钙钛矿(结构)
卤化物
锡酸盐
结晶
成核
碘化物
材料科学
带隙
化学工程
化学
结晶学
无机化学
光电子学
冶金
有机化学
工程类
锌
作者
Weiqing Chen,Shun Zhou,Hongsen Cui,Weiwei Meng,Hongling Guan,Guojun Zeng,Yansong Ge,Sengke Cheng,Zhenhua Yu,Dexin Pu,Lishuai Huang,Jin Zhou,Guoyi Chen,Guang Li,Hongyi Fang,Zhiqiu Yu,Hai Zhou,Guojia Fang,Weijun Ke
标识
DOI:10.1038/s41467-025-57195-w
摘要
Abstract Precise control over halide perovskite crystallization is pivotal for realizing efficient solar cells. Here, we introduce a strategy utilizing in-situ-formed oxide-based ABX 3 -structured seeds to regulate perovskite crystallization and growth. Introducing potassium stannate into perovskite precursors triggers a spontaneous reaction with lead iodide, producing potassium iodide and lead stannate. Potassium iodide effectively passivates defects, while PbSnO 3 (ABX 3 -structured), exhibiting a 98% lattice match, acts as a template and seed. This approach facilitates pre-nucleation cluster formation, preferential grain orientation, and the elimination of intermediate-phase processes in perovskite films. Incorporating potassium stannate into both the perovskite precursors and the buried hole transport layers enables single-junction 1.25 eV-bandgap Sn-Pb perovskite solar cells to achieve a steady-state efficiency of 23.12% and enhanced stability. Furthermore, all-perovskite tandem devices yield efficiencies of 28.12% (two-terminal) and 28.81% (four-terminal). This versatile templating method also boosts the performance of 1.77 eV and 1.54 eV-bandgap cells, underscoring its broad applicability.
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