The CeO2 morphology modulates the density and catalytic performance of dual-active site for enhancing the palmitic acid conversion

被引:0
作者
Xin, Hui [1 ]
Chen, Xilei [2 ]
Xiao, Cuncun [2 ]
Chao, Jun [2 ]
Zhang, Hualong [2 ]
Tan, Jiwei [2 ]
Hu, Changwei [2 ]
Wu, Lan [1 ]
Li, Dan [2 ]
机构
[1] Sichuan Univ, Analyt & Testing Ctr, Chengdu 610064, Sichuan, Peoples R China
[2] Sichuan Univ, Coll Chem, Key Lab Green Chem & Technol, Minist Educ, Chengdu 610064, Sichuan, Peoples R China
基金
中国国家自然科学基金;
关键词
Cerium oxide; Morphology; Nickel; Dual-active site; Palmitic acid; OXYGEN VACANCIES; CO2; WATER; CERIA; REACTIVITY; OXIDATION; NI/CEO2; HYDRODEOXYGENATION; HYDROGENATION; DEOXYGENATION;
D O I
10.1016/j.fuel.2024.132890
中图分类号
TE [石油、天然气工业]; TK [能源与动力工程];
学科分类号
0807 ; 0820 ;
摘要
Designing active sites with multi-function to meet the complicated reaction is a challenge task. Herein, we find that morphology of cerium oxide (CeO2) shows strong influence on the density and catalytic reactivity of dual-active site formed on it. Nanorods CeO2 (CeO2-NR) has large specific surface area and abundant oxygen vacancy (O-v), making small size of Ni (below 2 nm) highly disperse on it. However, 39.7 nm Ni poorly distributes on CeO2 composed of irregularly stacked particles (CeO2-NP), displaying much smaller specific surface area and fewer O-v compared with those on CeO2-NR. Small size Ni and abundant O-v show better abilities in activation of H-2 and palmitic acid, respectively. Moreover, abundant O-v and highly dispersed Ni increase their intimacy on CeO2-NR. These make Ni/CeO2-NR catalyst has high density of Ni-O-v dual-active site, showing better synergetic catalytic performance for conversion of palmitic acid into alkanes than that on Ni/CeO2-NP.
引用
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页数:9
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