混溶性
材料科学
烷基
有机太阳能电池
侧链
结晶度
小分子
噻唑
聚合物太阳能电池
分子
相(物质)
化学工程
光电子学
太阳能电池
有机化学
聚合物
复合材料
化学
工程类
生物化学
作者
Kun Ma,Wanying Feng,Huazhe Liang,Hongbin Chen,Yuxin Wang,Xiangjian Wan,Zhaoyang Yao,Chenxi Li,Bin Kan,Yongsheng Chen
标识
DOI:10.1002/adfm.202214926
摘要
Abstract Molecular innovation is highly desirable to achieve efficient all‐small‐molecule organic solar cells (SM‐OSCs). Herein, three small‐molecule donors (SMDs) with alkylated thiazole side groups (namely BO‐1, HD‐1, and OD‐1), which differ only in the alkyl side chain are reported. Although these SMDs possess similar absorption profiles and molecular energy levels, their crystallinity and miscibility with BTP‐eC9 slightly decrease along with the elongation of the alkyl side chain. After blending with BTP‐eC9, different miscibility leads to different degrees of phase separation. Among these SM‐OSCs, the HD‐1‐based device shows a decent bulk‐heterojunction (BHJ) morphology with proper phase separation and more dynamic carrier behavior. Thus, compared to the BO‐1 and OD‐1‐based devices, the HD‐1‐based device achieves a higher short‐circuit current of 26.04 mA cm −2 and a fill factor of 78.46%, leading to an outstanding PCE of 17.19%, which is one of the highest values among SM‐OSCs. This work provides a rational design strategy of SMDs for highly efficient SM‐OSCs.
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