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Engineering CNT-supported PtRu nanoparticles with an ultrathin carbon coating for an optimized d-band center and superior methanol oxidation performance.
PubMed
Authors: Wang X, Jiang Z, Deng B, Jiang ZJ
Year
2026
Paper ID
69128
Status
Peer-reviewed
Abstract Read
~2 min
Abstract Words
209
Citations
N/A
Abstract
Developing efficient and durable Pt-based catalysts for the methanol oxidation reaction (MOR) is crucial for direct methanol fuel cells (DMFCs), yet it remains a considerable challenge. This work demonstrates that using a carbon nanotube (CNT) support combined with an ultrathin carbon coating can enhance the activity and durability of PtRu alloyed nanoparticles (NPs) for the MOR. The developed CNT-supported PtRu NPs with an ultrathin carbon coating (CN@PtRu/CNTs) show significantly enhanced MOR activity and stability, primarily arising from their unique structural features, including the CNT support, ultrathin carbon coating, and Ru alloying. The CNT support provides a high surface area and excellent conductivity, aiding efficient electron transfer. The ultrathin carbon coating stabilizes the PtRu NPs by preventing agglomeration and detachment and enhances electronic interactions, boosting catalytic performance. The Ru alloying modifies the electronic structure of Pt, improving catalytic properties and resistance to CO poisoning. The CN@PtRu/CNTs exhibit a significantly higher MOR mass activity and stability than commercial Pt/C. They also show great potential for practical DMFC applications, achieving higher power density and durability than Pt/C. DFT calculations indicate that the CNT support and CN coating improve the d-band center of Pt, facilitating key MOR steps, while Ru alloying enhances *OH adsorption, accelerating *CO oxidation.
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- This paper contributes to the Quantum Chemistry research area in the Quantum Articles archive.
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- Developing efficient and durable Pt-based catalysts for the methanol oxidation reaction (MOR) is crucial for direct methanol fuel cells (DMFCs), yet it remains a considerable...
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