Highly Stable Pt-Co Bimetallic Catalysts Prepared by Atomic Layer Deposition for Selective Hydrogenation of Cinnamaldehyde
Abstract
Pt-Co bimetallic catalysts were deposited on γ-Al2O3 nanoparticles by atomic layer deposition (ALD) and were used for selective hydrogenation of cinnamaldehyde (CAL) to cinnamyl alcohol (COL). High resolution transmission electron microscopy, hydrogen temperature-programmed reduction, X-ray diffraction, and X-ray photoelectron spectroscopy were used to identify the strong interaction between Pt and Co. The obtained catalysts with an optimal Pt/Co ratio achieved a COL selectivity of 81.2% with a CAL conversion of 95.2% under mild conditions (i.e., 10 bar H2 and 80 °C). During the CAL hydrogenation, the addition of Co on Pt significantly improved the activity and selectivity due to the synergetic effects of Pt-Co bimetallic catalysts, resulted from the transfer of electrons from Co to Pt, which can stabilize the carbonyl groups. The obtained Pt-Co bimetallic catalysts also showed excellent stability due to the strong interaction between the metal nanoparticles and the alumina support. Negligible losses in the activity and selectivity were observed during the recycling experiments, showing the potential for practical applications.
Recommended Citation
K. Wang et al., "Highly Stable Pt-Co Bimetallic Catalysts Prepared by Atomic Layer Deposition for Selective Hydrogenation of Cinnamaldehyde," Nanotechnology, vol. 33, no. 21, article no. 215602, IOP Publishing, Mar 2022.
The definitive version is available at https://doi.org/10.1088/1361-6528/ac5540
Department(s)
Chemical and Biochemical Engineering
Keywords and Phrases
ALD; Pt-Co Bimetallic Catalysts; Selective Hydrogenation; Stability
International Standard Serial Number (ISSN)
1361-6528; 0957-4484
Document Type
Article - Journal
Document Version
Citation
File Type
text
Language(s)
English
Rights
© 2022 IOP Publishing, All rights reserved.
Publication Date
04 Mar 2022
PubMed ID
35168219
Comments
This work was supported by the National Science Foundation grant NSF 1803812.