Fabrication of a two-dimensional bi-lanthanide metal-organic framework as a ratiometric fluorescent sensor based on energy competition

镧系元素 化学 金属有机骨架 荧光 发光 双金属片 带隙 吸收(声学) 水溶液中的金属离子 离子 纳米技术 金属 物理化学 光电子学 材料科学 有机化学 复合材料 吸附 物理 量子力学
作者
Yingying Li,Fang Wang,Maosheng Liang,Mengyu Sun,Lian Xia,Fengli Qu
出处
期刊:Talanta [Elsevier BV]
卷期号:278: 126456-126456 被引量:18
标识
DOI:10.1016/j.talanta.2024.126456
摘要

Bimetallic lanthanide metal-organic frameworks (bi-Ln-MOFs) exhibit great appeal for ratiometric luminescent sensors due to their unique advantages. Specially, the low-lying energy of the empty 4f band of Ce4+ ions benefits Ce-MOFs with robust and broad fluorescent emission. Therefore, constructing ratiometric sensors based on Ce-MOFs is of significance but remains a challenge. Here, a two-dimensional (2D) bi-Ln-MOF is fabricated using Eu3+/Ce4+ and 5-boronoisophthalic acid (5-bop) via a crystal phase transformation strategy to construct a ratiometric luminescent Hg2+ sensor. Due to the lower energy gap of Ce4+ compared to Eu3+ and the corresponding stronger energy-absorption ability, the Ce4+ in bi-Ln-MOF shows a stronger and broader fluorescent emission than that of Eu3+. The substitution of the boric acid group in the bi-Ln-MOF by Hg2+ amplifies the difference between the two lanthanide ions. Therefore, the fluorescence intensity of Ce4+ increases whereas that of Eu3+ decreases accordingly, a behavior distinct from individual Eu-MOF or Ce-MOF performance. This novel bi-Ln-MOF sensor not only achieves a wide linear response range from 0.5 to 120 μM with a low detection limit of 167 nM for Hg2+, but also demonstrates exceptional selectivity and stability. The intriguing sensing mechanism of energy competition and the novel synthesis approach for 2D bi-Ln-MOF are anticipated to broaden the application possibilities of bi-Ln-MOFs for designing ratiometric sensors.
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