Improved lithium storage performance of lithium sodium titanate anode by titanium site substitution with aluminum

被引:29
|
作者
Wang, Pengfei [1 ,2 ]
Li, Peng [1 ]
Yi, Ting-Feng [2 ]
Lin, Xiaoting [1 ]
Zhu, Yan-Rong [2 ]
Shao, Lianyi [1 ]
Shui, Miao [1 ]
Long, Nengbing [1 ]
Shu, Jie [1 ]
机构
[1] Ningbo Univ, Fac Mat Sci & Chem Engn, Ningbo 315211, Zhejiang, Peoples R China
[2] Anhui Univ Technol, Sch Chem & Chem Engn, Maanshan 243002, Anhui, Peoples R China
基金
中国国家自然科学基金;
关键词
Lithium-ion batteries; Anode material; Lithium sodium titanate; Metal doping; Electrochemical property; EQUAL-TO; 0.2; ELECTROCHEMICAL PERFORMANCE; DOPED LI4TI5O12; MLI2TI6O14; M; BA; SRLI2TI6O14; BATTERIES; OXIDE; SR;
D O I
10.1016/j.jpowsour.2015.05.076
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
Li2Na2Ti6O14 and its Ti-site substitution Li2Na2Ti5.9M0.1O14 (M = Al, Zr, V) are prepared by a solid-state reaction method and used as anode materials for lithium-ion batteries. It is found that metal doping can effectively enhance the electronic conductivity and ionic diffusion coefficient of Li2Na2Ti6O14. Especially for Li2Na2Ti5.9Al0.1O14, it reveals the highest electronic conductivity (1.02 x 10(-9) S cm(-1)) and lithium ion diffusion coefficient (8.38 x 10(-15) cm(2) s(-1)) among all the samples. As a result, Li2Na2Ti5.9Al0.1O14 reveals the best electrochemical performance. It can deliver a charge specific capacity of 270.3 mAh g(-1) at 50 mA g(-1). Even cycled at 1000 mA g(-1), it still can present a charge capacity of 180.7 mAh g(-1). All these enhanced lithium storage capabilities of Li2Na2Ti5.9Al0.1O14 should be attributed to the increased electronic/ionic conductivities and the decreased charge transfer resistance induced by Al doping. Besides, in-situ X-ray diffraction observation also confirms that the structural change of Li2Na2Ti5.9Al0.1L14 is highly reversible process for lithium storage. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:33 / 41
页数:9
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