High density Co₃O₄ nanoparticles confined in a porous graphene nanomesh network driven by an electrochemical process: ultra-high capacity and rate performance for lithium ion batteries
2013
Zhu, Xiao | Ning, Guoqing | Ma, Xinlong | Fan, Zhuangjun | Xu, Chenggen | Gao, Jinsen | Xu, Chunming | Wei, Fei
Here, we report a novel Co₃O₄–graphene hybrid electrode material with high density Co₃O₄ nanoparticles (NPs) in a size range of 2–3 nm confined in a few-layered porous graphene nanomesh (PGN) framework driven by an electrochemical process. Raman spectra indicate that Co species preferentially anchor on the defective sites of the PGN, which results in markedly reduced irreversible Li storage and therefore significantly enhanced coulombic efficiency. The ultra-small Co₃O₄ NPs provide a large surface area and a short solid-state diffusion length, which is propitious to achieving a high Li ion capacity at high rate. Also, the few-layered graphene network with high electronic conductivity not only permits easy access to the high surface area of the Co₃O₄ NPs for the electrolyte ions, but also serves as a reservoir for high capacity Li storage. As a result, the Co₃O₄–PGN composite layers deliver an ultra-high capacity (1543 mA h g⁻¹ at 150 mA g⁻¹) and excellent rate capability (1075 mA h g⁻¹ at 1000 mA g⁻¹) with good cycling stability.
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