Issue 33, 2022

Defect engineering and spilt-over hydrogen in Pt/(WO3–TH2) for selective hydrogenation of C[double bond, length as m-dash]O bonds

Abstract

Defect engineering studies on heterogeneous catalysts are of great scientific significance for the C[double bond, length as m-dash]O activation and adsorption configuration modulation in C[double bond, length as m-dash]O bond-selective hydrogenation reactions. Herein, we report the selective hydrogenation of cinnamaldehyde to cinnamyl alcohol over Pt catalysts supported on pre-reduced WOx. The as-prepared Pt/(WO3–300H2) catalyst displays an excellent performance and gives 93.4% selectivity with 91.1% conversion at 100 °C. The pre-treatment of the support causes generation of defect sites (oxygen vacancies), which facilitates the reduction and dispersion of Pt and the formation of spilt-over H species. The cinnamaldehyde molecules are preferably adsorbed on the defect sites in the metal support interfacial area and then transform to cinnamyl alcohol with the assistance of spilt-over H. The present work provides useful knowledge for surface defect engineering of catalysts and the design of efficient catalytic materials for C[double bond, length as m-dash]O activation.

Graphical abstract: Defect engineering and spilt-over hydrogen in Pt/(WO3–TH2) for selective hydrogenation of C [[double bond, length as m-dash]] O bonds

Supplementary files

Article information

Article type
Paper
Submitted
19 May 2022
Accepted
22 Jul 2022
First published
22 Jul 2022

New J. Chem., 2022,46, 15950-15958

Defect engineering and spilt-over hydrogen in Pt/(WO3–TH2) for selective hydrogenation of C[double bond, length as m-dash]O bonds

Y. Liu, X. Wang, C. Zhang, Q. Xu, L. Dang, X. Zhao, H. Tan, Y. Li and F. Zhao, New J. Chem., 2022, 46, 15950 DOI: 10.1039/D2NJ02497G

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements