Effect of Li on electrochemical properties of Ti1.4V0.6Ni quasicrystal alloy produced by rapid quenching

被引:4
|
作者
Ouyang, Zhongtao [1 ]
Liu, Kun [1 ]
Shang, Jinming [1 ]
Xing, Cheng [1 ]
Liu, Wanqiang [1 ]
Wang, Limin [2 ]
机构
[1] Changchun Univ Sci & Technol, Sch Mat Sci & Engn, Changchun 130022, Peoples R China
[2] Chinese Acad Sci, Changchun Inst Appl Chem, State Key Lab Rare Earth Resource Utilizat, Changchun 130022, Peoples R China
关键词
Electrochemistry; Hydrogen storage; Rapid solidification; Electrochemical characterization; HYDROGEN STORAGE CAPACITY; ICOSAHEDRAL PHASE;
D O I
10.1016/j.intermet.2015.03.010
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
The effect of Li on the electrochemical performance of electrodes consisting of Ti1.4V0.6Ni quasicrystal was investigated at room temperature in three-electrode cell set-up. The quasicrystal sample was initially synthesized by arc melting, followed by melt-spinning, and then infiltrated with Li atoms by electroosmosis. According to X-ray diffraction, all ribbon samples were determined to be icosahedral quasicrystal phase (I-phase), V-based solid solution phase with BCC structure and face centered cubic (FCC) phase with Ti2Ni-type structure. After infiltrating some Li atoms into the Ti1.4V0.6Ni quasicrystal lattice under the condition of an electroosmosis current of 0.6 A, we could observe the appearance of Li diffraction peaks. Importantly, the slight shift to the left observed in the diffraction peaks indicated that lattice expansion was caused by the infiltration of Li. The discharge capacity of Ti1.4V0.6Ni-Li material was higher than that of Ti1.4V0.6Ni.The maximum discharge capacity of 307.1 mAh/g was recorded for Ti1.4V0.6Ni Li at a current density of 30 mAh/g. Both high-rate dischargeability and cycling stability were enhanced as a result of infiltrating Li. The lithium could get into the lattice, which resulted in the formation of microspores on surface of alloy, thus improving electrochemical activity of the alloy electrode. At the same time, the electrochemical reaction kinetics of alloy electrodes was also researched. (C) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:50 / 55
页数:6
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