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Atomic-thick metastable phase RhMo nanosheets for hydrogen oxidation catalysis

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Hu,  Zhiwei
Zhiwei Hu, Physics of Correlated Matter, Max Planck Institute for Chemical Physics of Solids, Max Planck Society;

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Citation

Zhang, J., Liu, X., Ji, Y., Liu, X., Su, D., Zhuang, Z., et al. (2023). Atomic-thick metastable phase RhMo nanosheets for hydrogen oxidation catalysis. Nature Communications, 14(1): 1761, pp. 1-9. doi:10.1038/s41467-023-37406-y.


Cite as: https://hdl.handle.net/21.11116/0000-000D-015A-D
Abstract
Metastable phase two-dimensional catalysts provide great flexibility for modifying their chemical, physical, and electronic properties. However, the synthesis of ultrathin metastable phase two-dimensional metallic nanomaterials is highly challenging, mainly due to the anisotropic nature of metallic materials and their thermodynamically unstable ground-state. Here, we report free-standing RhMo nanosheets with atomic thickness and a unique core/shell (metastable phase/stable phase) structure. The polymorphic interface between the core region and shell region stabilizes and activates metastable phase catalysts; the RhMo Nanosheets/C shows excellent hydrogen oxidation activity and stability. Specifically, the mass activities of RhMo Nanosheets/C is 6.96 A mgRh−1; this is 21.09 times higher than that of commercial Pt/C (0.33 A mgPt−1). Density functional theory calculations suggest that the interface aids in the dissociation of H2 and the H species can then spillover to weak H binding sites for desorption, providing excellent hydrogen oxidation activity for RhMo nanosheets. This work advances the highly controlled synthesis of two-dimensional metastable phase noble metals and provides great directions for the design of high-performance catalysts for fuel cells and beyond. © 2023, The Author(s).