材料科学
发光
钙钛矿(结构)
甲醇
纳米技术
光电子学
化学工程
有机化学
化学
工程类
作者
Xiu‐Xian Guo,Jing‐Hua Chen,Jianbin Luo,Jun‐Hua Wei,Zhizhong Zhang,Zi‐Lin He,Qing‐Peng Peng,Dai‐Bin Kuang
标识
DOI:10.1002/adom.202400681
摘要
Abstract Stimuli‐responsive luminescent materials have attracted much research attention due to their wide application potential in various fields. Typically, the family of hydrated double perovskite A 2 M III X 5 ·H 2 O shows unique emission color transformation between hydrated and dehydrated complexes, highlighting the application potential in advanced anti‐counterfeiting. Herein, two zero‐dimensional perovskites of Cs 2 YbCl 5 ·H 2 O and Cs 3 YbCl 6 , are reported and broad‐band self‐trapped exciton recombination emission can be realized via external Sb 3+ doping. Intriguingly, the Cs 2 YbCl 5 ·H 2 O can be transformed to the dehydrated counterpart of Cs 3 YbCl 6 through a facile methanol treatment at room temperature, leading to the emission color transformation from yellow to green. Notably, the green‐emissive Cs 3 YbCl 6 :Sb 3+ delivers a high photoluminescence quantum yield of 67.3%. Leveraging the advantages of obvious methanol‐induced emission color transformation between Cs 2 YbCl 5 ·H 2 O and Cs 3 YbCl 6 at room temperature, Cs 2 YbCl 5 ·H 2 O can be used in the field of high‐security‐level anti‐counterfeiting.
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