接受者
离域电子
电子受体
戒指(化学)
平面度测试
化学
噻吩
分子内力
电子供体
平面的
电子
分子间力
光化学
分子
材料科学
结晶学
立体化学
有机化学
物理
计算机科学
催化作用
计算机图形学(图像)
量子力学
凝聚态物理
作者
Xinming Zheng,Wenlong Liu,Hao Lu,Na Yu,Yunzhi Wang,Hao Huang,Li Song,Xiaodong Wang,Sheng Wang,Yahui Liu,Xinjun Xu,Zheng Tang,Zhishan Bo
标识
DOI:10.1016/j.cej.2022.136472
摘要
We designed two simple fully nonfused ring electron acceptors 4T-OEH and 4T-EH with 3,4-bis(alkoxy)thiophene and 3,4-dialkylthiophene π-bridge units, respectively, which can be modularly synthesized with only four high-yield steps. With the help of intramolecular S-O noncovalent interaction, 4T-OEH tends to form a planar molecular backbone, which is beneficial for the electron delocalization and charge transport. Besides, the neat 4T-OEH film displays a more ordered molecular packing and obviously red-shifted absorption after thermal annealing. Compared with 4T-EH, 4T-OEH based devices can form more homogenous phase morphology, higher and more balanced hole and electron mobilities. The optimal OSCs based on 4T-OEH can generate an excellent PCE of 12.12%, which is much higher than 4T-OEH based ones (7.36%). It is worth noting that the figure-of-merit values of 4T-OEH is much higher than the star acceptors (ITIC and Y6), demonstrating its high potential for future practical application. Our work has demonstrated that we can tune the backbone planarity, solubility and packing behavior of acceptor molecules via optimizing their lateral substituents to obtain high efficiency and low-cost fully nonfused ring electron acceptors.
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