Solvothermal synthesis and photocatalytic activity of metal-organic framework materials based on bismuth and trimesic acid
We synthesized metal-organic framework materials based on bismuth and trimesic acid (Bi-BTC) by the solvothermal method using a mixed solvent of N,N-dimethylformamide (DMF) and methanol (MeOH) at different volume ratios. The results have shown that the presence of MeOH ensured the effective Bi-BTC f...
Gespeichert in:
Veröffentlicht in: | Sustainable chemistry and pharmacy 2021-05, Vol.20, p.100385, Article 100385 |
---|---|
Hauptverfasser: | , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
Zusammenfassung: | We synthesized metal-organic framework materials based on bismuth and trimesic acid (Bi-BTC) by the solvothermal method using a mixed solvent of N,N-dimethylformamide (DMF) and methanol (MeOH) at different volume ratios. The results have shown that the presence of MeOH ensured the effective Bi-BTC formation in the DMF environment, meaning that the pure DMF environment was inactive for Bi-BTC formation. The properties of Bi-BTC, such as size and porosity, varied in response to the change of synthetic solvent, resulting in a difference in the photocatalytic properties of the material. The change in the material structure under the influence of different solvents leads to a change in light absorption properties and thus affects their photocatalytic mechanism. Our study contributes a new insight to improve the photocatalytic activity of Bi-BTC.
[Display omitted]
•Metal-Organic Framework based on bismuth and trimesic acid (Bi-BTC) was synthesized by the solvothermal method.•Bi-BTC-DMF/MeOH synthesized using a mixture of DMF and MeOH showed a high specific surface area.•Bi-BTC-DMF/MeOH showed excellent photocatalytic activity with a rate constant of 29.3 × 10−3 min−1.•The reaction mechanism of the rhodamine B photodegradation process over Bi-BTC-DMF/MeOH was also investigated. |
---|---|
ISSN: | 2352-5541 2352-5541 |
DOI: | 10.1016/j.scp.2021.100385 |