Mechanochemical synthesis of Ni-Co bimetallic catalyst for enhanced hydrogenation of carbon dioxide to methane

被引:0
|
作者
Chen, Haipeng [1 ]
Hao, Peinan [1 ]
Liu, Jiameng [1 ]
Zhou, Guangqing [1 ]
Lv, Xinshuai [1 ]
Zhang, Ruoyu [1 ]
Wei, Yiting [1 ]
Li, Wenqiang [1 ]
Zhou, Shixue [2 ]
Feng, Xun [1 ]
机构
[1] Luoyang Normal Univ, Coll Chem & Chem Engn, Henan Key Lab Funct Oriented Porous Mat, Luoyang 471934, Peoples R China
[2] Shandong Univ Sci & Technol, Coll Chem & Biol Engn, Qingdao 266590, Peoples R China
基金
中国国家自然科学基金;
关键词
Carbon dioxide; Methane; Bimetallic catalyst; Mechanochemical synthesis; H; 2; activation; IN-SITU; EFFICIENT HYDROGENATION; COBALT; NICKEL; NANOPARTICLES; MECHANISM; XPS;
D O I
10.1016/j.apsusc.2025.162756
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
Using renewable hydrogen and inexpensive catalysts, the catalytic hydrogenation of CO2 to CH4 is a promising strategy for storing renewable energy. Herein, a Ni-Co bimetallic catalyst was developed with a mechanochemical synthesis method for highly active and selective CO2 methanation. Under conditions of 360 degrees C, 0.1 MPa and 9600 mL h- 1 gcat -1 , the selectivity to CH4 achieves 99.8 % at a CO2 conversion of 84.5 % and a CH4 space-time yield (STY) of 1325.6 g kg-1 h- 1, outperforming the previous reports under similar reaction conditions. The transfer of electrons from Ni to Co can result in the formation of electron-rich Co species, which not only enhances CO2 adsorption but also facilitates H2 dissociation through the electron donation and back-donation mechanism. Experimental and theoretical investigations demonstrate that CO2 methanation commences with CO2 dissociation into CO* and O* species, subsequently proceeding with carbon terminal hydrogenation, followed by the execution of three exothermic reactions via CH*, CH2*, and CH3* species. This work contributes to the design and synthesis of cheap and efficient catalysts for hydrogenation of CO2 to CH4.
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页数:9
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