Controlling nanocrystallization and hydrogen storage property of Mg-based amorphous alloy via a gas-solid reaction

被引:51
|
作者
Lin, Huai-Jun [1 ,2 ,4 ]
Zhang, Chi [2 ]
Wang, Hui [2 ]
Ouyang, Liuzhang [2 ]
Zhu, Yunfeng [1 ,4 ]
Li, Liquan [1 ,4 ]
Wang, Weihua [3 ]
Zhu, Min [2 ]
机构
[1] Nanjing Tech Univ, Coll Mat Sci & Engn, 5 Xinmofan Rd, Nanjing 210009, Jiangsu, Peoples R China
[2] South China Univ Technol, Sch Mat Sci & Engn, Guangzhou 510640, Guangdong, Peoples R China
[3] Chinese Acad Sci, Inst Phys, Beijing 100080, Peoples R China
[4] Nanjing Tech Univ, Jiangsu Collaborat Innovat Ctr Adv Inorgan Funct, 5 Xinmofan Rd, Nanjing 210009, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
Hydrogen storage; Mg-based alloy; Nanocomposite; Crystallite size; Gas-solid reaction; IN-SITU SYNCHROTRON; X-RAY-DIFFRACTION; 1ST-ORDER PHASE-TRANSITIONS; MELT-SPUN; DESORPTION; KINETICS; NI; MAGNESIUM; THERMODYNAMICS; PARTICLES;
D O I
10.1016/j.jallcom.2016.05.286
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
A valid strategy via a gas-solid reaction for preparing Mg-based nanocomposite with controllable crystallite size and suitable for massive production is proposed. The nanocomposites consisting of well-dispersed catalytic nano-Mg2NiH4/CeH2.73 embedded in the nano-MgH2 matrix with crystallite sizes of all phases below 10 nm are fabricated via controlling activation temperature and hydrogen gas (H-2) pressure upon the amorphous Mg80Ce10Ni10 alloy. Increasing H2 pressure and reducing temperature are beneficial for obtaining fine hydrides, leading to lowered hydrogen desorption temperature. MgH2 and CeH2.73 gradually grow up with the increase of de-/re-hydrogenation cycles, while Mg2NiH4 remains stable during cycling. After 15 de-/re-hydrogenation cycles, the finest nanocomposite shows remarkably reduced activation energy of dehydrogenation of 87 +/- 7 kJ/mol (similar to 160 kJ/mol for commercial MgH2). (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:272 / 277
页数:6
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