Regulating the Cu+ distribution by the controllable metal-support interaction via thermal treatment for boosting reverse water–gas shift reaction
- Authors
- Liu, Qiufeng; Sun, Kaihang; Lu, Kun; Xie, Xingwei; Zhang, Longzhou; Kim, Young Dok; Liu, Zhongyi; Peng, Zhikun
- Issue Date
- 15-Jun-2025
- Publisher
- Academic Press Inc.
- Keywords
- CO<sub>2</sub> hydrogenation; Cu<sup>+</sup> ratio; Metal-support interaction; Y<sub>2</sub>O<sub>3</sub>
- Citation
- Journal of Colloid and Interface Science, v.688, pp 517 - 525
- Pages
- 9
- Indexed
- SCIE
SCOPUS
- Journal Title
- Journal of Colloid and Interface Science
- Volume
- 688
- Start Page
- 517
- End Page
- 525
- URI
- https://scholarx.skku.edu/handle/2021.sw.skku/121105
- DOI
- 10.1016/j.jcis.2025.02.154
- ISSN
- 0021-9797
1095-7103
- Abstract
- Metal-support interaction (MSI) is an efficient strategy to modulate the distribution of active metal with different electronic states over the oxide-supported metal catalysts. However, the intrinsic correlation between the intensity of MSI and the electronic structure of supported metals remains inadequate. In this work, the intensity of MSI over the Cu/Y2O3 catalyst was tuned by the calcination temperature, which regulated the distribution of Cu0, Cu+ and Cu2+ species. The Cu/Y2O3 catalyst with the highest amount of Cu+ exhibits the superior performance of reverse water–gas shift reaction. Due to the enhanced H2 activation and promoted charge transfer at the interfacial Cu+/Y2O3 site based on the experimental characterizations, the CO formation rate reached 220 mmolCOgcat−1 h−1 at 500 °C. The present work provides an efficient way to regulate the supported metal species with the specific electronic state. © 2025 Elsevier Inc.
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Collections - Graduate School > Chemistry > 1. Journal Articles

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