Effect of solid electrolyte interface (SEI) film on cyclic performance of Li4Ti5O12 anodes for Li ion batteries

被引:245
作者
He, Yan-Bing [1 ]
Liu, Ming [2 ]
Huang, Zhen-Dong [1 ]
Zhang, Biao [1 ]
Yu, Yang [1 ]
Li, Baohua [2 ]
Kang, Feiyu [2 ]
Kim, Jang-Kyo [1 ]
机构
[1] Hong Kong Univ Sci & Technol, Dept Mech Engn, Kowloon, Hong Kong, Peoples R China
[2] Tsinghua Univ, Grad Sch Shenzhen, Key Lab Thermal Management Engn & Mat, Shenzhen 518055, Peoples R China
关键词
Lithium titanate; Solid electrolyte interface; Surface morphology; Vinylene carbonate; ELECTROCHEMICAL PERFORMANCE; LITHIUM STORAGE; SPINEL LI4TI5O12; RATE CAPABILITY; IMPEDANCE; INSERTION; GRAPHITE; ADDITIVES; SPECTROSCOPY; TEMPERATURE;
D O I
10.1016/j.jpowsour.2013.03.141
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
Understanding the formation of SEI films on Li4Ti5O12 (LTO) anodes offers a major benefit to large-scale applications of lithium ion batteries made therefrom. This paper reveals that an SEI film is formed above 1 V due to the interfacial reaction between the electrode and electrolyte: LTO anodes are previously considered free from SEI films when cycled between 1 and 3 V. The reactivity and the formation of SEI films are much affected by the morphology and surface area of the electrode. To study the above, LTO powders with different morphologies are synthesized using lithium acetate (LA) and lithium hydroxide (LH) as the lithium sources. LTO-LH consisting of agglomerates of primary small particles with a large surface area has higher reactivity than LTO-LA with a cubic structure and small surface area. As a result, the LTO-LH anode with a smooth SEI film offers better cyclic performance than the LTO-LA anode with a porous SEI film. The addition of vinylene carbonate to the electrolyte facilitates rapid formation of a protective SEI film on LTO LA, greatly improving the rate and cyclic performance: stable specific capacity of 155.6 mAh g(-1) and remarkable 135.2 mAh g(-1) after 500 cycles at 10 C are recorded. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:269 / 276
页数:8
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