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• W4362602007 abstract "Enzymatic systems achieve the catalytic conversion of methane at room temperature under mild conditions. In this study, varying thermodynamic and kinetic parameters, we show that the reforming of methane by water (MWR, CH4 + H2O → CO + 3H2) and the water–gas shift reaction (WGS, CO + H2O → H2 + CO2), two essential processes to integrate fossil fuels toward a H2 energy loop, can be achieved on ZrO2/Cu(111) catalysts near room temperature. Measurements of ambient-pressure X-ray photoelectron spectroscopy and mass spectrometry, combined with density functional calculations and kinetic Monte Carlo simulations, were used to study the behavior of the inverse oxide/metal catalysts. The superior performance is associated with a unique zirconia–copper interface, where multifunctional sites involving zirconium, oxygen, and copper work coordinatively to dissociate methane and water at 300 K and move forward the MWR and WGS processes." @default.
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• W4362602007 date "2023-04-05" @default.
• W4362602007 modified "2023-10-18" @default.
• W4362602007 title "Activation and Conversion of Methane to Syngas over ZrO₂/Cu(111) Catalysts near Room Temperature" @default.
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• W4362602007 doi "https://doi.org/10.1021/jacs.3c01980" @default.
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• W4362602007 hasPublicationYear "2023" @default.
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