Hydrogen storage properties of Ti1.4V0.6Ni + x Mg (x=1-3, wt.%) alloys

被引:19
|
作者
Lin, Jing [1 ]
Mang, Fei [1 ,3 ]
Wu, Yaoming [1 ,3 ]
Liu, Wanqiang [2 ]
Wang, Limin [1 ,3 ]
机构
[1] Chinese Acad Sci, Changchun Inst Appl Chem, State Key Lab Rare Earth Resource Utilizat, Changchun 130022, Peoples R China
[2] Changchun Univ Sci & Technol, Sch Mat Sci & Engn, Changchun 130022, Peoples R China
[3] Changzhou Inst Energy Storage Mat & Devices, Changzhou 213000, Peoples R China
基金
国家高技术研究发展计划(863计划); 中国国家自然科学基金;
关键词
Ti-based quasicrystalline; Magnesium; Composite alloy; Hydrogen storage property; ELECTROCHEMICAL PROPERTIES; TI-ZR; DIFFRACTION; PHASE;
D O I
10.1016/j.ijhydene.2013.12.059
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
We prepared Ti1.4V0.6Ni ribbons by arc-melting and subsequent melt-spinning techniques. Ti1.4V0.6Ni + x Mg (x = 1, 1.5, 2, 2.5 and 3, wt.%) composite alloys were obtained by the mechanical ball-milling method. The structures and hydrogen storage properties of alloys were investigated. Ti1.4V0.6Ni + x Mg composite alloys contained icosahedral quasicrystalline phase, Ti2Ni-type phase, beta-Ti solid-solution phase and metallic Mg. The electrochemical and gaseous hydrogen storage properties of alloys were improved with Mg addition. Ti1.4V0.6Ni + 2 Mg alloy showed maximum electrochemical discharge capacity of 282.5 mAh g(-1) as well as copacetic high-rate discharge ability of 82.3% at the discharge current density of 240 mA g(-1) compared with that of 30 mA g(-1), and the cycling life achieved above 200 mAh g(-1) after 50 consecutive cycles of charging and discharging. The hydrogen absorption/desorption properties of Ti1.4V0.6Ni + x Mg (x = 1, 2 and 3, wt.%) alloys were better than Ti1.4V0.6Ni. Ti1.4V0.6Ni + 3 Mg alloy also exhibited a favorable hydrogen absorption capacity of 1.53 wt.%. The improvement in the hydrogen storage characteristics caused by adding Mg may be ascribed to better hydrogen diffusion and anti-corrosion ability. Copyright (C) 2013, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:3313 / 3319
页数:7
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