Competition between insertion of Li+ and Mg2+: An example of TiO2-B nanowires for Mg rechargeable batteries and Li+/Mg2+ hybrid-ion batteries

被引:78
作者
Meng, Yuan [1 ]
Wang, Dashuai [1 ]
Wei, Yingjin [1 ]
Zhu, Kai [1 ]
Zhao, Yingying [1 ]
Bian, Xiaofei [1 ]
Du, Fei [1 ]
Liu, Bingbing [2 ]
Gao, Yu [1 ]
Chen, Gang [1 ,2 ]
机构
[1] Jilin Univ, Coll Phys, Minist Educ, Key Lab Phys & Technol Adv Batteries, Changchun 130012, Peoples R China
[2] Jilin Univ, State Key Lab Superhard Mat, Changchun 130012, Peoples R China
基金
中国国家自然科学基金;
关键词
Titanium dioxide bronze; Positive electrode; Magnesium ion battery; Hybrid-ion battery; First-principles calculations; Electrochemical properties; MAGNESIUM BOROHYDRIDE/TETRAGLYME ELECTROLYTE; TOTAL-ENERGY CALCULATIONS; WAVE BASIS-SET; AB-INITIO; STRUCTURAL-ANALYSIS; TITANIUM-DIOXIDE; CATHODE MATERIAL; LITHIUM; ANODE; PERFORMANCE;
D O I
10.1016/j.jpowsour.2017.02.033
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
Titanium dioxide bronze (TiO2-B) nanowires were prepared by the hydrothermal method and used as the positive electrode for Mg rechargeable batteries and Li+/Mg2+ hybrid-ion batteries. First-principles calculations showed that the diffusion barrier for Mg2+ (0.6 eV) in the TiO2-B lattice was more than twice of that for Li+ (0.3 eV). Electrochemical impedance spectroscopy showed that the charge transfer resistance of TiO2-B in the Mg2+ ion electrolyte was much larger than that in the Li+/Mg2+ hybrid electrolyte. For these reasons, the Mg rechargeable battery showed a small discharge capacity of 35 mAh g(-1) resulting from an electrochemical double-layer capacitive process. In comparison, the TiO2-B nanowires exhibited a large capacity (242 mAh g(-1) at the 20 mA g(-1) current density), high rate capability (114 mAh g(-1) at 1 A g(-1)), and excellent cycle stability in the Li+/Mg2+ hybrid-ion battery. The dominant reaction occurred in the TiO2-B electrode was intercalation of Li+ ions, of which about 74% of the total capacity was attributed to Li+ pseudo-capacitance. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:134 / 142
页数:9
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