结晶
制作
成核
材料科学
退火(玻璃)
相对湿度
能量转换效率
钙钛矿(结构)
化学工程
纳米技术
湿度
相(物质)
光伏系统
光电子学
涂层
作者
Weideren Dai,Jie Li,Yanzhuo Gou,Jiaqi Zhang,Zexun Pan,Xianglong Li,Haojun Hu,S. Q. Wang,Tao Mei,Xianbao Wang,Chao Chen,Qidong Tai,Jingbi You
标识
DOI:10.1038/s41467-026-69687-4
摘要
The intrinsic phase instability of CsPbI3 perovskites necessitates stringent fabrication conditions, significantly hindering the practical deployment. In the DMA-mediated CsPbI3 nucleation system, the Cs+/DMA+ ion exchange critically governs the resulting film quality. Here, we employ a moisture-responsive crystallization strategy utilizing propyltriethoxysilane (PTES) to deposite CsPbI3 under ambient air with high humidity (55%). We demonstrate that the siloxane groups can capture DMA+ in the intermediate DMAPbI3, facilitating DMA+ extraction and Cs+ incorporation, thereby accelerating crystallization kinetics. This approach enables CsPbI3 PSCs to achieve a power conversion efficiency (PCE) of 21.00% with an impressive fill factor (FF) of 86.1% while processing perovskite under relative humidity (RH) of 55%. Higher PCEs of 21.85% and 22.60% (certified 22.02%) were achieved for devices fabricated at a lower RH of 25% and for films spin-coated under an N2 atmosphere followed by annealing in ambient air, respectively. Furthermore, PTES-treated devices exhibit excellent operational stability under ambient conditions. CsPbI₃ perovskites face severe phase instability, limiting practical fabrication. The authors introduce a PTES-based moisture-responsive strategy enabling ambient processing and achieving up to 22.6% efficiency with improved stability.
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