有机太阳能电池
材料科学
相(物质)
电子受体
结晶度
三元运算
接受者
化学工程
有机电子学
聚合物
共轭体系
光化学
有机化学
化学
物理
复合材料
晶体管
量子力学
电压
计算机科学
工程类
程序设计语言
凝聚态物理
作者
Bo Wang,Jianing Xu,Yi Lin,Chengyi Xiao,Shijie Liang,Zheng Tang,Christopher R. McNeill,Weiwei Li
标识
DOI:10.1002/adfm.202418659
摘要
Abstract Star‐shaped conjugated materials exhibit monodisperses, well‐defined structures akin to small molecules while possessing the high molecular weights typical of polymers, making them appealing for organic electronics. Herein, a series of star‐shaped electron acceptors, labeled SP1‐Ph, SP2‐Ph, SP3‐Ph, SP4‐Ph, and SP6‐Ph correspond to one to six number of arms, have been synthesized for use in organic solar cells (OSCs). The acceptors have been synthesized through Williamson ether synthesis, utilizing OH‐substituted Y‐type precursors and (multiple‐substituted bromomethyl)benzene. An increase in the number of arms results in weakened crystallinity and different aggregation behavior. Therefore, different number of arms can efficiently tune phase separation sizes between the acceptors and donor polymer blended films, which dominates the charge generation process in OSCs. As a result, SP3‐Ph and SP4‐Ph, with modest phase separation size in binary blends, have achieved optimal efficiencies of 16.10% with high stability. However, SP6‐Ph‐based OSC exhibits oversized phase separation and low efficiency of 8.87%. Furthermore, the use of SP3‐Ph and SP4‐Ph in ternary OSCs leads to an impressive efficiency of 19.3%. These results highlight the ability of star‐shaped electron acceptors with varying arm numbers to precisely control the phase separation of photoactive layers, thereby advancing the development of highly efficient and stable OSCs.
科研通智能强力驱动
Strongly Powered by AbleSci AI