Xiaohong Zhang, Siyuan Lin, Changfu Xu, Haiyan Shi, Kai Li, Pan Zhou, Pengbo Lyu, Lizhong Sun
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引用次数: 0
Abstract
Structural phase evolution is among the most powerful tools for tuning material properties, enabling advancements in catalysis, dielectrics, optoelectronics, and photoluminescence. Such an evolution can significantly enhance the near-infrared (NIR) emission properties of Cr3+-doped phosphors. Herein, we present, to the best of our knowledge, the first observation of lithiation-induced continuous structural phase evolution in ZnTa2O6 phosphors, driven by Li+ incorporation. This evolution proceeds systematically from orthorhombic ZnTa2O6 (Pbcn) to tetragonal ZnTa2O6 (P42/mnm) and ultimately to trigonal (Li0.5Zn0.5)TaO3 (R3c) as the Li+ content increases. When doped with Cr3+, the NIR emission peak exhibits a progressive blue shift, moving from 949 to 885 nm and eventually to 862 nm, in tandem with the phase evolution. This phase evolution also yields significant enhancements in photoluminescent intensity, internal quantum yield (IQY), and photoluminescence thermal stability. Our findings establish a new paradigm for designing highly efficient ultra-broadband NIR phosphors and offer a foundation for developing tantalate-based materials with versatile functionalities, including improved dielectric properties.
期刊介绍:
Inorganic Chemistry publishes fundamental studies in all phases of inorganic chemistry. Coverage includes experimental and theoretical reports on quantitative studies of structure and thermodynamics, kinetics, mechanisms of inorganic reactions, bioinorganic chemistry, and relevant aspects of organometallic chemistry, solid-state phenomena, and chemical bonding theory. Emphasis is placed on the synthesis, structure, thermodynamics, reactivity, spectroscopy, and bonding properties of significant new and known compounds.