Ni nanoparticles dispersed on oxygen vacancies-rich CeO2 nanoplates for enhanced low-temperature CO2 methanation performance

被引:78
|
作者
Du, Yixiong [1 ]
Qin, Chuan [1 ]
Xu, Yanfei [1 ]
Xu, Di [2 ]
Bai, Jingyang [1 ]
Ma, Guangyuan [1 ]
Ding, Mingyue [1 ,3 ]
机构
[1] Wuhan Univ, Sch Power & Mech Engn, Inst Technol Sci, Hubei Prov Key Lab Accoutrement Tech Fluid Machin, Wuhan 430072, Peoples R China
[2] Wuhan Univ, Coll Chem & Mol Sci, Wuhan 430072, Peoples R China
[3] Wuhan Univ, Shenzhen Res Inst, Shenzhen 518108, Peoples R China
基金
中国国家自然科学基金;
关键词
Low-temperature CO2 methanation; Oxygen vacancies; Ceria; NiO-CeO2; structure; CATALYSTS; SURFACE; CERIA; HYDROGEN; SUPPORT; PROMOTION; REMOVAL; NI/CEO2;
D O I
10.1016/j.cej.2021.129402
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Developing efficient catalysts with superior low-temperature catalytic performance is highly promising yet challenging for CO2 methanation. Here we synthesized a nanoplate-shaped CeO2, which was rich in oxygen vacancies, as the carrier to disperse the nickel nanoparticles. The resultant catalyst (Ni/CeO2-P) showed remarkable low-temperature CO2 methanation performance with a CO2 conversion of high than 84% and 100% CH4 selectivity at a low temperature of 300 degrees C. A 100 h-on-stream test at 300 degrees C demonstrated the excellent stability of Ni/CeO2-P. Even when the WHSV rose as high as 30000 mL g(-1) h(-1), the Ni/CeO2-P catalyst still possessed a maximum CO2 conversion of approximately 79%. The surface characterization demonstrated that the abundant oxygen vacancies on the CeO2 nanoplates led to more amounts of NiO-CeO2 structures formed, which resulted in a stronger interaction between Ni metal and CeO2 support. This stronger NiO-CeO2 interaction was proved extraordinary in promoting the reaction performance as compared with metallic Ni. Also, by the in-situ DRIFTS technology, the reaction intermediates and possible reaction pathway were raised for CO2 methanation.
引用
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页数:10
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