4-(Trifluoromethyl)-benzonitrile: A novel electrolyte additive for lithium nickel manganese oxide cathode of high voltage lithium ion battery

被引:95
|
作者
Huang, Wenna [1 ]
Xing, Lidan [1 ]
Wang, Yating [1 ]
Xu, Mengqing [1 ]
Li, Weishan [1 ]
Xie, Fengchao [2 ]
Xia, Shengan [2 ]
机构
[1] S China Normal Univ, Minist Educ,Sch Chem & Environm, Engn Res Ctr Mat & Technol Elect Energy Storage, Key Lab Elect Technol Energy Storage & Power Gene, Guangzhou 510006, Guangdong, Peoples R China
[2] Huawei Technol Co Ltd, Watt Lab, Shenzhen 518129, Peoples R China
基金
中国国家自然科学基金;
关键词
4-(Trifluoromethyl)benzonitrile; Electrolyte additive; Cyclic stability; High voltage lithium ion battery; SULFONE-BASED ELECTROLYTES; OXIDATIVE DECOMPOSITION; SPINEL LINI0.5MN1.5O4; PERFORMANCE; TEMPERATURE; CARBONATE; DINITRILE; SULFOLANE; LIQUID;
D O I
10.1016/j.jpowsour.2014.05.124
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
In this work, 4-(Trifluoromethyl)-benzonitrile (4-TB) is used as a novel electrolyte additive for LiNi0.5Mn1.5O4 cathode of high voltage lithium ion battery. Charge-discharge tests show that the cyclic stability of LiNi0.5Mn1.5O4 is significantly improved by using 0.5 wt.% 4-TB. With using 4-TB, LiNi0.5Mn1.5O4 delivers an initial capacity of 133 mAh g(-1) and maintains 121 mAh g(-1) after 300 cycles with a capacity retention of 91%, compared to the 75% of that using base electrolyte (1 M LiPF6 in ethylene carbonate(EC)/dimethyl carbonate(DMC)). The results from linear sweep voltammetry, density functional theory calculations, electrochemical impedance spectroscopy, scanning electron microscope, energy dispersive spectroscopy, Fourier transform infrared, and inductively coupled plasma, indicate that 4-TB has lower oxidative stability than EC and DMC, and is preferentially oxidized on LiNi0.5Mn1.5O4 forming a low-impedance protective film, which prevents the subsequent oxidation decomposition of the electrolyte and suppresses the manganese dissolution from LiNi0.5Mn1.5O4. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:560 / 565
页数:6
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