Zeolite-confined silver nanoclusters (AgNCs/Zeolite) are highly promising luminescent materials. Nevertheless, the controlled synthesis of AgNCs/Zeolite composites with tunable luminescent responses remains a persistent challenge. In this study, highly luminescent AgNCs/Zeolite composites are developed through the counter-cations engineering strategy via confining AgNCs within the cages of FAUX with Na and Zn as the counter cations (Ag-FAUX(Na/Zn)), which show water-triggered switchable yellow/green tunable-emissive properties with PLQY up to 90% and high tolerance to chemical reduction. Specifically, dehydration of Ag-FAUX(Na/Zn) increases its PLQY from 60% to 90% and shifts the emission peak from 560 to 520 nm, whereas the yellow emission of the sample without Zn (Ag-FAUX(Na/Zn)) is almost completely quenched upon dehydration. The remarkably enhanced luminescence upon dehydration can be tentatively ascribed to the coordination of Zn with framework oxygen (O) of FAUX, thereby preventing AgNCs from direct interaction with O of Ag-FAUX(Na/Zn), and finally forming the stable, tightly confined Ag interacting with nonframework oxygen and zinc atoms simultaneously. The Ag-FAUX(Na/Zn) composites demonstrated exceptional performance in fluorescence detection of trace water in organic solvents, achieving high sensitivity, a low detection limit of 0.015% v/v, rapid response times of less than 0.5 s, and reusability, thereby positioning it as a promising candidate for advanced fluorescence detection applications.
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http://dx.doi.org/10.1021/acs.inorgchem.4c04852 | DOI Listing |
Inorg Chem
March 2025
School of Chemical Engineering and Technology, Hebei University of Technology, GuangRong Dao 8, Hongqiao District, Tianjin 300130, China.
Zeolite-confined silver nanoclusters (AgNCs/Zeolite) are highly promising luminescent materials. Nevertheless, the controlled synthesis of AgNCs/Zeolite composites with tunable luminescent responses remains a persistent challenge. In this study, highly luminescent AgNCs/Zeolite composites are developed through the counter-cations engineering strategy via confining AgNCs within the cages of FAUX with Na and Zn as the counter cations (Ag-FAUX(Na/Zn)), which show water-triggered switchable yellow/green tunable-emissive properties with PLQY up to 90% and high tolerance to chemical reduction.
View Article and Find Full Text PDFInorg Chem
November 2023
National-Local Joint Engineering Laboratory for Energy Conservation in Chemical Process Integration and Resources Utilization, Tianjin Key Laboratory of Chemical Process Safety, School of Chemical Engineering and Technology, Hebei University of Technology, GuangRong Dao 8, Hongqiao District, Tianjin 300130, P. R. China.
Inorg Chem
December 2022
National Co-Innovation Center for Nuclear Waste Disposal and Environmental Safety, Southwest University of Science and Technology, Mianyang 621010, China.
Effective capture of radioactive iodine is highly desirable for decontamination purposes in spent fuel reprocessing. Cu-based adsorbents with a low cost and high chemical affinity for I molecules act as a decent candidate for iodine elimination, but the low utilization and stability remain a significant challenge. Herein, a facile in situ confined synthesis strategy is developed to design and synthesize a copper-encapsulated flaky silicalite-1 (Cu@FSL-1) zeolite with a thickness of ≤300 nm.
View Article and Find Full Text PDFChem Sci
October 2022
Chem&Tech - Molecular Imaging and Photonics, KU Leuven Celestijnenlaan 200F 3001 Leuven Belgium
Zeolite confined silver clusters (AgCLs) have attracted extensive attention due to their remarkable luminescent properties, but the elucidation of the underlying photophysical processes and especially the excited-state dynamics remains a challenge. Herein, we investigate the bright photoluminescence of AgCLs confined in Linde Type A zeolites (LTA) by systematically varying the temperature (298-77 K) and co-cation composition (Li/Na) and examining their respective influence on the steady-state and time-resolved photoluminescence. The observed polychromatic emission of the tetrahedral Ag(HO) clusters ranges from orange to violet and three distinct emitting species are identified, corresponding to three long-lived triplet states populated consecutively and separated by a small energy barrier.
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