材料科学
钝化
胶束
电导
共轭体系
化学物理
分子间力
纳米技术
化学工程
工作(物理)
有机太阳能电池
光电子学
聚合物
有机发光二极管
电荷(物理)
有机半导体
机制(生物学)
聚合物太阳能电池
分子动力学
电阻和电导
双层
电阻率和电导率
兴奋剂
有机电子学
分子自组装
能量转换效率
作者
Xiaxia Yang,Jingfu Tian,J Y Chen,Changsheng Mao,Dianyong Tang,Menglan Lv,Yuanpeng Xie
摘要
ABSTRACT The π‐extension strategy represents a highly effective approach toward improving the charge transport capability of self‐assembled monolayers/multilayers. Nevertheless, highly conjugated molecular backbones readily trigger intense intermolecular interactions, which further cause severe molecular aggregation and incomplete surface coverage of the assembled films. Here, we synthesized a unilateral π‐expanded self‐assembled molecule, namely (4‐(3‐(2‐chlorothiophen‐3‐yl)‐9H‐carbazol‐9‐yl)butyl)phosphonic acid) (Cl‐4PAThCz). The unilateral π‐extension design of Cl‐4PAThCz disrupts the molecular symmetry, which in turn optimizes its critical micelle concentration and micelle size in solution. This unique solution property is beneficial to the subsequent formation of a uniformly covered film without large‑scale molecular aggregation. Such a high‐quality film enables effective passivation of interfacial defects, accompanied by enhanced electrical conductance and hole transport capacity. Consequently, a champion efficiency of 20.77% (certified to 20.31%) with an outstanding fill factor of 83.16% was achieved, which is among the state‐of‐the‐art efficiencies for OSCs. This work clarifies the mechanism behind asymmetrical self‐assembled molecules, affording valuable guidance for the materials design of organic semiconductor.
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