石墨烯-氧化膜CoP2@C阳极实现高容量锂离子电池

Wei Zhang, Hangxuan Xie, Zirui Dou, Zhentao Hao, Qianhui Huang, Ziqi Guo, Chao Wang, Kanghua Miao, Xiongwu Kang
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引用次数: 0

摘要

二磷化钴(CoP2)具有较高的理论容量,作为锂离子电池(LIBs)的负极材料具有广阔的应用前景。然而,在锂离子的插入和提取过程中,CoP2的体积和结构发生了很大的变化,导致电极破碎,固体电解质界面受损,最终导致循环性能不佳。本文通过co - mof基沸石咪唑盐框架(ZIF-67)的碳化和顺序磷酸化,成功地合成了包裹在碳基体中的CoP2纳米颗粒复合材料,并进一步包裹在氧化石墨烯(CoP2@C@GO)中。通过x射线衍射、高分辨率透射电镜和x射线光电子能谱证实了CoP2的形成。通过扫描电镜和透射电子能谱分析了CoP2@C包覆和未包覆氧化石墨烯的形貌。结果表明,氧化石墨烯的修饰显著降低了CoP2@C电极的极化,提高了其充电容量和循环稳定性。经过200次循环后,它们提供450 mAh·g−1的容量。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Graphene-Oxide-Coated CoP2@C Anode Enables High Capacity of Lithium-Ion Batteries
Cobalt diphosphides (CoP2) show a high theoretical capacity and hold great promise as anode materials for lithium-ion batteries (LIBs). However, the large variation in the volume and structure of CoP2 caused during lithium-ion insertion and extraction results in electrode fragmentation and a compromised solid electrolyte interface, ultimately leading to poor cycling performance. Herein, a composite of CoP2 nanoparticles encapsulated in carbon matrix has been successfully synthesized by carbonization of Co-MOF-based zeolitic imidazolate frameworks (ZIF-67) and sequential phosphorization and further wrapped in graphene oxide (CoP2@C@GO). The formation of CoP2 was confirmed by X-ray diffraction, high-resolution transmission electron microscopy and X-ray photoelectron spectroscopy. The morphology of CoP2@C with and without GO wrapping was examined by scanning electron microscopy and transmission electron spectroscopy. It was demonstrated that the decoration of GO significantly reduces the polarization of CoP2@C electrodes, enhancing their charge capacity and cycling stability as an anode material for LIBs. After 200 cycles, they deliver a capacity of 450 mAh·g−1.
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