Dissolution-Recrystallization: A Novel Mechanism for Fluorochromic Detection of Th 4+ Using Color-Tunable Luminescent Metal-Organic Frameworks
Thorium, a predominant actinide in the Earth's crust, presents significant environmental and health risks due to its radioactive nature. These risks are particularly pronounced during the mining and processing of monazite for rare earth elements (REEs), which contain substantial thorium concent...
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Veröffentlicht in: | Angewandte Chemie International Edition 2024-11, Vol.63 (46), p.e202410453 |
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Sprache: | eng |
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Zusammenfassung: | Thorium, a predominant actinide in the Earth's crust, presents significant environmental and health risks due to its radioactive nature. These risks are particularly pronounced during the mining and processing of monazite for rare earth elements (REEs), which contain substantial thorium concentrations. Current instrumental analysis methods for thorium, offer high accuracy but require laborious sample preparations and expensive instruments, making them unsuitable for on-site analysis. Herein, we present a class of color-tunable luminescent lanthanide-based metal-organic frameworks (Ln-MOFs) as fluorochromic sensors for Th
cations. Utilizing a heterobimetallic Eu
/Tb
doping strategy, the luminescence colors of Eu
Tb
-BDC-OH can be finely tuned from red, to orange, and to green. More intriguingly, the higher Lewis acidity of Th
facilitates the transformation of Eu
Tb
-BDC-OH into a UiO-type Th-MOF via a dissolution-recrystallization mechanism. This process results in a gradual reduction of characteristic Ln
emissions and the emergence of blue color ligand-based fluorescence, thereby leading to selective fluorochromic responses with increasing Th
concentrations and enabling visible detection of Th
cations. Additionally, a custom-built portable optoelectronic device is fabricated, which directly converts luminescence colors into red-green-blue (RGB) values. This device enables easy quantification of Th
concentrations without the need for complex instrumentation. |
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ISSN: | 1433-7851 1521-3773 |
DOI: | 10.1002/anie.202410453 |