堆积
三噻吩
有机太阳能电池
材料科学
噻吩
接受者
光化学
电子受体
共轭体系
聚合物太阳能电池
位阻效应
分子间力
能量转换效率
离域电子
深铬移
二氯苯
轨道能级差
有机半导体
电子供体
拉曼光谱
聚合物
有机电子学
吸收(声学)
三联烯
光电流
吸收光谱法
结晶学
作者
Kexin Zhao,Wen Ma,Shuaishuai Shen,Ningfang Zhang,Rongyue Zhang,W W Liu,Wenjun Zhang,Jinsheng Song
标识
DOI:10.1021/acs.chemmater.6c00715
摘要
Nonfused ring electron acceptors (NFREAs) have emerged as promising candidates for high-efficiency organic solar cells, owing to their cost-effectiveness. Notably, the number of aromatic rings in their nonfused conjugated backbones plays a crucial role in determining optical and electronic properties, as well as molecular packing and orientation. Herein, a simple terthiophene backbone was employed to construct the asymmetric acceptor R3T-4F via a macrocyclic encapsulation strategy, while I3T-4F with the traditional sterically hindered substituents was designed as a control molecule. With the symmetry breaking, both acceptors exhibited multiple π–π stacking modes with hierarchical characteristics, whereas an even more compact packing was achieved by R3T-4F, significantly facilitating intermolecular charge transport and resulting in a pronounced bathochromic shift in the absorption spectrum. Furthermore, the R3T-4F blend film exhibits a well-defined nanofiber network morphology, effectively suppressing charge recombination and enhancing the charge transport. As a result, devices based on R3T-4F achieved the highest power conversion efficiency (PCE) of 15.04% among the terthiophene-based acceptors and exhibited excellent “unit economy” for the individual contribution of each thiophene unit to photovoltaic performances.
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