阳极
石墨烯
材料科学
X射线光电子能谱
电化学
电导率
锂(药物)
氧化还原
离子
化学工程
纳米技术
化学
电极
冶金
物理化学
医学
有机化学
内分泌学
工程类
作者
Wenwen Wang,Hongyun Cui,Jiwen Cui,Tong Wang,Jingquan Sha,Guodong Liu
标识
DOI:10.1016/j.jallcom.2023.171817
摘要
Even being promising anode materials for lithium-ion batteries (LIBs), Co3O4 is still hindered by poor redox and large volume change during dis-/charging. Herein, series of PW12@Co3O4@GO composites were successfully fabricated to address the aforementioned shortcomings by pinning monodispersed H3PW12O40 (PW12) on Co3O4 and then coating graphene (GO). Results of X-ray photoelectron spectroscopy (XPS) and cyclic voltammograms (CV) show that PW12 was successfully anchored to the macromolecule Co3O4 by covalent Co-O-W bond, where, to improve the ion and charge transfer rate of Co3O4, the excellent ionic conductivity and multi-electron redox of PW12 as “Li+ migration entrance” were explored for the first time, meanwhile, the capacity retention of PW12 was greatly maintained (97.5% after 250 cycles). Moreover, GO as electronic conductor and buffer improves the overall conductivity and copes with large volume changes of Co3O4, which ensures the capacity retention rate of PW12@Co3O4@GO-2 of 94.9% after 250 cycles. Finally, we delved into the lithium storage process and proposed a possible lithium storage mechanism of PW12@Co3O4@GO-2, which provides a new insight to trigger the electrochemical activity for next-generation anode materials.
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