4.6 Article

Transition of surface phase of cobalt oxide during CO oxidation

Journal

PHYSICAL CHEMISTRY CHEMICAL PHYSICS
Volume 20, Issue 9, Pages 6440-6449

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c7cp07407g

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Funding

  1. Chemical Sciences, Geosciences and Biosciences Division, Office of Basic Energy Sciences, Office of Science, U.S. Department of Energy [DE-SC0014561]

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In situ/operando studies of a heterogeneous catalyst are particularly valuable for achieving a fundamental understanding of catalytic mechanisms at a molecular level by establishing a correlation between the observed catalytic performance and the corresponding surface chemistry during catalysis. Herein, CO oxidation on cobalt oxides was studied via ambient pressure X-ray photoelectron spectroscopy (AP-XPS). During CO oxidation on CoO in the temperature range of 140-180 degrees C, the active surface phase of CoO progressively transforms to Co3O4. Kinetic studies of CO oxidation on the surface phase CoO at 80-120 degrees C and on the formed Co3O4 at 160-220 degrees C show that CoO and Co3O4 exhibit different activation barriers: 49.3 kJ mol(-1) for CoO and 36.9 kJ mol(-1) for Co3O4. This study demonstrates the transition of the active surface phase of a transition metal oxide-based catalyst under catalytic conditions with no change in the bulk phase of the catalyst.

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