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Research Article

Structure engineering of PtCu3/C catalyst from disordered to ordered intermetallic compound with heat-treatment for the methanol electrooxidation reaction

Zihao Xing1Jun Li1Shun Wang1Chenliang Su2( )Huile Jin1( )
Institute of New Materials & Industry Technology, Wenzhou University, Wenzhou 325024, China
Institute of Microscale Optoelectronics, Shenzhen University, Shenzhen 518060, China
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Graphical Abstract

The intermetallic compound of PtCu3/C-1000 exhibited high specific activity of 3.23 mA·cm–1 and mass activity of 1,200 mA·mgPt–1 towards the methanol electrooxidation reaction.

Abstract

Platinum based alloys are hereinto the mostly used methanol oxidation catalysts. However, there are limited ways to improve the methanol oxidation reaction (MOR) performance of catalysts in terms of both activity and stability. Herein we developed a simple heat-treatment method to synthesize PtCu3/C intermetallic compound catalyst with lattice compression. The as-prepared PtCu3/C-1000 exhibited high specific activity of 3.23 mA·cm–1 and mass activity of 1,200 mA·mgPt–1, which is much higher than the PtCu3/C-untreated and commercial Pt/C catalysts, respectively. The XAS and DFT results shows the high activity of the catalyst towards MOR comes from the tightening of the Pt-M bond, which leads to the decrease of Fermi energy level and the make it difficulty in adsorbing carbon intermediates, thus releasing more active sites to promote the improvement of MOR performance. Moreover, the PtCu3/C-1000 shows better stability which is due to the surface-rich Pt prevents Cu from dissolution.

Electronic Supplementary Material

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Nano Research
Pages 3866-3871
Cite this article:
Xing Z, Li J, Wang S, et al. Structure engineering of PtCu3/C catalyst from disordered to ordered intermetallic compound with heat-treatment for the methanol electrooxidation reaction. Nano Research, 2022, 15(5): 3866-3871. https://doi.org/10.1007/s12274-021-3993-8
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Received: 15 October 2021
Revised: 08 November 2021
Accepted: 10 November 2021
Published: 17 December 2021
© Tsinghua University Press and Springer-Verlag GmbH Germany, part of Springer Nature 2021
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