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...
Gespeichert in:
Veröffentlicht in: | Journal of colloid and interface science 2025-01, Vol.678 (Pt B), p.88-94 |
---|---|
Hauptverfasser: | , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
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 |