兴奋剂
加密
材料科学
纳米技术
计算机科学
光电子学
计算机安全
作者
Xiaolong Dong,Xin Zhao,Yuhang Zhang,Min Hu,Lifan Shen,Edwin Yue‐Bun Pun,Hai Lin
标识
DOI:10.1002/lpor.202402120
摘要
Abstract Driven by the escalating demand for cutting‐edge materials in interactive encryption and customized display, the optimization of excitonic coupling mechanisms in perovskite‐based luminescent systems has emerged as a pivotal focus in advanced materials research. Inspired by synergistic doping (SD), a photoswitchable energy transfer channel is realized utilizing the UV‐responsive Cs 2 NaInCl 6 : Sb 3+ ‐Ho 3+ (CNIC: Sb‐Ho) phosphor. Benefiting from the self‐trapped exciton of Sb 3+ , the visible blue luminescence of Ho 3+ achieves excitation reconstruction through SD, with a sensitization coefficient from Sb 3+ to Ho 3+ in CNIC reaching two orders of magnitude. Notably, CNIC: Sb‐Ho quantum dot is embedded into polyacrylonitrile (PAN) and polymethyl methacrylate (PMMA) fibers, respectively, and distinct color coordinate channels are created by altering the doping concentration and fiber matrix, thereby enabling the personalization and the customization of the desired colors with enhanced precision. Furthermore, excellent read‐in performance under UV irradiation is achieved by screen‐printing CNIC: Sb‐Ho microcrystal on nanofibers and combining it with ACSII code, which endows nanofibers with UV‐induced controllable shape programming behavior for interactive multidimensional information encryption. This work establishes an enhanced visual interaction framework through effectively integrating perovskite fluorescence tunability and nanofiber adaptive structures, thus opening new possibilities for the smart application of next‐generation optical encryption technology.
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