Co@SiO 2 /C catalyst shielded by hierarchical shell for robust hydrogen production
Applied Catalysis B: Environmental, ISSN: 0926-3373, Vol: 343, Page: 123537
2024
- 7Citations
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
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Article Description
NaBH 4 hydrolysis under mild conditions is a promising solution for mobile hydrogen applications. However, the design and synthesis of cost-effective catalysts with sufficiently high activity and stability remain challenging. Herein, we report a facile approach to construct a series of SiO 2 shielding cobalt-based catalysts with hierarchical active sites. Under optimized conditions, the hydrogen productivity of 18% Co@SiO 2 /C-300 is 8-fold higher than 18% Co/C catalyst without SiO 2 shell. The incorporation of SiO 2 shell enhances the partial oxidation of Co nanoparticles, resulting in the formation of a mesosphere CoO x overlayer covered by a SiO 2 shell on Co particles. Meanwhile, the cobalt oxide on Co NPs could remain stable under reductive reaction conditions. The unique structural and electronic properties of the Co@SiO 2 /C configuration is demonstrated to enhance the activation of NaBH 4 and H 2 O and promote H 2 desorption, giving rise to a higher level of inherent activity and a relatively low reaction energy barrier.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S0926337323011803; http://dx.doi.org/10.1016/j.apcatb.2023.123537; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85177866344&origin=inward; https://linkinghub.elsevier.com/retrieve/pii/S0926337323011803; https://dx.doi.org/10.1016/j.apcatb.2023.123537
Elsevier BV
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