Calcium single atoms stabilized by nitrogen coordination in metal–organic frameworks as efficient solid base catalysts

A new single-atom solid base catalyst, Ca1/UiO-67-BPY, is fabricated, in which Ca atoms are immobilized onto N-rich metal–organic framework UiO-67-BPY at room temperature. [Display omitted] Considerable attention has been paid to the preparation of single-atom solid base catalysts (SASBCs) owing to...

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Veröffentlicht in:Journal of colloid and interface science 2025-01, Vol.678 (Pt B), p.88-94
Hauptverfasser: Peng, Song-Song, Liu, Sai, Shao, Xiang-Bin, Zhang, Kai, Liu, Yang, Wang, Yang, Tan, Peng, Yan, Juntao, Sun, Lin-Bing
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Sprache:eng
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Zusammenfassung:A new single-atom solid base catalyst, Ca1/UiO-67-BPY, is fabricated, in which Ca atoms are immobilized onto N-rich metal–organic framework UiO-67-BPY at room temperature. [Display omitted] Considerable attention has been paid to the preparation of single-atom solid base catalysts (SASBCs) owing to their high activity and maximized utilization of basic sites. At present, the reported fabrication methods of SASBCs, such as two-step reduction strategy and sublimation capture strategy, require high temperature. Such a high activation temperature is easy to cause the sublimation loss of alkali or alkaline earth metal atoms and destructive to the support structure. Herein, a new SASBC, Ca1/UiO-67-BPY, is fabricated, in which the alkaline earth metal Ca sites are immobilized onto N-rich metal–organic framework UiO-67-BPY at room temperature. The results show that the atomic configuration of Ca single atoms is coordinated by two N atoms in the framework. The obtained Ca SASBC possesses ordered structure and exhibits high product yield of 87.2% in the Knoevenagel reaction between benzaldehyde and malononitrile. Furthermore, thanks to the Ca single atoms sites anchored on UiO-67-BPY, the Ca1/UiO-67-BPY catalyst also shows good stability during cycles. This work might offer new insight in designing SASBCs for different base-catalyzed reactions.
ISSN:0021-9797
1095-7103
1095-7103
DOI:10.1016/j.jcis.2024.09.019