结晶度
有机太阳能电池
接受者
位阻效应
分子间力
溴
氯
氟
分子
材料科学
化学
光化学
结晶学
有机化学
聚合物
物理
凝聚态物理
作者
Huazhe Liang,Xingqi Bi,Hongbin Chen,Tengfei He,Yi Lin,Yunxin Zhang,Kangqiao Ma,Wanying Feng,Zaifei Ma,Guankui Long,Chenxi Li,Bin Kan,Hongtao Zhang,Олег А. Ракитин,Xiangjian Wan,Zhaoyang Yao,Yongsheng Chen
标识
DOI:10.1038/s41467-023-40423-6
摘要
Abstract Given that bromine possesses similar properties but extra merits of easily synthesizing and polarizing comparing to homomorphic fluorine and chlorine, it is quite surprising very rare high-performance brominated small molecule acceptors have been reported. This may be caused by undesirable film morphologies stemming from relatively larger steric hindrance and excessive crystallinity of bromides. To maximize the advantages of bromides while circumventing weaknesses, three acceptors (CH20, CH21 and CH22) are constructed with stepwise brominating on central units rather than conventional end groups, thus enhancing intermolecular packing, crystallinity and dielectric constant of them without damaging the favorable intermolecular packing through end groups. Consequently, PM6:CH22-based binary organic solar cells render the highest efficiency of 19.06% for brominated acceptors, more excitingly, a record-breaking efficiency of 15.70% when further thickening active layers to ~500 nm. By exhibiting such a rare high-performance brominated acceptor, our work highlights the great potential for achieving record-breaking organic solar cells through delicately brominating.
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