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Boosting the hydrogen storage performance of magnesium hydride with metal organic framework-derived Cobalt@Nickel oxide bimetallic catalyst

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【作者】 Yan ZhangJiaguang ZhengZhiyu LuMengchen SongJiahuan HeFuying WuLiuting Zhang

【Author】 Yan Zhang;Jiaguang Zheng;Zhiyu Lu;Mengchen Song;Jiahuan He;Fuying Wu;Liuting Zhang;School of Energy and Power, Jiangsu University of Science and Technology;State Key Laboratory of Silicon Materials, Department of Materials Science and Engineering, Zhejiang University;Analysis and Testing Center, Jiangsu University of Science and Technology;

【通讯作者】 Jiaguang Zheng;Fuying Wu;Liuting Zhang;

【机构】 School of Energy and Power, Jiangsu University of Science and TechnologyState Key Laboratory of Silicon Materials, Department of Materials Science and Engineering, Zhejiang UniversityAnalysis and Testing Center, Jiangsu University of Science and Technology

【摘要】 In this study,a MOF-derived bimetallic Co@NiO catalyst was synthesized and doped into MgH2 to improve the hydrogen desorption and resorption kinetics.The Co@NiO catalyst decreased the onset dehydrogenation temperature of MgH2 by 160℃,compared with un-doped MgH2.The MgH2+9%(mass)Co@NiO composite released 6.6%(mass) hydrogen in 350 s at 315℃ and uptook 5.4%(mass) hydrogen in500 s at 165℃,showing greatly accelerated de/rehydrogenation rates.Besides,the desorption activation energy of MgH2+9%(mass) Co@NiO was decreased to(93.8±8.4) kJ·mol-1.Noteworthy,symbiotic Mg2NiH4/Mg2CoH5 clusters were in-situ formed from bimetallic precursors and inlaid on MgH2 surface,which are considered as "multi-step hydrogen pumps",and provides surface pathways for hydrogen absorption.Meanwhile,the introduced Mg2NiH4/Mg2CoH5 interfaces could provide numerous low energy barrier H diffusion channels,therefore accelerating the hydrogen release and uptake.This research proposes new insights to design high-efficiency bimetallic catalyst for MgH2 hydrogen storage.

【Abstract】 In this study,a MOF-derived bimetallic Co@NiO catalyst was synthesized and doped into MgH2 to improve the hydrogen desorption and resorption kinetics.The Co@NiO catalyst decreased the onset dehydrogenation temperature of MgH2 by 160℃,compared with un-doped MgH2.The MgH2+9%(mass)Co@NiO composite released 6.6%(mass) hydrogen in 350 s at 315℃ and uptook 5.4%(mass) hydrogen in500 s at 165℃,showing greatly accelerated de/rehydrogenation rates.Besides,the desorption activation energy of MgH2+9%(mass) Co@NiO was decreased to(93.8±8.4) kJ·mol-1.Noteworthy,symbiotic Mg2NiH4/Mg2CoH5 clusters were in-situ formed from bimetallic precursors and inlaid on MgH2 surface,which are considered as "multi-step hydrogen pumps",and provides surface pathways for hydrogen absorption.Meanwhile,the introduced Mg2NiH4/Mg2CoH5 interfaces could provide numerous low energy barrier H diffusion channels,therefore accelerating the hydrogen release and uptake.This research proposes new insights to design high-efficiency bimetallic catalyst for MgH2 hydrogen storage.

【基金】 financial supports from the National Natural Science Foundation of China(51801078);the Natural Science Foundation of Jiangsu Province(BK20210884)
  • 【文献出处】 Chinese Journal of Chemical Engineering ,中国化学工程学报(英文版) , 编辑部邮箱 ,2022年12期
  • 【分类号】TQ426
  • 【下载频次】1
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