标题:One-step hydrothermal synthesis of ZnFe2O4 nano-octahedrons as a high capacity anode material for Li-ion batteries
作者:Xing, Zheng; Ju, Zhicheng; Yang, Jian; Xu, Huayun; Qian, Yitai
作者机构:[Xing Zheng] Department of Chemistry, University of Science and Technology of China, Hefei National Laboratory for Physical Sciences at Microscale, He 更多
通讯作者:Ju, Z(juzc@ustc.edu.cn)
通讯作者地址:[Ju, ZC]Univ Sci & Technol China, Hefei Natl Lab Phys Sci Microscale, Hefei 230026, Anhui, Peoples R China.
来源:纳米研究
出版年:2012
卷:5
期:7
页码:477-485
DOI:10.1007/s12274-012-0233-2
关键词:Hydrothermal method; ZnFe2O4 octahedrons; Li-ion batteries; anode; materials; rate performance
摘要:Binary transition metal oxides are considered as promising anode materials for lithium-ion batteries (LIB), because they can effectively overcome the drawbacks of simple oxides. Here, a one-step hydrothermal method is described for the synthesis of regular ZnFe2O4 octahedrons about 200 nm in size at a low temperature without further annealing being required. The ZnFe2O4 octahedrons were characterized by powder X-ray diffraction, scanning electron microscopy, high-resolution transmission electron microscopy and X-ray photoelectron spectroscopy. The electrochemical performance of the ZnFe2O4 octahedrons was examined in terms of cyclic voltammetry and discharge/charge profiles. The ZnFe2O4 octahedrons exhibit a high capacity of 910 mA center dot h/g at 60 mA/g between 0.01 and 3.0 V after 80 cycles. They also deliver a reversible specific capacity of 730 mA center dot h/g even after 300 cycles at 1000 mA/g, a much better performance than those in previous reports. A set of reactions involved in the discharge/charge processes are proposed on the basis of ex situ high-resolution transmission electron microscopy (HRTEM) images and selected area electron diffraction (SAED) patterns of the electrode materials. The insights obtained will be of benefit in the design of future anode materials for lithium ion batteries.
收录类别:CSCD;SCOPUS;SCIE
WOS核心被引频次:155
Scopus被引频次:157
资源类型:期刊论文
原文链接:https://www.scopus.com/inward/record.uri?eid=2-s2.0-84864131266&doi=10.1007%2fs12274-012-0233-2&partnerID=40&md5=912ae2ab2d80b4ad1e748f3e7076b58e
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