Abstract
In the field of noble metal-catalyzed alcohol electro-oxidation reaction (AOR), huge attention is paid on the composition, size, facet, and structure of the metals, while the support engineering should also be emphasized. CeO2 has been widely used as an unique support in AOR, primarily due to its abundant oxygen vacancies (Ov). Herein, we report CeO2·xH2O nanoparticles with both massive hydroxyl groups (OH) and Ov remarkably enhance the catalytic activity and stability of Pd toward ethanol oxidation reaction (EOR). The CO striping experiments and density functional theory (DFT) calculations suggest that OH and Ov on CeO2·xH2O surface bring about a large downshift of Pd d-band center and a significant weakening of CO absorption on Pd. Moreover, OH and Ov also play synergic roles in the removal of toxic intermediates. Consequently, the important roles of OH and Ov of CeO2·xH2O are confirmed in Pd-catalyzed EOR. The facile CeO2·xH2O-enhanced strategy can contribute to the catalyst design for other energy conversion reactions.
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Acknowledgements
This work was supported by the National Natural Science Foundation of China (21875125, 22161033), the 111 Project (D20033), the Natural Science Foundation of Inner Mongolia Autonomous Region of China (2017JQ03), “Grassland Talent” Program and “Grassland Talent” Innovation Team of Inner Mongolia.
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Li, Z., Li, J., Zheng, Z. et al. Roles of hydroxyl and oxygen vacancy of CeO2·xH2O in Pd-catalyzed ethanol electro-oxidation. Sci. China Chem. 65, 877–884 (2022). https://doi.org/10.1007/s11426-021-1220-2
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DOI: https://doi.org/10.1007/s11426-021-1220-2