材料科学
阳极
电极
异质结
锂(药物)
纳米技术
电解质
化学工程
同轴
离子
纳米颗粒
阴极
光电子学
医学
量子力学
电气工程
物理
工程类
内分泌学
物理化学
化学
作者
Desheng Li,Yu Zhang,Kun Rui,Huijuan Lin,Yan Yan,Xiaoshan Wang,Chao Zhang,Xiao Huang,Jixin Zhu,Wei Huang
出处
期刊:Nanotechnology
[IOP Publishing]
日期:2018-12-11
卷期号:30 (9): 094002-094002
被引量:9
标识
DOI:10.1088/1361-6528/aaf7c5
摘要
Nanostructured manganese oxides have been regarded as promising anodes for lithium-ion batteries (LIBs) due to their high specific capacity, environmental friendliness and low cost. However, as conversion-type electrodes, their scalable utilization is hindered by intrinsically low reaction kinetics, large volume variation and high polarization. Herein, a coaxial-cable tubular heterostructure composed of a hollow carbon skeleton, Fe3O4 nanoparticles and ultrathin MnO2 nanosheets from inside out, donated as MnO2@Fe3O4@C, is synthesized via a facile two-step hydrothermal process. The unique design integrates conductive carbon and nanostructured MnO2 and Fe3O4 into a one-dimensional (1D) hierarchically open architecture, which provides abundant electrode-electrolyte contact areas, favorable heterointerfaces and ultrafast electron/ion pathways. Benefiting from these features, the MnO2@Fe3O4@C anode exhibits a high reversible capacity of 946 mAh g-1 at 200 mA g-1 after 160 cycles, and excellent cyclability with a specific capacity of 845 mAh g-1 at 500 mA g-1 after 600 cycles. This work might provide an insightful guideline for the design of novel electrode materials.
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