Home > Publications database > Self-Epitaxial Hetero-Nanolayers and Surface Atom Reconstruction in Electrocatalytic Nickel Phosphides |
Journal Article | FZJ-2020-02731 |
; ; ;
2020
Soc.
Washington, DC
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Please use a persistent id in citations: http://hdl.handle.net/2128/25896 doi:10.1021/acsami.0c03154
Abstract: Surface atomic, compositional, and electronic structures play decisive roles in governing the performance of catalysts during electrochemical reactions. Nevertheless, for efficient and cheap transition-metal phosphides used for water splitting, such atomic-scale structural information is largely missing. Despite much effort being made so far, there is still a long way to go for establishing a precise structure–activity relationship. Here, in combination with electron-beam bombardment and compositional analysis, our atomic-scale transmission electron microscopy study on Ni5P4 nanosheets, with a preferential (001) orientation, directly reveals the coverage of a self-epitaxial Ni2P nanolayer on the phosphide surface. Apart from the presence of nickel vacancies in the Ni5P4 phase, our quantum-mechanical image simulations also suggest the existence of an additional NiPx (0 < x < 0.5) nanolayer, characteristic of complex surface atom reconstruction, on the outermost surface of the phosphides. The surface chemical gradient and the core–shell scenario, probably responsible for the passivated catalytic activity, provide a novel insight to understand the catalytic performance of transition-metal catalysts used for electrochemical energy conversion.
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