Non-aqueous electrodeposition of porous tin-based film as an anode for lithium-ion battery

被引:71
作者
Gu, C. D. [1 ]
Mai, Y. J.
Zhou, J. P.
You, Y. H.
Tu, J. P.
机构
[1] Zhejiang Univ, State Key Lab Silicon Mat, Hangzhou 310027, Peoples R China
基金
中国国家自然科学基金; 高等学校博士学科点专项科研基金;
关键词
Ionic liquid; Electrodeposition; Tin; Lithium-ion batteries; SITU X-RAY; ELECTROCHEMICAL PROPERTIES; SECONDARY BATTERIES; CHOLINE CHLORIDE; STORAGE CAPACITY; ALLOY ANODES; MOLTEN-SALT; LIQUIDS; LI; SN;
D O I
10.1016/j.jpowsour.2012.04.085
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
Porous tin-based films are electrodeposited on copper foils from a choline chloride/ethylene glycol based electrolyte containing SnCl2 center dot 2H(2)O without any complexing agent or additive. Increasing the deposition time and voltage produces thicker films. The initially deposited Sn grains are relatively uniform with an average size of 200-300 nm and a kind of self-assembly distribution constructing an open and bicontinuous porous network. The architecture of these films possesses a double-layer structure, i.e. SnO2 (superficial layer)/Sn-Cu alloy (bottom layer), which is revealed by X-ray diffractometer and X-ray photoelectron spectroscopy. The electrochemical performance of the porous tin-based films as anode for lithium-ion batteries is measured. Although the capacity fades gradually with repeated cycling, a reversible capacity of 300-350 mAh g(-1) is maintained for more than 50 cycles, which suggests that the in situ formed Sn-Cu alloy could provide an interlocking interface between active materials and current collector. Therefore, the tin's shedding from the current collector can be restrained. Moreover, the inactive materials, such as the oxide in the superficial layer and the Cu in the bottom layer, could also act as buffers to relieve the induced volume expansion of Sn during the repeated lithiathion/delithiation process, thus giving the good cycle performances. (c) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:200 / 207
页数:8
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