材料科学
光致发光
激发态
光电子学
紫外线
发光
原子物理学
物理
作者
Hao Suo,Nan Wang,Yu Zhang,Xin Zhang,Jinmeng Xiang,Xiaojia Wang,Guansheng Xing,Dongxu Guo,Jiwen Chang,Yu Wang,Panlai Li,Zhijun Wang,Yuhai Zhang,Bing Chen,Shuzhou Li,Chongfeng Guo,Feng Wang
标识
DOI:10.1038/s41377-024-01689-7
摘要
Abstract Low-dimensional lead-free metal halide perovskites are highly attractive for cutting-edge optoelectronic applications. Herein, we report a class of scandium-based double perovskite crystals comprising antimony dopants that can generate multiexcitonic emissions in the ultraviolet, blue, and yellow spectral regions. Owing to the zero-dimensional nature of the crystal lattice that minimizes energy crosstalk, different excitonic states in the crystals can be selectively excited by ultraviolet light, X-ray irradiation, and mechanical action, enabling dynamic control of steady/transient-state spectral features by modulating the excitation modes. Remarkably, the transparent crystal exhibits highly efficient white photoluminescence (quantum yield >97%), X-ray excited blue emission with long afterglow (duration >9 h), and high-brightness self-reproducible violet-blue mechanoluminescence. These findings reveal the exceptional capability of low-dimensional perovskite crystals for integrating various excitonic luminescence, offering exciting opportunities for multi-level data encryption and all-in-one authentication technologies.
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