁移率。此外,基于氟化 ITIC-Th1 电子受体和基于苯并二噻吩和苯并三唑的宽带隙聚合物给体 FTAZ 的非富勒烯有机太阳能电池(OSC)表现出高达 12.1%的功率转换效率(PCE),明显高于非氟化 ITIC-Th(8.88%)。12.1%的 PCE 在富勒烯和非富勒烯基于单结二元共混 OSC 中是最高的。此外,基于 FTAZ:ITIC-Th1 的 OSC 比基于 FTAZ:PC BM 的对照器件(PCE=5.22%)具有更好的效率和更好的稳定性。

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