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Cited 6 time in webofscience Cited 10 time in scopus
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Alleviating inhibitory effect of H2 on low-temperature water-gas shift reaction activity of Pt/CeO2 catalyst by forming CeO2 nano-patches on Pt nano-particles

Authors
Lee, J.[Lee, J.]Shin, D.[Shin, D.]Lee, E.[Lee, E.]Li, C.[Li, C.]Kim, J.M.[Kim, J.M.]Han, J.W.[Han, J.W.]Kim, D.H.[Kim, D.H.]
Issue Date
15-May-2022
Publisher
Elsevier B.V.
Keywords
CeO2 nano-patch; Excess H2; In-situ diffuse reflectance infrared Fourier transform spectroscopy; Low temperature water-gas shift reaction; Pt nano-particle
Citation
Applied Catalysis B: Environmental, v.305
Indexed
SCIE
SCOPUS
Journal Title
Applied Catalysis B: Environmental
Volume
305
URI
https://scholarworks.bwise.kr/skku/handle/2021.sw.skku/94715
DOI
10.1016/j.apcatb.2021.121038
ISSN
0926-3373
Abstract
Pt/CeO2 has gained much attention for their high activity in low-temperature (LT) water-gas shift (WGS) reaction. However, the inclusion of H2 in the feed as in the practical reaction condition significantly degrades the LT-WGS activity of the Pt/CeO2 catalysts. In this contribution, the activity of Pt/CeO2 catalyst under the feed gas containing excess H2 (20 vol% of H2) was enhanced more than three times by forming CeO2 nano-patches on Pt nano-particles. Both in-situ diffuse reflectance infrared Fourier transform spectroscopy and density functional theory calculation results indicate that dissociated H2 on the Pt nano-particle inhibits the activity of the Pt/CeO2 catalysts by occupying the active sites (Pt nano-particle-CeO2 interface). On the other hand, thin CeO2 nano-patches on Pt nano-particle suppressed the H2 dissociation. As a result, the WGS reactivity of the active Pt nano-particle-CeO2 interface was less affected by H2, granting the catalysts the high activity under the practical reaction conditions. © 2021 Elsevier B.V.
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