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Constructing a Z-scheme Fe-MOF-based heterostructure for visible-light-driven oxidation of aromatic alcohol in ambient air.

Authors :
Zhang, Lu
Qiu, Jianhao
Xia, Guanglu
Dai, Dingliang
Zhong, Xiang
Yao, Jianfeng
Source :
Journal of Materials Science & Technology; Mar2023, Vol. 138, p214-220, 7p
Publication Year :
2023

Abstract

• Spindle-shaped MIL-53(Fe)-NH 2 @ZnIn 2 S 4 photocatalysts were facilely developed. • A Z-scheme heterostructure is assuredly formed between ZnIn 2 S 4 and MIL-53-NH 2. • The photocatalytic BA conversion can be notably enhanced in ambient air. • The benzaldehyde production rate can surpass most studies in air, O 2 or inert gas. Photocatalytic oxidation of aromatic alcohol into aromatic aldehyde using O 2 has received huge attention, while the reaction that occurred in ambient air is rarely studied but follows the green-chemistry principles. Herein, spindle-shaped MIL-53(Fe)-NH 2 @ZnIn 2 S 4 photocatalysts with a Z-scheme heterostructure were facilely developed for photocatalytic oxidation of aromatic alcohol in air under visible light. The benzyl alcohol conversion can be notably enhanced to 73% over the optimal MIL-53-NH 2 @ZnIn 2 S 4 sample with a benzaldehyde production rate of 1825 μmol g<superscript>–1</superscript> h<superscript>–1</superscript>. However, in the O 2 atmosphere, the benzyl alcohol conversion is only 56%, indicating that O 2 is not required and has an adverse effect on the reaction. The hierarchical structure and Z-scheme heterojunction of MIL-53-NH 2 @ZnIn 2 S 4 impart an efficient separation and strong redox abilities of photo-induced electrons and holes, which are responsible for the impressive photocatalytic performance. This study could motivate the ingenious design of Z-scheme heterostructures for green organic conversion based on MOFs. [Display omitted] [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
10050302
Volume :
138
Database :
Supplemental Index
Journal :
Journal of Materials Science & Technology
Publication Type :
Periodical
Accession number :
160330450
Full Text :
https://doi.org/10.1016/j.jmst.2022.08.009