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Ti-V-Ni合金
INTERNATIONAL JOURNAL OF HYDROGEN ENERGY · 2014 ·Vol. 39 ·期 7 ·3313-3319 · IF 2.93

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

Jing Lin,Fei Liang,Yaoming Wu,Wanqiang Liu,Limin Wang

We prepared Ti 1.4 V 0.6 Ni ribbons by arc-melting and subsequent melt-spinning techniques. Ti 1.4 V 0.6 Ni +  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. Ti 1.4 V 0.6 Ni +  x Mg composite alloys contained icosahedral quasicrystalline phase, Ti 2 Ni-type phase, β-Ti solid-solution phase and metallic Mg. The electrochemical and gaseous hydrogen storage properties of alloys were improved with Mg addition. Ti 1.4 V 0.6 Ni + 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 Ti 1.4 V 0.6 Ni +  x Mg ( x  = 1, 2 and 3, wt.%) alloys were better than Ti 1.4 V 0.6 Ni. Ti 1.4 V 0.6 Ni + 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.

研究领域: 材料科学 · 金属功能材料 · 储能材料 · 物理化学 · 电化学
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JOURNAL OF ALLOYS AND COMPOUNDS · 2017 · IF 3.133

Improved electrochemical performance of Ti1.4V0.6Ni hydrogen storage alloy in its composite with LiAlH4

Jing Lin,Zhanyi Cao,Lianshan Sun,Fei Liang,Limin Wang

Ti 1.4 V 0.6 Ni +  x LiAlH 4 ( x  = 0.5, 1, 1.5, 2, 2.5, wt.%) composites were prepared by ball-milling, and the effects of LiAlH 4 content on structure and electrochemical properties of the composites were investigated systematically. The addition of LiAlH 4 to the Ti 1.4 V 0.6 Ni alloy significantly affected the morphology and size of the composite particles . The electrochemical cycling stability and rate dischargeability of the composite electrodes benefitted from adding some LiAlH 4 ( x  = 1), which however deteriorated when the LiAlH 4 content increased further. The positive effect of LiAlH 4 on the electrochemical performance of the studied alloy was caused by suppression of the dissolution of active components of the Ti 1.4 V 0.6 Ni hydrogen storage alloy.

研究领域: 材料科学 · 金属功能材料 · 能源存储 · 电化学 · 氢能技术
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