Affiliation:
1. College of Chemistry Sichuan University Chengdu 610065 P. R. China
2. The State Key Laboratory of Luminescent Materials and Devices School of Materials Science and Engineering South China University of Technology Guangzhou 510641 P. R. China
3. College of Chemistry and Materials Science Fujian Key Laboratory of Polymer Materials Fujian Normal University Fuzhou 350007 P. R. China
Abstract
AbstractAchieving tunable emissions spanning the spectrum, from blue to near‐infrared (NIR) light, within a single component is a formidable challenge with significant implication, particularly in tailoring multicolor luminescence for anti‐counterfeiting purposes. In this study, we demonstrate a broad spectrum of emissions, covering blue to red and extending into NIR light in [BPy]2CdX4 : xSb3+ (BPy=Butylpyridinium; X=Cl, Br; x=0 to 0.08) through precise multisite structural fine‐tuning. Notably, the multicolor emissions from [BPy]2CdBr4 : Sb3+ manifest a distinctive pattern, transitioning from blue to yellow in tandem with the host [BPy]2CdBr4 and further extending from yellow to NIR with its homologous [BPy]2CdCl4 : Sb3+, resulting in the simultaneous presence of intersecting and independent emission colors. Detailed modulation of chemical composition enables partial luminescence switching, facilitating the creation of diverse patterns with multicolor luminescence by employing [BPy]2CdX4 : xSb3+ as phosphors. This study for the first time successfully implements several groups of tunable emission colors in a single matrix via multisite fine‐tuning. Such an effective strategy not only develops the specific relationships between tunable emissions and adjustable compositions, but also introduces a cost‐effective and straightforward approach to achieving unique, high‐level, plentiful‐color and multiple‐information‐storage labels for advanced anti‐counterfeiting applications.
Funder
Excellent Young Scientists Fund
National Natural Science Foundation of China
Cited by
8 articles.
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