Unraveling the role of Fe5C2 in CH4 formation during CO2 hydrogenation over hydrophobic iron catalysts

被引:20
|
作者
Zhang, Zhenzhou [1 ]
Chen, Baojian [1 ]
Jia, Lingyu [1 ]
Liu, Wenqi [1 ]
Gao, Xinhua [2 ]
Gao, Jian [1 ]
Meng, Bo [1 ]
Tan, Yisheng [4 ]
He, Yurong [2 ,4 ]
Tu, Weifeng [1 ]
Han, Yi-Fan [1 ,3 ]
机构
[1] Zhengzhou Univ, Engn Res Ctr Adv Funct Mat Mfg, Sch Chem Engn, Minist Educ, Zhengzhou 450001, Peoples R China
[2] Ningxia Univ, Sch Chem & Chem Engn, State Key Lab High Efficiency Utilizat Coal & Gree, Yinchuan 750021, Peoples R China
[3] East China Univ Sci & Technol, State Key Lab Chem Engn, Shanghai 200237, Peoples R China
[4] Chinese Acad Sci, Inst Coal Chem, State Key Lab Coal Convers, Taiyuan 030001, Peoples R China
基金
中国国家自然科学基金;
关键词
Hydrophobic iron catalyst; H2O partial pressure; Pathways of CH4 formation; Product distribution regulation; Reaction mechanisms; FISCHER-TROPSCH SYNTHESIS; TOTAL-ENERGY CALCULATIONS; CARBON-DIOXIDE; LOWER OLEFINS; MN PROMOTER; CHI-FE5C2; FE; ACTIVATION; DFT; METHANATION;
D O I
10.1016/j.apcatb.2023.122449
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The production of value-added hydrocarbons by CO2 hydrogenation over iron (Fe) catalysts is an emerging platform reaction in CO2 utilization. However, CH4 forming in all hydrogenation reactions is undesirable. We focus on the role of Fe5C2 active species in CH4 formation during CO2 hydrogenation catalysis. Thus, Fe5C2 was manipulated by covering a hydrophobic shell to clarify the pathway of CH4 formation. By a combination of TPSR, in situ spectroscopies and DFT calculations, the variation in the mechanism of CH4 formation with the content of hydrophobic shell has been revealed. Meanwhile, the enhancement of H2O retention on the hydrophobic shell surface of Fe5C2 was found to inhibit the activation of CO2 by increasing energy barriers of C-C coupling re-actions. Deep insights into the tunable role of Fe5C2 in the formation of CH4 can help for the further design of high performance catalysts for this reaction.
引用
收藏
页数:12
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