High-loading, ultrafine Ni nanoparticles dispersed on porous hollow carbon nanospheres for fast (de)hydrogenation kinetics of MgH2

Magnesium hydride (MgH2) is one of the most promising hydrogen storage materials for practical application due to its favorable reversibility, low cost and environmental benign; however, it suffers from high dehydrogenation temperature and slow sorption kinetics. Exploring proper catalysts with high...

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Main Authors: Shun Wang, Mingxia Gao, Zhihao Yao, Kaicheng Xian, Meihong Wu, Yongfeng Liu, Wenping Sun, Hongge Pan
Format: Article
Language:English
Published: KeAi Communications Co., Ltd. 2022-12-01
Series:Journal of Magnesium and Alloys
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S2213956721001225
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author Shun Wang
Mingxia Gao
Zhihao Yao
Kaicheng Xian
Meihong Wu
Yongfeng Liu
Wenping Sun
Hongge Pan
author_facet Shun Wang
Mingxia Gao
Zhihao Yao
Kaicheng Xian
Meihong Wu
Yongfeng Liu
Wenping Sun
Hongge Pan
author_sort Shun Wang
collection DOAJ
description Magnesium hydride (MgH2) is one of the most promising hydrogen storage materials for practical application due to its favorable reversibility, low cost and environmental benign; however, it suffers from high dehydrogenation temperature and slow sorption kinetics. Exploring proper catalysts with high and sustainable activity is extremely desired for substantially improving the hydrogen storage properties of MgH2. In this work, a composite catalyst with high-loading of ultrafine Ni nanoparticles (NPs) uniformly dispersed on porous hollow carbon nanospheres is developed, which shows superior catalytic activity towards the de-/hydrogenation of MgH2. With an addition of 5 wt% of the composite, which contains 90 wt% Ni NPs, the onset and peak dehydrogenation temperatures of MgH2 are lowered to 190 and 242 °C, respectively. 6.2 wt% H2 is rapidly released within 30 min at 250 °C. The amount of H2 that the dehydrogenation product can absorb at a low temperature of 150 °C in only 250 s is very close to the initial dehydrogenation value. A dehydrogenation capacity of 6.4 wt% remains after 50 cycles at a moderate cyclic regime, corresponding to a capacity retention of 94.1%. The Ni NPs are highly active, reacting with MgH2 and forming nanosized Mg2Ni/Mg2NiH4. They act as catalysts during hydrogen sorption cycling, and maintain a high dispersibility with the help of the dispersive role of the carbon substrate, leading to sustainably catalytic activity. The present work provides new insight into designing stable and highly active catalysts for promoting the (de)hydrogenation kinetics of MgH2.
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spelling doaj.art-d89c03e0d7d9471b9f45cb4b616629232024-04-28T06:37:44ZengKeAi Communications Co., Ltd.Journal of Magnesium and Alloys2213-95672022-12-01101233543366High-loading, ultrafine Ni nanoparticles dispersed on porous hollow carbon nanospheres for fast (de)hydrogenation kinetics of MgH2Shun Wang0Mingxia Gao1Zhihao Yao2Kaicheng Xian3Meihong Wu4Yongfeng Liu5Wenping Sun6Hongge Pan7State Key Laboratory of Silicon Materials, Key Laboratory of Advanced Materials and Applications for Batteries of Zhejiang Province & School of Materials Science and Engineering, Zhejiang University, Hangzhou 310027, P.R. ChinaCorresponding author.; State Key Laboratory of Silicon Materials, Key Laboratory of Advanced Materials and Applications for Batteries of Zhejiang Province & School of Materials Science and Engineering, Zhejiang University, Hangzhou 310027, P.R. ChinaState Key Laboratory of Silicon Materials, Key Laboratory of Advanced Materials and Applications for Batteries of Zhejiang Province & School of Materials Science and Engineering, Zhejiang University, Hangzhou 310027, P.R. ChinaState Key Laboratory of Silicon Materials, Key Laboratory of Advanced Materials and Applications for Batteries of Zhejiang Province & School of Materials Science and Engineering, Zhejiang University, Hangzhou 310027, P.R. ChinaState Key Laboratory of Silicon Materials, Key Laboratory of Advanced Materials and Applications for Batteries of Zhejiang Province & School of Materials Science and Engineering, Zhejiang University, Hangzhou 310027, P.R. ChinaState Key Laboratory of Silicon Materials, Key Laboratory of Advanced Materials and Applications for Batteries of Zhejiang Province & School of Materials Science and Engineering, Zhejiang University, Hangzhou 310027, P.R. ChinaState Key Laboratory of Silicon Materials, Key Laboratory of Advanced Materials and Applications for Batteries of Zhejiang Province & School of Materials Science and Engineering, Zhejiang University, Hangzhou 310027, P.R. ChinaCorresponding author.; State Key Laboratory of Silicon Materials, Key Laboratory of Advanced Materials and Applications for Batteries of Zhejiang Province & School of Materials Science and Engineering, Zhejiang University, Hangzhou 310027, P.R. ChinaMagnesium hydride (MgH2) is one of the most promising hydrogen storage materials for practical application due to its favorable reversibility, low cost and environmental benign; however, it suffers from high dehydrogenation temperature and slow sorption kinetics. Exploring proper catalysts with high and sustainable activity is extremely desired for substantially improving the hydrogen storage properties of MgH2. In this work, a composite catalyst with high-loading of ultrafine Ni nanoparticles (NPs) uniformly dispersed on porous hollow carbon nanospheres is developed, which shows superior catalytic activity towards the de-/hydrogenation of MgH2. With an addition of 5 wt% of the composite, which contains 90 wt% Ni NPs, the onset and peak dehydrogenation temperatures of MgH2 are lowered to 190 and 242 °C, respectively. 6.2 wt% H2 is rapidly released within 30 min at 250 °C. The amount of H2 that the dehydrogenation product can absorb at a low temperature of 150 °C in only 250 s is very close to the initial dehydrogenation value. A dehydrogenation capacity of 6.4 wt% remains after 50 cycles at a moderate cyclic regime, corresponding to a capacity retention of 94.1%. The Ni NPs are highly active, reacting with MgH2 and forming nanosized Mg2Ni/Mg2NiH4. They act as catalysts during hydrogen sorption cycling, and maintain a high dispersibility with the help of the dispersive role of the carbon substrate, leading to sustainably catalytic activity. The present work provides new insight into designing stable and highly active catalysts for promoting the (de)hydrogenation kinetics of MgH2.http://www.sciencedirect.com/science/article/pii/S2213956721001225Hydrogen storage materialsNano-catalysisMagnesium hydridePorous hollow carbon nanospheresNi nanoparticles
spellingShingle Shun Wang
Mingxia Gao
Zhihao Yao
Kaicheng Xian
Meihong Wu
Yongfeng Liu
Wenping Sun
Hongge Pan
High-loading, ultrafine Ni nanoparticles dispersed on porous hollow carbon nanospheres for fast (de)hydrogenation kinetics of MgH2
Journal of Magnesium and Alloys
Hydrogen storage materials
Nano-catalysis
Magnesium hydride
Porous hollow carbon nanospheres
Ni nanoparticles
title High-loading, ultrafine Ni nanoparticles dispersed on porous hollow carbon nanospheres for fast (de)hydrogenation kinetics of MgH2
title_full High-loading, ultrafine Ni nanoparticles dispersed on porous hollow carbon nanospheres for fast (de)hydrogenation kinetics of MgH2
title_fullStr High-loading, ultrafine Ni nanoparticles dispersed on porous hollow carbon nanospheres for fast (de)hydrogenation kinetics of MgH2
title_full_unstemmed High-loading, ultrafine Ni nanoparticles dispersed on porous hollow carbon nanospheres for fast (de)hydrogenation kinetics of MgH2
title_short High-loading, ultrafine Ni nanoparticles dispersed on porous hollow carbon nanospheres for fast (de)hydrogenation kinetics of MgH2
title_sort high loading ultrafine ni nanoparticles dispersed on porous hollow carbon nanospheres for fast de hydrogenation kinetics of mgh2
topic Hydrogen storage materials
Nano-catalysis
Magnesium hydride
Porous hollow carbon nanospheres
Ni nanoparticles
url http://www.sciencedirect.com/science/article/pii/S2213956721001225
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