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Article | Open Access

Electrochemical-Method-Induced Strong Metal-Support Interaction in Pt-CNT@SnO2 for CO-Tolerant Hydrogen Oxidation Reaction

Shen-Zhou Lia,#, Zi-Jie Lina,#, Qi-An Chena,#, Zhao Caib, Qing Lia ( )
State Key Laboratory of Materials Processing and Die & Mould Technology, School of Materials Science and Engineering, Huazhong University of Science and Technology, 1037 Luoyu Road, Wuhan 430074, Hubei, China
Faculty of Materials Science and Chemistry, China University of Geosciences (Wuhan), Wuhan 430074, China

# Equal contributions.

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Abstract

Inducing the classic strong metal-support interaction (SMSI) is an effective approach to enhance the performance of supported metal catalysts by encapsulating the metal nanoparticles (NPs) with supports. Conventional thermal reduction method for inducing SMSI processes is often accompanied by undesirable structural evolution of metal NPs. In this study, a mild electrochemical method has been developed as a new approach to induce SMSI, using the cable structured core@shell CNT@SnO2 loaded Pt NPs as a proof of concept. The induced SnOx encapsulation layer on the surface of Pt NPs can protect Pt NPs from the poisoned of CO impurity in hydrogen oxidation reaction (HOR), and the HOR current density could still maintain 85% for 2000 s with 10,000 ppm CO in H2, while the commercial Pt/C is completely inactivated. In addition, the electrons transfer from SnOx to Pt NPs improved the HOR activity of the E-Pt-CNT@SnO2, achieving the excellent exchange current density of 1.55 A·mgPt—1. In situ Raman spectra and theoretical calculations show that the key to the electrochemical-method-induced SMSI is the formation of defects and the migration of SnOx caused by the electrochemical redox operation, and the weakening the Sn—O bond strength by Pt NPs.

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Journal of Electrochemistry

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Cite this article:
Li S-Z, Lin Z-J, Chen Q-A, et al. Electrochemical-Method-Induced Strong Metal-Support Interaction in Pt-CNT@SnO2 for CO-Tolerant Hydrogen Oxidation Reaction. Journal of Electrochemistry, 2024, 30(12). https://doi.org/10.61558/2993-074X.3474

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Received: 26 April 2024
Revised: 23 May 2024
Accepted: 02 June 2024
Published: 30 May 2024
© 2024 Xiamen University and Chinese Chemical Society.

This is an open access article under the CC BY 4.0 license (https://creativecommons.org/licenses/by/4.0/).