Guest‐Dependent Stimuli‐Responsive Photoluminescence in 0D Antimony Chlorides for Anticounterfeiting and Encryption Applications
Source abstract
Abstract
Abstract 0D lead‐free metal halides with stimuli‐responsive photoluminescence (PL) have attracted great attention as promising smart materials for advanced anticounterfeiting and information encryption. However, designing high‐performance stimuli‐responsive metal halides remains a challenge. Herein, a solvent guest tuning strategy to develop stimuli‐responsive 0D metal halides is proposed. Three novel highly yellow‐emissive host‐guest systems, TMA2SbCl5·X (TMA: (CH3)4N+, X = DMSO, DMF, and MeCN) are synthesized. Under heat stimuli, TMA2SbCl5·X (X = DMSO and DMF) exhibits PL on‐off switching, while TMA2SbCl5·MeCN shows PL color change from yellow to orange, due to structural phase transitions. Particularly, TMA2SbCl5·DMSO and TMA2SbCl5·MeCN demonstrate a fast response within 50 s at temperatures above 353 K. Detailed in situ XRD diffraction study unveils the role of guest solvent molecules in the regulation of structural phase transitions. For the first time, it is found that the host‐guest systems possess a guest‐dependent structural evolution that results in a different PL response to heat stimuli. In addition, moister can also trigger structural phase transition and induce PL on‐off switching. The remarkable stimuli response performance makes these hybrids promising for anticounterfeiting and encryption applications. These findings provide new insights for the development of stimuli‐responsive lead‐free metal halide materials.
Source: crossref · Quality: baseline
Research context
OpenAlex topics: Perovskite Materials and Applications · Nanocluster Synthesis and Applications · 2D Materials and Applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Institute of Frontier Chemistry School of Chemistry and Chemical Engineering Shandong University Qingdao 266237 P.R. China
State Key Laboratory of Molecular Reaction Dynamics Dalian Institute of Chemical Physics Chinese Academy of Science Dalian 116023 P.R. China
SDU‐ANU Joint Science College Shandong University Weihai 264209 P. R. China
Nano‐Science Center & Department of Chemistry University of Copenhagen Universitetsparken 5 Copenhagen 2100 Denmark
Funding
National Natural Science Foundation of China
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