摘要
Though great progresses have been made on improving the volume effect and electronic conductivity of anode materials in sodium-ion batteries (SIBs), the electrical performance at high current density for long cycling stability is still a huge challenge. To address this, a facile confined-impregnation/crystallization strategy is developed to construct a movable Fe2O3 core in nitrogen-doped hierarchical porous carbon nanospheres (MFe2O3@N-HCNs) for ultrafast intercalation/deintercalation of SIBs. The as-prepared MFe2O3@N-HCNs not only exhibit a connected and hierarchal porous structure with large surface specific area (∼367 m2 g–1) but also possess a highly dispersed and moveable Fe2O3 core (∼5 nm) for the tolerance of volume expansion during the intercalation/deintercalation process of sodium ions. As SIBs anode materials, the MFe2O3@N-HCNs anode exhibits a capacity of 417 mAh g–1 at 0.1 A g–1 after 100 cycles and of 364 mAh g–1 at 2 A g–1 with 4500 cycles. Especially, a prominent discharge capacity of 102 mAh g–1 is still obtained at 5 A g–1 after 10000 cycles. Such remarkable performances should be attributed to the unique highly dispersed and moveable Fe2O3 core and conductive nitrogen-doped hierarchical porous carbon framework with large surface area. Consequently, this study develops a facile methodology to promote the energy storage and long cycling performance of hierarchically porous carbon@transition-metal oxide (TMO) composite anode materials for SIBs, especially at high current density.
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