光子上转换
异质结
材料科学
光电子学
外延
制作
能量转移
光子
纳米技术
发光
纳米颗粒
图层(电子)
激光器
能量(信号处理)
活动层
受激发射
结晶
能量转换
高能
离子键合
光子能量
纳米复合材料
作者
Fen Li,Zhiqing Wang,Yaxin Li,Wanying Zhang,Song Wang,Yingwei Wang,Jianrong Zeng,Yi Wei,Dong Tu,Zhijie Ju,Renren Deng,Keqiang Chen,Guo-Gang Li,Fen Li,Zhiqing Wang,Yaxin Li,Wanying Zhang,Song Wang,Yingwei Wang,Jianrong Zeng
标识
DOI:10.1002/anie.202521996
摘要
Abstract Hybrid heterojunctions integrating lanthanide‐doped upconversion nanoparticles (UCNPs) and lead‐halide perovskites (LHPs) offer compelling opportunities for multimodal luminescence and tailored photon conversion. However, the synthesis of well‐defined UCNP/LHP heterostructures is hindered by the rapid crystallization kinetics and ionic character of perovskites, while the energy transfer mechanisms—particularly the role of LHPs in modulating upconversion—remain poorly understood. Here, we demonstrate a thermodynamics‐controlled epitaxial growth strategy that enables the fabrication of high‐quality NaYF 4 :Yb,Tm/Cs 4 PbBr 6 heterostructures with tunable architecture—from core/shell to UCNP‐in‐LHP solids. Crucially, the Cs 4 PbBr 6 layer acts not merely as a passive energy acceptor, but as a functional sub‐energy level that facilitates back energy transfer to Tm 3+ and redirects its excited‐state population. This coherent energy recycling enables broadly tunable upconversion emission across the entire visible spectrum. Our findings provide a robust route to high‐quality UCNP/LHP heterostructures and establish LHPs as active participants in the engineering of upconversion pathways.
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