Hierarchical porous Co-CoO@NC hollow microspheres with capacity growth by reactivation of solid-electrolyte interface films

Transition metal oxide (TMO)-based electrodes exhibit increased capacities, yet the mechanism behind the true cause of capacity in such materials remains unclear. Herein, hierarchical porous and hollow Co-CoO@NC spheres assembled by nanorods with refined nanoparticles and amorphous carbon have been synthesized by a two-step annealing approach. A temperature gradient-driven mechanism is revealed for the evolution of the hollow structure. Compared with the solid CoO@NC spheres, the novel hierarchical of Co-CoO@NC can fully utilize the interior active material by exposing both ends of each nanorod into electrolyte. The hollow interior provides extra space for the volume variation, leading to an up-trend capacity of 919.3 mAh g^-1 at 200 mA g^-1 over 200 cycles. Differential capacity curves disclose that solid electrolyte interface (SEI) films reactivation partly contributes to increasing reversible capacity. The introduction of nanosized Co particles benefits the process by participating in the transformation of SEI components. This study provides a guide for constructing anodic material with exceptional electrochemical performance.