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

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Abstract

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.

Graphic abstract

Metallic cobalt nanoparticles with high dispersion were introduced into urea group functionalized mesoporous silica matrix via pyrolysis in nitrogen atmosphere. The coordination to carbonyl oxygen atom enhances the catalytic performance in 4-nitrophenol hydrogenation.

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Acknowledgements

This work was financially supported by the National Natural Science Foundation of China (granted number: 51472062) and the Opening Project of key Laboratory of Polyoxometalate Science of Ministry of Education of China. The authors greatly acknowledge the financial support.

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Correspondence to Yanqiu Jiang or Kaifeng Lin.

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Huo, H., Jiang, Y., Wang, Z. et al. Carbonyl oxygen-coordinated metallic cobalt nanoparticles anchored on hybrid mesoporous silica matrix to enhance 4-nitrophenol hydrogenation. J Mater Sci 56, 364–379 (2021). https://doi.org/10.1007/s10853-020-05263-5

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