成核
结晶
材料科学
能量转换效率
化学工程
降水
甲脒
同步
串联
相(物质)
钙钛矿(结构)
共晶体系
格子(音乐)
晶体生长
同种类的
化学物理
硫氰酸盐
能量转换
纳米技术
光电子学
饱和(图论)
卤化物
作者
Bin Huang,Likai Zheng,Ruixiong Hu,Yimin Xuan
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2026-04-17
卷期号:11 (5): 4055-4066
被引量:2
标识
DOI:10.1021/acsenergylett.6c00617
摘要
Methylammonium-free (MA-free) tin–lead perovskites are essential for durable all-perovskite tandem solar cells (APTSCs), yet the lower activation energy of Sn-based phases triggers a premature nucleation driving force, leading to detrimental Sn-rich phase precipitation and significant lattice strain. Herein, we introduce rubidium thiocyanate (RbSCN) as a multifunctional regulator to orchestrate the crystallization dynamics and strain evolution. SCN – selectively coordinates with Sn 2+, retarding premature Sn-rich phase precipitation and synchronizing the growth rates of Sn/Pb-mixed phases. Simultaneously, Rb + mitigates local lattice distortion, yielding structurally homogeneous films with minimized nonradiative recombination. Consequently, the optimized MA-free Sn–Pb device achieves a 22.92% power conversion efficiency (PCE) and exhibits enhanced operational stability. Integrating this into monolithic APTSCs realizes a PCE of 28.77% (TÜV-certified 28.53%). Notably, the V OC × FF product represents the highest value reported for MA-free APTSCs, highlighting the efficacy of synchronized crystallization in unleashing the potential of narrow-bandgap perovskites.
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