钙钛矿(结构)
钝化
单层
材料科学
光伏系统
纳米尺度
偶极子
光伏
纳米技术
光电子学
曲面(拓扑)
薄膜
图层(电子)
化学工程
化学物理
卤化物
离子
化学稳定性
能量转换效率
作者
Dongjiu Zhang,Smail Mostefaoui,Daming Zheng,José Álvarez,Rebeca Lopez-Adams,Jiazhuo Nie,Sergio Vlaic,Yusheng Wang,Baoquan Sun,Philippe Lang,Thierry Pauporté,Lionel Aigouy,Jérôme Aléon,Zhuoying Chen
出处
期刊:ACS Nano
[American Chemical Society]
日期:2026-03-31
卷期号:20 (14): 11294-11305
标识
DOI:10.1021/acsnano.6c00728
摘要
Self-assembled monolayers (SAMs) are widely employed to tune interfacial properties in perovskite solar cells (PSCs), yet they have so far been regarded as strictly two-dimensional surface modifiers. Here, we uncover the three-dimensional (3D) nature of perfluorinated silanol-based SAMs applied onto perovskite films and their impact on both the photovoltaic performance and stability of PSCs. Using high-resolution 3D nanoscale secondary ion mass spectrometry, which directly maps their lateral and vertical distribution, we reveal that these SAMs not only decorate the perovskite surface but also selectively penetrate and anchor at grain-boundary iodine-deficient regions within ∼100 nm of the film. This dual surface-bulk passivation reshapes the defect landscape in perovskite thin films, yielding reduced nonradiative recombination, more favorable interfacial energetics, enhanced photovoltaic performance, and increased environmental stability. Our findings reposition SAMs as volumetric chemical modifiers rather than merely interface dipole layers, highlighting their potential for molecular-level engineering in perovskite optoelectronics.
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