4.8 Article

In situ atomic-scale imaging of the metal/oxide interfacial transformation

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NATURE COMMUNICATIONS
卷 8, 期 -, 页码 -

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NATURE PUBLISHING GROUP
DOI: 10.1038/s41467-017-00371-4

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  1. U.S. Department of Energy, Office of Basic Energy Sciences, Division of Materials Sciences and Engineering [DE-SC0001135]
  2. National Science Foundation [CBET-1264940, CMMI-105661]
  3. U.S. Department of Energy, Office of Basic Energy Sciences [DE-SC0012704]
  4. National Science Foundation grant [OCI-1053575]
  5. Directorate For Engineering
  6. Div Of Chem, Bioeng, Env, & Transp Sys [1264940] Funding Source: National Science Foundation

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Directly probing structure dynamics at metal/oxide interfaces has been a major challenge due to their buried nature. Using environmental transmission electron microscopy, here we report observations of the in-place formation of Cu2O/Cu interfaces via the oxidation of Cu, and subsequently probe the atomic mechanisms by which interfacial transformation and grain rotation occur at the interfaces during reduction in an H-2 gas environment. The Cu2O. Cu transformation is observed to occur initially along the Cu2O/Cu interface in a layer-by-layer manner. The accumulation of oxygen vacancies at the Cu2O/Cu interface drives the collapse of the Cu2O lattice near the interface region, which results in a tilted Cu2O/Cu interface with concomitant Cu2O island rotation. These results provide unprecedented microscopic detail regarding the redox reactions of supported oxides, which differs fundamentally from the reduction of bulk or isolated oxides that requires the formation of new interfaces between the parent oxide and the reduced phase.

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