Ultrathin urchin-like PdPtCu alloys anchored CeO2 nanosheets for efficient methanol oxidation
- Authors
- Kim, Hyeon Jeong; Park, Dae Keun; Theerthagiri, Jayaraman; Hong, Jong Wook; Choi, Myong Yong; Lee, Young Wook
- Issue Date
- Apr-2026
- Publisher
- Chinese Society of Metals
- Keywords
- Metal oxide supports; PdPtCu alloy on CeO2 nanosheets; Electrocatalysis; Methanol oxidation reaction; ligand-exchange method
- Citation
- Journal of Materials Science & Technology, v.250, pp 197 - 204
- Pages
- 8
- Indexed
- SCOPUS
- Journal Title
- Journal of Materials Science & Technology
- Volume
- 250
- Start Page
- 197
- End Page
- 204
- URI
- https://scholarworks.gnu.ac.kr/handle/sw.gnu/80040
- DOI
- 10.1016/j.jmst.2025.07.002
- ISSN
- 1005-0302
1941-1162
- Abstract
- Platinum-based catalysts, particularly Pt/C, are widely employed in direct methanol fuel cells (DMFCs); however, their practical deployment is hindered by severe drawbacks, including carbon support corrosion and the high cost of Pt, which collectively compromise long-term durability and economic feasibility. To overcome these limitations, we present the design of an ultrathin, urchin-like PdPtCu ternary alloy supported on CeO2 nanosheets, specifically engineered to enhance both the activity and stability of the methanol oxidation reaction (MOR). A central innovation of this work lies in the employment of a CuO-CeO2 composite support, which enables efficient incorporation of copper via an acid-mediated ligand exchange process-addressing the inherent challenge of immobilizing metallic species on oxide surfaces. The incorporation of CuO facilitates the oxidative activation of copper species, while CeO2 contributes structural robustness and redox-active sites that promote intermediate removal during MOR. The resulting PdPtCu-CeO2 nanostructures exhibit a high surface area and unique urchin-like morphology, both of which contribute to markedly enhanced electrochemical performance. Compared to commercial Pt/C, the PdPtCu-CeO2 catalyst demonstrates approximately threefold enhancements in both mass and specific activities, along with excellent long-term durability as confirmed by chronoamperometric measurements. This work study highlights the promise of oxide-derived hybrid supports and multi-metallic nanostructures for advancing cost-effective and durable electrocatalysts for DMFC applications, thereby advancing the pursuit of next-generation, carbon-free catalyst platforms. (c) 2025 Published by Elsevier Ltd on behalf of The editorial office of Journal of Materials Science & Technology.
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