AuAg@Pt Nanowires with Controlled Electronic and Morphological Characteristics for Oxygen Reduction Electrocatalysis

Developing highly active and durable electrocatalysts for oxygen reduction reaction (ORR) is critical for the widespread use of next‐generation power sources, such as proton exchange membrane fuel cells. Herein, we report the synthesis of 1D AuAg@Pt core–shell nanowires (AuAg@Pt NWs) as an advanced ORR catalyst. A unique feature of this catalyst is a significant counterintuitive compressive strain applied to its Pt shell, which can be attributed to the high density of grain boundaries in the AuAg NW core. This strain can induce a downward shift of the Pt d‐band center, leading to an optimized binding energy for oxygen species. Consequently, the prepared AuAg@Pt NWs exhibited enhanced ORR activity compared to core–shell nanorods with a low density of grain boundaries and a commercial Pt/C catalyst. Furthermore, they showed outstanding durability for repeated ORR operation due to their 1D wire structure that can effectively protect them against particle agglomeration. This work highlights a rational design strategy that combines electronic and morphological engineering to devise advanced, stable electrocatalysts.

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Publication Details

Journal
ChemNanoMat
Published
2025-11-22
DOI
https://doi.org/10.1002/cnma.202500491
Primary Topic
Electrocatalysts for Energy Conversion
Type
article
Field-Weighted Citation Impact
0.00

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article

AuAg@Pt Nanowires with Controlled Electronic and Morphological Characteristics for Oxygen Reduction Electrocatalysis

Sang Woo Han, Heon Chul Kim, Jong Wook Hong, Bon Seung Goo et al.
ChemNanoMat
Electrocatalysts for Energy Conversion
article

AuAg@Pt Nanowires with Controlled Electronic and Morphological Characteristics for Oxygen Reduction Electrocatalysis

Sang Woo Han, Heon Chul Kim, Jong Wook Hong, Bon Seung Goo, Yongmin Kwon, Eun‐Jin Lee
article en

Abstract

Developing highly active and durable electrocatalysts for oxygen reduction reaction (ORR) is critical for the widespread use of next‐generation power sources, such as proton exchange membrane fuel cells. Herein, we report the synthesis of 1D AuAg@Pt core–shell nanowires (AuAg@Pt NWs) as an advanced ORR catalyst. A unique feature of this catalyst is a significant counterintuitive compressive strain applied to its Pt shell, which can be attributed to the high density of grain boundaries in the AuAg NW core. This strain can induce a downward shift of the Pt d‐band center, leading to an optimized binding energy for oxygen species. Consequently, the prepared AuAg@Pt NWs exhibited enhanced ORR activity compared to core–shell nanorods with a low density of grain boundaries and a commercial Pt/C catalyst. Furthermore, they showed outstanding durability for repeated ORR operation due to their 1D wire structure that can effectively protect them against particle agglomeration. This work highlights a rational design strategy that combines electronic and morphological engineering to devise advanced, stable electrocatalysts.

ChemNanoMatVol. 12(1)
Korea Advanced Institute of Science and Technology (KR), Fuel Cells and Hydrogen (BE), Korea Energy Economics Institute (KR), Korea Institute of Energy Research (KR)
National Research Foundation, National Research Foundation of Korea, Ministry of Science and ICT, South Korea
Openalex Percentile: Top 75%
Electrocatalysts for Energy Conversion
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AuAg@Pt Nanowires with Controlled Electronic and Morphological Characteristics for Oxygen Reduction Electrocatalysis — Sang Woo Han, Heon Chul Kim, et al. · ChemNanoMat (2025) | TGRS Research Map | TGRS