材料科学
阳极
碳化
合金
储能
碳纤维
电化学
纳米技术
化学工程
复合数
电导率
电极
芯(光纤)
复合材料
化学
物理化学
扫描电子显微镜
工程类
物理
功率(物理)
量子力学
作者
Tianqi Gao,Yizhuo Song,Lijun Xie,Xiaojun Zhao,Zhi‐Hong Liu
标识
DOI:10.1016/j.jallcom.2023.168911
摘要
The applications of metal chalcogenides in Li/Na-ion storage are limited by their low intrinsic conductivity and structure pulverization, which result in capacity reduction and low-rate performance. To overcome these limitations, herein, a core-shell box structure consisting of Fe3Se4 and Co7Fe3 alloying compound integrated with N, Se-doped carbon core and N, Se-doped carbon shell (denoted as Fe3Se4/CoFe/[email protected]) is fabricated successfully using an initial selenization/carbonization and subsequent thermal induction strategy of the corresponding hollow CoFe-Prussian Blue analogue box precursor. The possible formation mechanism of Fe3Se4/CoFe/[email protected] is proposed. The core-shell Fe3Se4/CoFe/[email protected] with the void space can accommodate the volume expansion and facilitate Li+/Na+ dissolusion on cycling, while the resulting Co7Fe3 alloy compound and NSeC can synergistically accelerate the conductivity of the electrode material from local and overall aspects for rapid electron and ion transportation. As a result, the Fe3Se4/CoFe/[email protected] box anode exhibits superior electrochemical performance in both LIBs and SIBs, such as a reversible specific capacity of 976.6 mAh g−1 at 0.2 A g−1 and even 782.5 mAh g−1 at 1 A g−1 for LIBs, and 324 mAh g−1 at 0.2 A g−1 for SIBs, respectively. The improved Li/Na storage properties of the composite demonstrate the significance of meticulously constructing novel multicomponent hierarchical structures with higher complexity.
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