阳极
材料科学
电化学
锂(药物)
化学工程
热解炭
电极
碳化
铁
电导率
复合数
纳米技术
化学
扫描电子显微镜
复合材料
冶金
热解
工程类
内分泌学
物理化学
医学
作者
Min Li,Wensheng Ma,Fuquan Tan,Bin Yu,Guanhua Cheng,Hui Gao,Zhonghua Zhang
标识
DOI:10.1016/j.jpowsour.2023.233146
摘要
Magnetite (Fe3O4) has become a potential anode material in lithium ion batteries (LIBs) because of its high theoretical capacity and low cost, but is impeded for application by its low conductivity and large volume change during cycling. Herein, the Fe3O4@C-500 composite was fabricated via the one-step pyrolytic carbonization of commercial ammonium ferric citrate (AFC), which is simple and environmentally friendly. As an anode in LIBs, the Fe3O4@C-500 electrode shows superior specific capacity, long cycling stability and excellent rate performance. Such remarkable performance can be attributed to the formation of the architecture with carbon (C) matrix, not only buffering the volume change and inhibiting the aggregation of internal Fe3O4 nanoparticles during (de)lithiation, but also elevating the electron conductivity. In situ X-ray diffraction (XRD) results demonstrate that the (de)lithiated mechanism of the Fe3O4@C-500 electrode involves a full electrochemically-driven amorphization upon cycling. Furthermore, the full cell assembled with Fe3O4@C-500 and LiFePO4 (LFP) electrodes shows outstanding electrochemical performance, demonstrating its practical energy storage application.
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