堆积
超分子化学
平面度测试
有机太阳能电池
电子受体
富勒烯
戒指(化学)
接受者
分子
材料科学
小分子
化学
能量转换效率
纳米技术
聚合物
光化学
结晶学
有机化学
光电子学
物理
生物化学
凝聚态物理
作者
Yahui Liu,Cai’e Zhang,Dan Hao,Zhe Zhang,Liangliang Wu,Miao Li,Shiyu Feng,Xinjun Xu,Feng Liu,Xuebo Chen,Zhishan Bo
标识
DOI:10.1021/acs.chemmater.8b01319
摘要
Three novel non-fullerene small molecular acceptors ITOIC, ITOIC-F, and ITOIC-2F were designed and synthesized with easy chemistry. The concept of supramolecular chemistry was successfully used in the molecular design, which includes noncovalently conformational locking (via intrasupramolecular interaction) to enhance the planarity of backbone and electrostatic interaction (intersupramolecular interaction) to enhance the π–π stacking of terminal groups. Fluorination can further strengthen the intersupramolecular electrostatic interaction of terminal groups. As expected, the designed acceptors exhibited excellent device performance when blended with polymer donor PBDB-T. In comparison with the parent acceptor molecule DC-IDT2T reported in the literature with a power conversion efficiency (PCE) of 3.93%, ITOIC with a planar structure exhibited a PCE of 8.87% and ITOIC-2F with a planar structure and enhanced electrostatic interaction showed a quite impressive PCE of 12.17%. Our result demonstrates the importance of comprehensive design in the development of high-performance non-fullerene small molecular acceptors.
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