Carbonyl oxygen-coordinated metallic cobalt nanoparticles anchored on hybrid mesoporous silica matrix to enhance 4-nitrophenol hydrogenation

被引：10

作者：

Huo, Hang ^{[1
]}

Jiang, Yanqiu ^{[1
]}

Wang, Zhe ^{[1
]}

Hu, Yanjing ^{[1
]}

Zhao, Tingting ^{[1
]}

Liu, Xing ^{[1
]}

Xu, Xianzhu ^{[1
]}

Lin, Kaifeng ^{[1
]}

机构：

[1] Harbin Inst Technol, MIIT Key Lab Crit Mat Technol New Energy Convers, Sch Chem & Chem Engn, Harbin 150001, Heilongjiang, Peoples R China

来源：

JOURNAL OF MATERIALS SCIENCE | 2021年 / 56卷 / 01期

基金：

中国国家自然科学基金;

关键词：

FISCHER-TROPSCH SYNTHESIS; N-DOPED CARBON; CATALYTIC-ACTIVITY; PARTICLE-SIZE; DISPERSION; REDUCTION; CO3O4; ELECTROCATALYST; IMPACT; OXIDE;

D O I：

10.1007/s10853-020-05263-5

中图分类号：

T [工业技术];

学科分类号：

08 ;

摘要：

In this paper, urea group functionalized periodic mesoporous organosilica was utilized as matrix to introduce cobalt precursor into framework. After pyrolysis in nitrogen atmosphere, urea group was decomposed into carbon species and simultaneously the cobalt precursor was reduced to metallic cobalt nanoparticles. The metallic cobalt nanoparticles can be stabilized by coordinating to carbonyl oxygen atoms in carbon species. The supported metallic cobalt exhibited excellent catalytic performance towards 4-nitrophenol hydrogenation reaction. The largest turnover frequency number can reach up to 164.8 h(-1), and the reaction rate constant can be as high as 0.77 min(-1). The influence of pyrolysis temperature on catalytic performance was also investigated. Compared with the results obtained by samples prepared with wet impregnation method or different pyrolysis rate, it can be concluded that the coordination to carbonyl oxygen atom in carbon species plays a crucial role in improving electron transfer between metallic cobalt and carbon species during catalytic procedure.

引用

页码：364 / 379

页数：16

共 49 条

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