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具有噻吩侧链的高性能电子受体用于有机光伏

High-Performance Electron Acceptor with Thienyl Side Chains for Organic Photovoltaics.

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.

Department of Chemistry, Capital Normal University , Beijing 100048, China.

出版信息

J Am Chem Soc. 2016 Apr 13;138(14):4955-61. doi: 10.1021/jacs.6b02004. Epub 2016 Apr 1.

Abstract

We develop an efficient fused-ring electron acceptor (ITIC-Th) based on indacenodithieno[3,2-b]thiophene core and thienyl side-chains for organic solar cells (OSCs). Relative to its counterpart with phenyl side-chains (ITIC), ITIC-Th shows lower energy levels (ITIC-Th: HOMO = -5.66 eV, LUMO = -3.93 eV; ITIC: HOMO = -5.48 eV, LUMO = -3.83 eV) due to the σ-inductive effect of thienyl side-chains, which can match with high-performance narrow-band-gap polymer donors and wide-band-gap polymer donors. ITIC-Th has higher electron mobility (6.1 × 10(-4) cm(2) V(-1) s(-1)) than ITIC (2.6 × 10(-4) cm(2) V(-1) s(-1)) due to enhanced intermolecular interaction induced by sulfur-sulfur interaction. We fabricate OSCs by blending ITIC-Th acceptor with two different low-band-gap and wide-band-gap polymer donors. In one case, a power conversion efficiency of 9.6% was observed, which rivals some of the highest efficiencies for single junction OSCs based on fullerene acceptors.

摘要

我们开发了一种基于茚并二噻吩[3,2-b]噻吩核心和噻吩侧链的高效稠环电子受体(ITIC-Th),用于有机太阳能电池(OSCs)。与具有苯基侧链的 ITIC 相比(ITIC),由于噻吩侧链的σ-诱导效应,ITIC-Th 的能级较低(ITIC-Th:HOMO = -5.66 eV,LUMO = -3.93 eV;ITIC:HOMO = -5.48 eV,LUMO = -3.83 eV),可以与高性能的窄带隙聚合物给体和宽带隙聚合物给体匹配。由于硫-硫相互作用引起的分子间相互作用增强,ITIC-Th 的电子迁移率(6.1×10(-4)cm(2)V(-1)s(-1))高于 ITIC(2.6×10(-4)cm(2)V(-1)s(-1))。我们通过将 ITIC-Th 受体与两种不同的低带隙和宽带隙聚合物给体共混来制备 OSCs。在一种情况下,观察到 9.6%的功率转换效率,这与基于富勒烯受体的单结 OSCs 的一些最高效率相当。

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