Isomerically Pure Benzothiophene-Incorporated Acceptor: Achieving Improved Voc and Jsc of Nonfullerene Organic Solar Cells via End Group Manipulation

苯并噻吩 丙二腈 噻吩 接受者 电子受体 堆积 有机太阳能电池 轨道能级差 Knoevenagel冷凝 硝基 化学 材料科学 立体化学 光化学 有机化学 分子 物理 聚合物 凝聚态物理 催化作用 烷基
作者
Shao-Ling Chang,Kai-En Hung,Fong‐Yi Cao,Kuo‐Hsiu Huang,Chain‐Shu Hsu,Chuang-Yi Liao,Chia‐Hao Lee,Yen‐Ju Cheng
出处
期刊:ACS Applied Materials & Interfaces [American Chemical Society]
卷期号:11 (36): 33179-33187 被引量:49
标识
DOI:10.1021/acsami.9b08462
摘要

Benzene-based 1,1-dicyanomethylene-3-indanone (IC) derivatives have been widely utilized as the end-group to construct acceptor–donor–acceptor type nonfullerene acceptors (A–D–A type NFAs). The extension of the end-group conjugation of nonfullerene acceptors (NFAs) is a rational strategy to facilitate intermolecular stacking of the end-groups which are responsible for efficient electron transportation. A bicyclic benzothiophene-based end-group acceptor, 2-(3-oxo-2,3-dihydro-1H-benzo[b]cyclopenta[d]thiophen-1-ylidene)malononitrile, denoted as α-BC was designed and synthesized. The Knoevenagel condensation of the unsymmetrical 1,3-diketo-precursor with one equivalent of malononitrile selectively reacts with the keto group attached at the α-position of the thiophene unit, leading to the isomerically pure benzothiophene-fused α-BC. The well-defined α-BC with extended conjugation was condensed with three different ladder-type diformylated donors to form three new A–D–A NFAs named BDCPDT-BC, DTCC-BC, and ITBC, respectively. The corresponding IC-based BDCPDT-IC, DTCC-IC, and ITIC model compounds were also synthesized for comparison. The incorporation of the electron-rich benzothiophene unit in the end-group upshifts the lowest unoccupied molecular orbital energy levels of the NFAs, which beneficially enlarges the Voc values. On the other hand, the benzothiophene unit in α-BC not also imparts an optical transition in the shorter wavelengths around 340–400 nm for a better light harvesting ability but also promotes the antiparallel π–π stacking of the end-groups for efficient electron transport. The organic photovoltaic cell devices using a PBDB-T polymer and BC-based NFAs all showed the improved Voc and Jsc values. The BDCPDT-BC- and DTCC-BC-based devices exhibited a power conversion efficiency (PCE) of 10.82 and 10.74%, respectively, which outperformed the corresponding BDCPDT-IC-, and DTCC-IC-based devices (9.33 and 9.25%). More importantly, the ITBC-based device delivered the highest PCE of 12.07% with a Jsc of 19.90 mA/cm2, a Voc of 0.94 V, and an fill factor of 64.51%, representing a 14% improvement relative to the traditional ITIC-based device (10.05%).

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