Facile synthesized Fe nanosheets as superior active catalyst for hydrogen storage in MgH2

被引:136
作者
Zhang, Liuting [1 ]
Ji, Liang [1 ]
Yao, Zhendong [3 ]
Yan, Nianhua [1 ]
Sun, Ze [1 ]
Yang, Xinglin [1 ]
Zhu, Xinqiao [2 ]
Hu, Shuanglin [2 ]
Chen, Lixin [3 ]
机构
[1] Jiangsu Univ Sci & Technol, Sch Energy & Power, Zhenjiang 212003, Jiangsu, Peoples R China
[2] China Acad Engn Phys, Inst Nucl Phys & Chem, Mianyang 621999, Sichuan, Peoples R China
[3] Zhejiang Univ, Dept Mat Sci & Engn, Hangzhou 310027, Zhejiang, Peoples R China
基金
美国国家科学基金会; 中国国家自然科学基金;
关键词
Hydrogen storage; Magnesium hydride; Fe nanosheet; Catalytic effect; Ab initio calculation; TOTAL-ENERGY CALCULATIONS; NANOPARTICLES; KINETICS; PERFORMANCE; DESORPTION; GRAPHENE; DEHYDROGENATION; THERMODYNAMICS; IMPROVEMENT; MECHANISMS;
D O I
10.1016/j.ijhydene.2019.06.065
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Reversible hydrogen storage in MgH2 under mild conditions is a promising way for the realization of "Hydrogen Economy", in which the development of cheap and highly efficient catalysts is the major challenge. Herein, A two-dimensional layered Fe is prepared via a facile wet-chemical ball milling method and has been confirmed to greatly enhance the hydrogen storage performance of MgH2. Minor addition of 5 wt% Fe nanosheets to MgH2 decreases the onset desorption temperature to 182.1 degrees C and enables a quick release of 5.44 wt% H-2 within 10 min at 300 degrees C. Besides, the dehydrogenated sample takes up 6 wt% H-2 in 10 min under a hydrogen pressure of 3.2 MPa at 200 degrees C. With the doping of Fe nano sheets, the apparent activation energy of the dehydrogenation reaction for MgH2 is reduced to 40.7 +/- 1.0 kJ mol(-1). Further ab initio calculations reveal that the presence of Fe extends the Mg-H bond length and reduces its bond strength. We believe that this work would shed light on designing plain metal for catalysis in the area of hydrogen storage and other energy-related issues. (C) 2019 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:21955 / 21964
页数:10
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