Exploring the Effects of the Interaction of Carbon and MoS2 Catalyst on CO2 Hydrogenation to Methanol |
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Authors: | Pingping Cui Ruyu Sun Linfei Xiao Wei Wu |
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Affiliation: | National Center for International Research on Catalytic Technology, Key Laboratory of Chemical Engineering Process & Technology for High-Efficiency Conversion, College of Heilongjiang Province, School of Chemistry and Material Sciences, Heilongjiang University, Harbin 150080, China; (P.C.); (R.S.) |
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Abstract: | Hydrogenation of CO2 to form methanol utilizing green hydrogen is a promising route to realizing carbon neutrality. However, the development of catalyst with high activity and selectivity to methanol from the CO2 hydrogenation is still a challenge due to the chemical inertness of CO2 and its characteristics of multi-path conversion. Herein, a series of highly active carbon-confining molybdenum sulfide (MoS2@C) catalysts were prepared by the in-situ pyrolysis method. In comparison with the bulk MoS2 and MoS2/C, the stronger interaction between MoS2 and the carbon layer was clearly generated. Under the optimized reaction conditions, MoS2@C showed better catalytic performance and long-term stability. The MoS2@C catalyst could sustain around 32.4% conversion of CO2 with 94.8% selectivity of MeOH for at least 150 h. |
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Keywords: | MoS2@C carbon dioxide hydrogenation methanol |
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