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Research Article | Open Access

Graphene-Supported Sc2O3/TiO2 for Superior Catalysis on Hydrogen Sorption Kinetics of MgH2

Haixiang Huang1,2Jinting Chen1,2Tingting Xu1,2Yujie Lv1,2Bogu Liu1,2Bao Zhang2Jianguang Yuan2Ying Wu1,2( )
School of Energy, Power and Mechanical Engineering, North China Electric Power University, Beijing 102206, China
Institute of Energy Power Innovation, North China Electric Power University, Beijing 102206, China
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Abstract

Complex metal oxide catalysts greatly accelerate the hydrogen sorption rates in the magnesium hydride system. In this study, the graphene-supported Sc2O3/TiO2 catalyst is synthesized by means of a simple method, and a surprisingly synergetic effect of the Sc2O3-TiO2 cocatalyst on the hydrogen storage performance of MgH2 is observed. The MgH2-Sc2O3/TiO2@Gn composite starts to release hydrogen at 140 ℃ and reaches the peak dehydrogenation temperature at 239.9 ℃. It absorbs 6.55 wt% of H2 in 1 min and desorbs 5.71 wt% of H2 in 10 min at 300 ℃, showing excellent hydrogen absorption and desorption performance. Furthermore, with the decrease of the grain size and changes in the structure, the activity of the catalyst is greatly improved. The low-valent titanium and scandium and oxygen vacancies formed in the process of dehydrogenation facilitate hydrogen diffusion and electron transfer, and further improve the kinetic performance of the Mg/MgH2-Sc2O3/TiO2@Gn system. This study aims to provide insights into studying complex metal oxides as catalysts to improve hydrogen storage performance, and shed light on other catalysis-related research.

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Energy Material Advances
Article number: 0055

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Cite this article:
Huang H, Chen J, Xu T, et al. Graphene-Supported Sc2O3/TiO2 for Superior Catalysis on Hydrogen Sorption Kinetics of MgH2. Energy Material Advances, 2023, 4: 0055. https://doi.org/10.34133/energymatadv.0055

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Received: 17 July 2023
Accepted: 27 August 2023
Published: 22 September 2023
© 2023 Haixiang Huang et al. Exclusive licensee Beijing Institute of Technology Press. No claim to original U.S. Government Works.

Distributed under a Creative Commons Attribution License 4.0 (CC BY 4.0).