接受者
材料科学
有机太阳能电池
方向(向量空间)
分子
聚合物
电子受体
化学
光化学
有机化学
物理
数学
复合材料
几何学
凝聚态物理
作者
Yunlong Ma,Ming Zhang,Shuo Wan,Pan Yin,Pengsong Wang,Dongdong Cai,Feng Liu,Qingdong Zheng
出处
期刊:Joule
[Elsevier]
日期:2020-12-04
卷期号:5 (1): 197-209
被引量:199
标识
DOI:10.1016/j.joule.2020.11.006
摘要
Summary
A "face-on" molecular orientation is essential for photovoltaic materials with efficient vertical carrier transport, but understanding how the molecular structures control their orientations remains challenging. Based on a ladder-type fused-ring core without sp3-hybridized bridging atoms, novel acceptor-donor-acceptor (A-D-A or ADA)-type nonfullerene acceptors (M3 and M32) are developed, and their molecular orientation behaviors are successfully controlled by the neighboring side chains. With linear n-cetyl chains on the nitrogen atoms, the acceptor (M32) tends to adopt an "edge-on" molecular orientation, whereas with bulky branched 2-hexyldecyl chains, the acceptor (M3) has a preferred "face-on" orientation. Blended with a donor polymer of PM6, M3 shows optimal phase separation and dramatically improved electron transport, consequently leading to a much higher device performance than M32. Further optimization of the M3-based devices yields an outstanding efficiency of 16.66%. The strategy of molecular orientation control proposed here will inspire many other innovative designs and syntheses of high-performance nonfullerene acceptors.
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