Pd-Ru pair on Pt surface for promoting hydrogen oxidation and evolution in alkaline media

Hydrogen oxidation reaction in alkaline media is critical for alkaline fuel cells and electrochemical ammonia compressors. The slow hydrogen oxidation reaction in alkaline electrolytes requires large amounts of scarce and expensive platinum catalysts. While transition metal decoration can enhance Pt catalysts' activity, it often reduces the electrochemical active surface area, limiting the improvement in Pt mass activity. Here, we enhance Pt catalysts' activity without losing surface-active sites by using a Pd-Ru pair. Utilizing a mildly catalytic thermal pyrolysis approach, Pd-Ru pairs are decorated on Pt, confirmed by extended X-ray absorption fine structure and high-angle annular dark-field scanning transmission electron microscopy. Density functional theory and ab-initio molecular dynamics simulations indicate preferred Pd and Ru dopant adsorption. The Pd-Ru decorated Pt catalyst exhibits a mass-based exchange current density of 1557 ± 85 A g<sup>-1</sup><sub>metal</sub> for hydrogen oxidation reaction, demonstrating superior performance in an ammonia compressor.

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Publication Details

Journal
Nature Communications
Published
2024-08-23
DOI
https://doi.org/10.1038/s41467-024-51480-w
Citations
23
Primary Topic
Electrocatalysts for Energy Conversion
Type
article
Field-Weighted Citation Impact
2.35

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article

Pd-Ru pair on Pt surface for promoting hydrogen oxidation and evolution in alkaline media

Enyuan Hu, Kai He, Perla B. Balbuena, Longsheng Cao et al.
23 citations
Nature Communications
Electrocatalysts for Energy Conversion
2.35
article

Pd-Ru pair on Pt surface for promoting hydrogen oxidation and evolution in alkaline media

Enyuan Hu, Kai He, Perla B. Balbuena, Longsheng Cao, Xiner Lu, David A. Cullen, Nico Eidson, Xiao‐Qing Yang, Chunsheng Wang, Dan Li, Tao Deng, Fernando A. Soto
article en
23 citations

Abstract

Hydrogen oxidation reaction in alkaline media is critical for alkaline fuel cells and electrochemical ammonia compressors. The slow hydrogen oxidation reaction in alkaline electrolytes requires large amounts of scarce and expensive platinum catalysts. While transition metal decoration can enhance Pt catalysts' activity, it often reduces the electrochemical active surface area, limiting the improvement in Pt mass activity. Here, we enhance Pt catalysts' activity without losing surface-active sites by using a Pd-Ru pair. Utilizing a mildly catalytic thermal pyrolysis approach, Pd-Ru pairs are decorated on Pt, confirmed by extended X-ray absorption fine structure and high-angle annular dark-field scanning transmission electron microscopy. Density functional theory and ab-initio molecular dynamics simulations indicate preferred Pd and Ru dopant adsorption. The Pd-Ru decorated Pt catalyst exhibits a mass-based exchange current density of 1557 ± 85 A g<sup>-1</sup><sub>metal</sub> for hydrogen oxidation reaction, demonstrating superior performance in an ammonia compressor.

Nature CommunicationsVol. 15(1)
Oak Ridge National Laboratory (US), Pennsylvania State University (US), Brookhaven National Laboratory (US), University of California, Irvine (US), Irvine University (US), UPMC McKeesport (US), University of Maryland, College Park (US), Texas A&M University (US)
U.S. Department of Energy, University of Texas at Austin, Office of Science, American Chemical Society Petroleum Research Fund, Oak Ridge National Laboratory, Brookhaven National Laboratory
Openalex Percentile: Top 11%
Electrocatalysts for Energy Conversion
2.35
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