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Abstract:
A new adsorbate-mediated strategy was developed to enhance the metal-support interaction of Cu/CeO 2 , aiming to improve its catalytic activity and sintering resistance in the water-gas shift (WGS) reaction. By treating Cu/CeO 2 in a 20CO 2 /2H 2 gas mixture for the formation of surface HCO n (n = 2, 3), there was significant enhancement of the interaction between CeO 2 and Cu. The HCO n adsorbate was removed through calcination in an O 2 /Ar atmosphere at 400 °C for 6 h. The as-obtained Cu/CeO 2 catalyst was compared with the untreated counterpart in the WGS reaction. It was observed that CO conversion at 350 °C was 86% and 47%, respectively, over the two catalysts. The superiority of the former is attributed to the enhanced interaction between Cu and CeO 2 . In a run of 15 h at 400 °C, the treated catalyst showed no obvious sign of deactivation. © 2018 American Chemical Society.
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ACS Applied Energy Materials
ISSN: 2574-0962
Year: 2018
Issue: 4
Volume: 1
Page: 1408-1414
5 . 5 0 0
JCR@2023
ESI HC Threshold:284
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ESI Highly Cited Papers on the List: 0 Unfold All
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30 Days PV: 2
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