分子内力
非共价相互作用
戒指(化学)
有机太阳能电池
化学
纳米技术
电子
材料科学
组合化学
分子
立体化学
聚合物
有机化学
氢键
物理
量子力学
作者
Xin Zhang,Linqing Qin,Jianwei Yu,Yuhao Li,Yanan Wei,Xingzheng Liu,Xinhui Lu,Feng Gao,Hui Huang
标识
DOI:10.1002/anie.202100390
摘要
Abstract Noncovalently fused‐ring electron acceptors (NFREAs) have attracted much attention in recent years owing to their advantages of simple synthetic routes, high yields and low costs. However, the efficiencies of NFREAs based organic solar cells (OSCs) are still far behind those of fused‐ring electron acceptors (FREAs). Herein, a series of NFREAs with S⋅⋅⋅O noncovalent intramolecular interactions were designed and synthesized with a two‐step synthetic route. Upon introducing π‐extended end‐groups into the backbones, the electronic properties, charge transport, film morphology, and energy loss were precisely tuned by fine‐tuning the degree of multi‐fluorination. As a result, a record PCE of 14.53 % in labs and a certified PCE of 13.8 % for NFREAs based devices were obtained. This contribution demonstrated that combining the strategies of noncovalent conformational locks and π‐extended end‐group engineering is a simple and effective way to explore high‐performance NFREAs.
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