苝
二亚胺
材料科学
有机太阳能电池
三苯基膦
聚合物太阳能电池
结晶度
超分子化学
聚合物
分子
高分子化学
光化学
化学
有机化学
催化作用
复合材料
作者
Guangjun Zhang,Jirui Feng,Xiaopeng Xu,Wei Ma,Ying Li,Qiang Peng
标识
DOI:10.1002/adfm.201906587
摘要
Abstract A series of perylene diimide (PDI) derivatives, TPP‐PDI , TPO‐PDI , and TPS‐PDI , are developed for nonfullerene polymer solar cells (NF‐PSCs) by flaking three PDI skeletons around 3D central cores with different configurations and electronic states, such as triphenylphosphine (TPP), triphenylphosphine monoxide (TPO), and triphenylphosphine sulfide (TPS). These small‐molecule acceptors have a “three‐wing propeller” structure due to their similar backbones. By changing the electron density of phosphorus atoms through oxidation and sulfuration, the “folding‐back” strength is decreased, resulting in a less twisted molecular conformation. The stronger electron‐withdrawing ability of the oxygen atom affords TPO‐PDI the least twisted conformation, which enhances the crystallinity of this complex. NF‐PSCs based on PTTEA : TPO‐PDI exhibit a high power conversion efficiency (PCE) of 8.65%. Ultimately, the joint “molecular lock” effect arising from OH⋅⋅⋅F and OH⋅⋅⋅OP supramolecular interactions is achieved by introducing 4,4′‐biphenol as an additive, which successfully promotes fibril‐like phase separation and blend morphology optimization to generate the highest PCE of 11.01%, which is currently the highest value recorded for NF‐PSCs based on PDI acceptors.
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