化学
结晶度
钙钛矿(结构)
光电子学
结晶
氯化铅
纳米尺度
光伏
氯化物
发光
动力学
相(物质)
晶界
同质性(统计学)
氯
能量转换效率
光伏系统
聚合物
纳米技术
光致发光
化学工程
作者
Junke Wang,Shuaifeng Hu,Xinyu Gu,Minh Anh Truong,Yi Yang,Cheng Liu,Gunnar Kusch,Zhongcheng Yuan,Manuel Kober‐Czerny,Zuhong Zhang,Zhenhuang Su,Kyohei Nakano,Akash Dasgupta,X. Zhang,Xinyi Shen,Nobutaka Shioya,Noriko Kurose,Daichi Shirakura,Zaiwei Wang,Wei Zhou
摘要
Improving the bulk quality of perovskite films is critical for achieving higher-performance photovoltaic devices. Chloride-containing additives, including lead chloride (PbCl2) and methylammonium chloride (MACl)─standard additives widely adopted in perovskite photovoltaics─are effective for controlling crystallization kinetics and grain morphology. However, the distinct impacts of different forms of chloride additives on nanoscale phase uniformity and luminescence homogeneity remain underexplored. Here, we provide new insights into how the choice and combination of chloride additives influence phase transitions and spatially uniform carrier dynamics within perovskite films. We demonstrate that strategically combining MACl and PbCl2 improves crystallinity and optoelectronic uniformity across dimensions spanning micrometers to millimeters. Leveraging these findings, we fabricated inverted (p-i-n) perovskite solar cells achieving certified quasi-steady-state efficiencies of 26.4% and 24.5% at device areas of 0.05 and 1 cm2, respectively. Furthermore, these devices exhibit robust operational stability, retaining 88% of their initial performance after 1200 h of continuous maximum power point tracking at elevated temperatures (65 °C) under simulated AM1.5G illumination. Our results elucidate the mechanistic differences between chloride additive forms, providing a viable strategy for advancing large-area, high-efficiency, and thermally stable perovskite photovoltaics.
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