Exploring the Effects of the Interaction of Carbon and MoS2 Catalyst on CO2 Hydrogenation to Methanol

被引:10
|
作者
Cui, Pingping [1 ]
Sun, Ruyu [1 ]
Xiao, Linfei [1 ]
Wu, Wei [1 ]
机构
[1] Heilongjiang Univ, Key Lab Chem Engn Proc & Technol High Efficiency, Coll Heilongjiang Prov, Natl Ctr Int Res Catalyt Technol,Sch Chem & Mat S, Harbin 150080, Peoples R China
关键词
MoS2@C; carbon dioxide; hydrogenation; methanol; HETEROJUNCTION NANOSTRUCTURE; OXYGEN EVOLUTION; METHANATION; PERFORMANCE; CU/SIO2; VACANCY; OXIDE; INTERMEDIATE; INSIGHT;
D O I
10.3390/ijms23095220
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页数:15
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