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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Guo et al. (2024) studied this question.
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