Abstract

Fe 2 O 3 are attractive anode materials for lithium-ion batteries because of their large theoretical capacity and low cost. However, due to their low conductivity, large volume variation and unstable solid electrolyte interface (SEI), their cycling stability is poor. Herein, we developed a simple and general strategy to address these issues. The well-designed yolk-shell Fe 2 O 3 @C nanospheres with the inner Fe 2 O 3 nanoparticles are protected by highly-graphitized and interconnected carbon shells prepared by oxidizing commercial acetylene black. The obtained yolk-shell Fe 2 O 3 @C nanospheres provide sufficient interior void to buffer the volumetric variation of the inner Fe 2 O 3 nanoparticles during cycling. Furthermore, the highly-graphitized and perforated mesoporous carbon shells facilitate fast electron transfer and ions transportation during the charge/discharge process. Benefiting from these structural advantages, the yolk-shell Fe 2 O 3 @C nanospheres provide good cyclic stability which still retain 929 mAh g −1 after 200 cycles at the current density of 0.1 A g −1 and elevate Li + diffusion coefficient from 3.867 × 10 −13 to 6.321 × 10 −11 m 2 s −1 . This work provides a new perspective to design the yolk-shell metal oxides@C framework for exploring the high-performance Li-ion batteries. • Acetylene blacks was constructed into hollow carbon nanospheres. • Unique chain structure and high graphitization degree of carbon shell provides an effective conductive network. • The obtained yolk-shell Fe 2 O 3 @C nanospheres provide sufficient interior void to buffer the volumetric variation of the inner Fe 2 O 3 nanoparticles during cycling. • Fe 2 O 3 @C still retain 929 mAh g −1 after 200 cycles and the Li + diffusion coefficient goes from 3.867 × 10 −13 to 6.321 × 10 −11 m 2 s −1 .

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