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Research Article | Open Access

Cu-doped CeMnO2-supported Pt catalysts with high activity at industrial operating conditions for preferential CO oxidation in H2

Jianlin Cao1,#Tao Xing2,#Zongzhuang Sun1Sheng Wei1Jiaqi Wang1Lexin Mao1Tao Liu2Zhi Li2Yongxiao Tuo1Xin Zhou4 ( )Hao Yan1Yibin Liu1Xiang Feng1 ( )Chaohe Yang1De Chen3 ( )
State Key Laboratory of Heavy Oil Processing, China University of Petroleum (East China), Qingdao 266000, China
Shandong Energy Group Co., Ltd., Jinan 250000, China
Department of Chemical Engineering, Norwegian University of Science and Technology, Trondheim 7491, Norway
Department of Chemistry and Chemical Engineering, Ocean University of China, Qingdao 266100, China

#Jianlin Cao and Tao Xing contributed equally to this work.

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Abstract

Developing efficient, stable, and inexpensive catalysts for the preferential CO oxidation in H2 (CO-PROX) over a wide temperature range in the presence of CO2 and H2O is indispensable for the hydrogen purification process. Herein, CuO was introduced to the CeMnO2-supported Pt catalyst to modulate the oxygen activation capacity and provide the available number of active sites in CO-PROX. One part of the CuO species doped into CeO2 strongly interacts with Ce, thus enhancing the oxygen transfer capacity of the catalyst. The other part of CuO species located on the surface of the catalyst provides extra Cu+ sites available for low-temperature CO adsorption. This synergistic interaction with Pt sites further enhances CO and O2 activation, broadening the temperature window of high activity. The optimal Pt-10CuO/CeMnO2 catalyst exhibits complete CO conversion (CO/O2 ratio of 1:1) within the practical temperature range of 130–190 °C, even in the presence of CO2 and H2O, and remains stable at 150 °C for 76 h testing without any deactivation. This work will give a novel approach for the design of highly efficient inexpensive catalysts for industrial preferential oxidation of CO in H2, especially in the presence of CO2 and H2O.

Graphical Abstract

The CuO doped into the lattice of CeO2 enhanced the oxygen transfer capacity and the CuO species on the surface of catalyst provided Cu+ sites. The coupling of these two functions by CuO ensured the selective and efficient conversion of CO.

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Carbon Future
Article number: 9200038

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Cite this article:
Cao J, Xing T, Sun Z, et al. Cu-doped CeMnO2-supported Pt catalysts with high activity at industrial operating conditions for preferential CO oxidation in H2. Carbon Future, 2025, 2(2): 9200038. https://doi.org/10.26599/CF.2025.9200038
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Received: 25 November 2024
Revised: 25 January 2025
Accepted: 04 February 2025
Published: 14 March 2025
© The author(s) 2025. Published by Tsinghua University Press.

Open AccessThis article is licensed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits use, sharing, distribution and reproduction in any medium, provided the original work is properly cited.