卤化物
化学物理
串联
同种类的
光致发光
材料科学
相(物质)
离子
再分配(选举)
动能
化学
混合(物理)
纳米技术
结构稳定性
分子动力学
光伏系统
作者
Fuyi Zhou,Haimeng Xin,Jinghan Zhu,Yueran Xiang,Zhongkang Han,Deren Yang,Zhenyi Ni
标识
DOI:10.1021/acsenergylett.6c01537
摘要
Wide-bandgap (WBG) mixed-halide perovskites are highly promising for tandem photovoltaic applications, yet their operational stability remains limited by ion-migration-driven phase segregation. Existing mechanistic understandings on the ion migration dynamics largely rely on idealized homogeneous halide distribution models, overlooking the influence of intrinsic halide concentration gradients. Here, we elucidate the dynamics of halide-gradient-driven ion migration in WBG perovskites, uncovering a pronounced kinetic inversion in the migration energy barriers between I − and Br − that depends on local halide stoichiometry. Driven by the coupled effects of concentration gradients and spatially heterogeneous migration barriers, halide redistribution fundamentally deviates from classical homogenization, culminating in a distinctive “sandwich-like” segregated architecture with I-rich regions at both interfaces and Br-rich domains in the bulk, as directly validated by cross-sectional photoluminescence spectral mapping. Our findings establish a new mechanistic framework for gradient-driven phase segregation and provide actionable insights for designing intrinsically stable WBG perovskites for high-performance tandem photovoltaics.
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