单层
材料科学
胶束
自组装单层膜
钙钛矿(结构)
两亲性
基质(水族馆)
分子
氧化铟锡
自组装
化学工程
纳米技术
临界胶束浓度
水溶液
有机化学
图层(电子)
化学
海洋学
地质学
工程类
共聚物
复合材料
聚合物
作者
Ming Liu,Le‐Yu Bi,Wenlin Jiang,Zixin Zeng,Sai‐Wing Tsang,Francis Lin,Alex K.‐Y. Jen
标识
DOI:10.1002/adma.202304415
摘要
Self-assembled monolayers (SAMs) are widely employed as effective hole-selective layers (HSLs) in inverted perovskite solar cells (PSCs). However, most SAM molecules are amphiphilic in nature and tend to form micelles in the commonly used alcoholic processing solvents. This introduces an extra energetic barrier to disassemble the micelles during the binding of SAM molecules on the substrate surface, limiting the formation of a compact SAM. To alleviate this problem for achieving optimal SAM growth, a co-solvent strategy to disassemble the micelles of carbazole-based SAM molecules in the processing solution is developed. This effectively increases the critical micelle concentration to be above the processing concentration and enhances the reactivity of the phosphonic acid anchoring group to allow densely packed SAMs to be formed on indium tin oxide. Consequently, the PSCs derived from using MeO-2PACz, 2PACz, and CbzNaph SAM HSLs show universally improved performance, with the CbzNaph SAM-derived device achieving a champion efficiency of 24.98% and improved stability.
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