Synthesis of Mn3O4/N-doped graphene hybrid and its improved electrochemical performance for lithium-ion batteries

Mn₃O₄/N-doped graphene (Mn₃O₄/NG) hybrids were synthesized by a simple one-pot hydrothermal process. The scanning electron microscopy (SEM), transition electron microscopy (TEM), X-ray powder diffraction (XRD), Thermogravimetric analysis (TG), Raman Spectroscopy and X-ray photoelectron spectroscopy (XPS) were used to characterize the microstructure, crystallinity and compositions. It is demonstrated that Mn₃O₄ nanoparticles are high-dispersely anchored onto the individual graphene nanosheets, and also found that, in contrast with pure Mn₃O₄ obtained without graphene added, the introduction of graphene effectively restricts the growth of Mn₃O₄ nanoparticles. Simultaneously, the anchored well-dispersed Mn₃O₄ nanoparticles also play a role as spacers in preventing the restacking of graphene sheets and producing abundant nanoscale porous channels. Hence, it is well anticipated that the accessibility and reactivity of electrolyte molecules with Mn₃O₄/NG electrode are highly improved during the electrochemical process. As the anode material for lithium ion batteries, the Mn₃O₄/NG hybrid electrode displays an outstanding reversible capacity of 1208.4 mAh g^?1 after 150 cycles at a current density of 88 mA g^?1, even still retained 284 mAh g^?1 at a high current density of 4400 mA g^?1 after 10 cycles, indicating the superior capacity retention, which is better than those of bare Mn₃O₄, and most other Mn₃O₄/C hybrids in reported literatures. Finally, the superior performance can be ascribed to the uniformly distribution of ultrafine Mn₃O₄ nanoparticles, successful nitrogen doping of graphene and favorable structures of the composites.