Recent advancement of SiOx, based anodes for lithium-ion batteries

被引:365
作者
Chen, Tao [1 ,4 ]
Wu, Ji [2 ]
Zhang, Qinglin [1 ,5 ]
Su, Xin [3 ]
机构
[1] Univ Kentucky, Dept Chem & Mat Engn, Lexington, KY 40506 USA
[2] Georgia Southern Univ, Dept Chem, Statesboro, GA 30458 USA
[3] Eagle Picher Technol, Joplin, MO 64802 USA
[4] BAK Battery Co Ltd, Shenzhen 518119, Guangdong, Peoples R China
[5] Gen Motors Global Res & Dev Ctr, Warren, MI 48375 USA
基金
美国国家科学基金会;
关键词
Lithium-ion batteries; SiOx; Si; Anode; SOLID-ELECTROLYTE INTERPHASE; HIGH-PERFORMANCE ANODE; NITROGEN-DOPED CARBON; MONOXIDE NEGATIVE ELECTRODE; AMORPHOUS-SILICON MONOXIDE; ELECTRICAL ENERGY-STORAGE; LI-ION; HIGH-CAPACITY; ELECTROCHEMICAL PERFORMANCE; VINYLENE CARBONATE;
D O I
10.1016/j.jpowsour.2017.07.073
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
Si monoxide and its suboxides (SiOx) are promising anode materials for lithium-ion batteries which have attracted special attention recently due to its high specific capacity and improved cycling performance, with some similarities to Si anodes. While Li oxide (Li2O) and Li silicates (Li4SiO4), generated by the reaction of Li ion with SiOx during the first lithiation process lowers the theoretical capacity, they also act as buffer components to accommodate volume changes caused by further reactions between Si in SiOx with Li, leading to improved cyclability. One of the main drawbacks of this material is the low first cycle Coulombic efficiency due to the formation of the Li oxide and Li silicates. In this paper, the electrochemical properties and related mechanism of SiOx are reviewed. The current research progress to enhance SiOx electrochemical performance by nanostructuring and the effect of other battery components such as binders, electrolyte, and prelithiation on its electrochemical performance is also discussed. Finally, potential research directions and strategies to further improve the performance of SiOx are also briefly discussed and suggested. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:126 / 144
页数:19
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