TiO2 nanotube arrays annealed in CO exhibiting high performance for lithium ion intercalation

被引:105
作者
Liu, Dawei [1 ]
Zhang, Yunhuai [1 ,2 ]
Xiao, Peng [3 ]
Garcia, Betzaida Batalla [1 ]
Zhang, Qifeng [1 ]
Zhou, Xiaoyuan [1 ]
Jeong, Yoon-Ha [4 ]
Cao, Guozhong [1 ]
机构
[1] Univ Washington, Dept Mat Sci & Engn, Seattle, WA 98195 USA
[2] Chongqing Univ, Dept Chem Engn, Chongqing, Peoples R China
[3] Chongqing Univ, Dept Phys, Chongqing, Peoples R China
[4] Pohang Univ Sci & Technol, NCNT, Pohang, South Korea
基金
美国国家科学基金会;
关键词
Li ion intercalation; TiO2 nanotube arrays; CO annealing; Point defects; Charge-transfer; DIOXIDE NANOWALL ARRAYS; ANODE MATERIAL; ELECTROCHEMICAL PROPERTIES; NATURAL GRAPHITE; PARTICLE-SIZE; ANATASE; BATTERIES; CAPACITY; TITANIUM; ELECTRODES;
D O I
10.1016/j.electacta.2009.06.090
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Anatase titania nanotube arrayswere fabricated by means of anodization of Ti foil and annealed at 400 degrees C in respective CO and N-2 gases for 3 h. Electrochemical impendence spectroscopy study showed that CO annealed arrays possessed a noticeably lower charge-transfer resistance as compared with arrays annealed in N-2 gas under otherwise the same conditions. TiO2 nanotube arrays annealed in CO possessed much improved lithium ion intercalation capacity and rate capability than N-2 annealed samples. At a high charge/discharge current density of 320 mA g(-1), the initial discharge capacity in CO annealed arrays was found to be as high as 223 mAh g(-1), 30% higher than N-2 annealed arrays, similar to 164 mAh g(-1). After 50 charge/discharge cycles, the discharge capacity in CO annealed arrays remained at similar to 179 mAh g(-1). The improved intercalation capacity and rate capability could be attributed to the presence of surface defects like Ti-C species and Ti3+ groups with oxygen vacancies, which not only improved the charge-transfer conductivity of the arrays but also possibly promoted phase transition. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:6816 / 6820
页数:5
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