Enhancing Li-ion battery anode performances via disorder/order engineering

被引:87
作者
Zhang, Yanfei [1 ]
Wang, Peixing [1 ]
Zheng, Tian [1 ]
Li, Deming [1 ]
Li, Guangda [1 ]
Yue, Yuanzheng [1 ,2 ,3 ]
机构
[1] Qilu Univ Technol, Shandong Acad Sci, Sch Mat Sci & Engn, Jinan 250353, Shandong, Peoples R China
[2] Aalborg Univ, Dept Chem & Biosci, DK-9220 Aalborg, Denmark
[3] Wuhan Univ Technol, State Key Lab Silicate Mat Architectures, Wuhan 430070, Hubei, Peoples R China
基金
中国国家自然科学基金;
关键词
Li-ion battery; Anode; Disorder/order engineering; Nanocrystals; RECHARGEABLE LITHIUM BATTERIES; GLASS-CERAMICS; ELECTROCHEMICAL PERFORMANCE; HIGH-CAPACITY; ELECTRODES; CONDUCTIVITY; OXIDE; CRYSTALLIZATION; NANOPARTICLES; NANOMATERIALS;
D O I
10.1016/j.nanoen.2018.05.018
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
The performance of the anode materials is critical to further development of Li-ion batteries. However, the cycling stability and safety performance of anode materials are still far from satisfying. Here we propose a new strategy, i.e., the disorder/order engineering, by which the anode performance of the Li-ion battery can be improved. First, the disordered materials were prepared by vitrifying V2O5-TeO2 (VT) liquids, and then the VT glass powder was mixed with acetylene black and binder to form anode for a lithium ion battery. Second, by subjecting the battery to discharging/charging cycles, the VT glass was partially transformed into ordered phases at the nanoscale, i.e., the disorder-order transition occurred. Even the first cycle of discharging/charging induced the disorder-order transition. The ordered nano-domains and the disordered matrix exert a synergetic effect to facilitate the ionic and electronic transport and to maintain structure stable against discharging/charging. As a consequence, both the capacity and the cycling stability were greatly enhanced, and the structural origin of such enhancement was explored. This study has opened a new way for developing high performance anodes for Li-ion batteries.
引用
收藏
页码:596 / 602
页数:7
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