Back to Search Start Over

Dissolution‐Recrystallization: A Novel Mechanism for Fluorochromic Detection of Th4+ Using Color‐Tunable Luminescent Metal–Organic Frameworks.

Authors :
Cui, Yunyi
Lu, Huangjie
Hou, Huiliang
Bai, Yaoyao
Yang, Junpu
Li, Yarui
Qiu, Jie
Wang, Shuao
Lin, Jian
Source :
Angewandte Chemie; 11/11/2024, Vol. 136 Issue 46, p1-9, 9p
Publication Year :
2024

Abstract

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 Th4+ cations. Utilizing a heterobimetallic Eu3+/Tb3+ doping strategy, the luminescence colors of EuxTb1‐x‐BDC‐OH can be finely tuned from red, to orange, and to green. More intriguingly, the higher Lewis acidity of Th4+ facilitates the transformation of EuxTb1‐x‐BDC‐OH into a UiO‐type Th‐MOF via a dissolution‐recrystallization mechanism. This process results in a gradual reduction of characteristic Ln3+ emissions and the emergence of blue color ligand‐based fluorescence, thereby leading to selective fluorochromic responses with increasing Th4+ concentrations and enabling visible detection of Th4+ 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 Th4+ concentrations without the need for complex instrumentation. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00448249
Volume :
136
Issue :
46
Database :
Complementary Index
Journal :
Angewandte Chemie
Publication Type :
Academic Journal
Accession number :
180657184
Full Text :
https://doi.org/10.1002/ange.202410453