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Flame-Made Surface-Substituted Copper-Ceria as an Excellent Reverse Water-Gas Shift Reaction Catalyst via Three
Bingqiao Xie1,2, Yi Fen Zhu2, Mahdi Shakeri1
1Institute of Chemical Sciences and Engineering (ISIC), École Polytechnique Fédérale de Lausanne (EPFL), Lausanne 1015, Switzerland.
Abstract:
The limited mechanistic understanding and ambiguous structure-performance relationships have hindered the optimization of Cu-based catalysts for the reverse water-gas shift (rWGS) reaction. Here, we report a flame spray pyrolysis (FSP)-derived Cu-CeO2 catalyst featuring highly dispersed, surface-substituted Cu+ species (CuyCe1-yO2-x) anchored on a defect-rich ceria matrix. This catalyst demonstrates excellent stability and outstanding rWGS activity at 600 °C, achieving a CO production rate of 8094 mmol/gcat./h, surpassing the conventional Cu-CeO2 catalyst and other reported rWGS catalysts. In situ spectroscopic analyses, supported by DFT calculations, reveal three parallel reaction pathways in which carboxylate- and formate-mediated routes proceed at distinct active sites. A clear structure-activity correlation is established across Cu+, Cu0, and ceria defect sites in the FSP-derived catalysts. Notably, a previously underexplored carboxylate-mediated pathway, facilitated on the surface-substituted Cu+ structure, is identified as the dominant route, featuring a significantly lower apparent activation energy (20-30 kJ/mol) compared to the classical formate pathway.
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