光子上转换
纳米晶
材料科学
能量转移
紫外线
荧光粉
兴奋剂
发光
光电子学
离子
纳米技术
化学
化学物理
有机化学
作者
Wen Zhang,Wei Zheng,Ping Huang,Dengfeng Yang,Zhiqing Shao,Wei Zhang,Hao Zhang,Zhihui Xie,Jin Xu,Xueyuan Chen
标识
DOI:10.1038/s41467-025-58901-4
摘要
Abstract Yb 3+ /Er 3+ activated upconversion (UC) materials have been widely applied in many advanced technologies owing to their high UC efficiency in the visible region. However, it is challenging to achieve efficient ultraviolet (UV) UC luminescence (UCL) in Yb 3+ /Er 3+ system, due to the dense energy levels of Er 3+ that impose deleterious nonradiative relaxation. Herein, we report a strategy to liberate the UV-UCL of Er 3+ based on the confined energy transfer in Yb 3+ /Er 3+ co-doped 0D Rb 3 InCl 6 with a low phonon energy and a large interionic distance. This facilitates the population of Er 3+ at the 4 G 11/2 state, which yields intense upconverted UV emission at 384 nm, with a much higher UV-to-green ratio ( I 384 / I 554 = 0.864) than that of traditional UC materials ( < 0.1). By leveraging the intense upconverted UV emission of Er 3+ , we demonstrate the application of Rb 3 InCl 6 :Yb 3+ /Er 3+ nanocrystals as a NIR-to-UV transducer for NIR-triggered anion exchange of CsPbX 3 perovskite nanocrystals with high efficiency and good controllability. These findings offer an approach for the exploration of novel UC materials via energy transfer and crystal lattice engineering towards versatile applications.
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