化学
结晶度
能量转换效率
激子
共轭体系
戒指(化学)
离解(化学)
光化学
接受者
芳基
光电子学
聚合物
有机化学
结晶学
烷基
物理
量子力学
凝聚态物理
作者
Bo Liu,Congqi Li,Xiaobin Gu,Yinghui Han,Zhixiang Wei,Yunhao Cai,Xin Zhang,Hui Huang,Yanping Huo
标识
DOI:10.1002/cjoc.202300542
摘要
Comprehensive Summary By employing the asymmetric end‐group engineering, an asymmetric nonfused‐ring electron acceptor (NFREA) was designed and synthesized. Compared with the symmetric analogs (NoCA‐17 and NoCA‐18), NoCA‐19 possesses broader light absorption range, more coplanar π‐conjugated backbone, and appropriate crystallinity according to the experimental and theoretical results. The organic solar cells based on J52:NoCA‐19 exhibited a power conversion efficiency as high as 12.26%, which is much higher than those of J52:NoCA‐17 (9.50%) and J52:NoCA‐18 (11.77%), mainly due to more efficient exciton dissociation, better and balanced charge mobility, suppressed recombination loss, shorter charge extraction time, longer charge carrier lifetimes, and more favorable blend film morphology. These findings demonstrate the great potential of asymmetric end‐group engineering in exploring low‐cost and high‐performance NFREAs.
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