首页|Zonal activation of molecular carbon dioxide and hydrogen over dual sites Ni-Co-MgO catalyst for CO2 methanation:Synergistic catalysis of Ni and Co species

Zonal activation of molecular carbon dioxide and hydrogen over dual sites Ni-Co-MgO catalyst for CO2 methanation:Synergistic catalysis of Ni and Co species

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An in-depth mechanism in zonal activation of CO2 and H2 molecular over dual-active sites has not been revealed yet.Here,Ni-Co-MgO was rationally constructed to elucidate the CO2 methanation mechanism.The abundant surface nickel and cobalt components as active sites led to strong Ni-Co interaction with charge transfer from nickel to cobalt.Notably,electron-enriched Coδ-species participated in efficient chemisorption and activation of CO2 to generate monodentate carbonate.Simultaneously,plentiful avail-able Ni0 sites facilitated H2 dissociation,thus CO2 and H2 were smoothly activated at zones of Coδ-species and Ni0,respectively.Detailed in situ DRIFTS,quasi situ XPS,TPSR,and DFT calculations substantiated a new formate evolution mechanism via monodentate carbonate instead of traditional bidentate carbonate based on synergistic catalysis of Coδ-species and Ni0.The zonal activation of CO2 and H2 by tuning elec-tron behaviors of double-center catalysts can boost heterogeneous catalytic hydrogenation performance.

Zonal activationCO2 methanationDual active sitesSynergistic effect

Zonglin Li、Jianjun Chen、Yu Xie、Junjie Wen、Huiling Weng、Mingxue Wang、Jingyi Zhang、Jinyan Cao、Guocai Tian、Qiulin Zhang、Ping Ning

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Faculty of Environmental Science and Engineering,Kunming University of Science and Technology,Kunming 650500,Yunnan,China

National-Regional Engineering Center for Recovery of Waste Gases from Metallurgical and Chemical Industries,Kunming University of Science and Technology,Kunming 650500,Yunnan,China

Faculty of Metallurgical and Energy Engineering,Kunming University of Science and Technology,Kunming 650093,Yunnan,China

Science and Technology Project of Southwest United Graduate School of Yunnan Province国家自然科学基金

202302AQ37000222206066

2024

能源化学
中国科学院大连化学物理研究所 中国科学院成都有机化学研究所

能源化学

CSTPCDEI
影响因子:0.654
ISSN:2095-4956
年,卷(期):2024.91(4)
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