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Although zinc oxide (ZnO) has a high theoretical capacity for lithium storage, its poor cyclability due to the huge volume changes during charge–discharge cycles result in particle pulverization and detachment from the current collector. In this work, a novel anode architecture for Li-ion batteries is fabricated by encapsulating ZnO nanoparticles in the hollow core of glassy carbon–reduced graphene oxide (C–rGO) electrospun composite nanofibers. A one-step, co-axial electrospinning method is used to synthesize a mat of core–shell structured composite nanofibers composed of rGO embedded in poly(acrylonitrile) (shell) and a ZnO nanoparticle precursor with a carrier polymer (core). Subsequent calcination and carbonization produce a mechanically stable anode material, which is used directly as a free-standing anode without any binder and current collector. The ZnO–C–rGO nanofiber composite was characterized by SEM, TEM, RAMAN and XRD techniques. The electrochemical performance of the composite was studied by galvanostatic charge–discharge measurements at different current densities, slow scan cyclic voltammetry (CV) and impedance measurements. Incorporation of an rGO network in the glassy nanofiber shell enhances both the capacity and electrical conductivity of the mat electrode resulting in faster electron kinetics, and thus, an improved rate capability. The interior void spaces combined with the mechanical strength and flexibility of the C–rGO shell act as a structural buffer effectively relieving the volumetric stresses generated during charge–discharge cycles. The synergistic effect of the metal oxide, rGO and the core–shell design results in a high capacity of 815mAh/g at a current density of 50mA/g with a capacity retention of almost 80% after 100 cycles, thus demonstrating significant potential as an anode substitute for next generation Li-ion batteries. |
