Abstract:Thermally oxidized MWCNTs (OMWCNTs) are fabricated by a thermal treatment of MWCNTs at 500℃ for 3 h in an oxygen-containing atmosphere. The oxygen content of OMWCNTs increases from 1.9 wt.% for MWCNTs to 8.3 wt.%. And the BET specific surface area of OMWCNTs enhances from 254.2 m2 g-1 for MWCNTs to 496.1 m2 g-1. The Fe2O3/OMWCNTs nanocomposite is prepared by a hydrothermal method. Electrochemical measurements show that Fe2O3/OMWCNTs still keeps a highly reversible specific capacity of 653.6 mA h g-1 after 200 … Show more
“…Therefore, developing substituted anode materials with more excellent electrochemical performance have become the focus of attention. Transition metal oxides (TMOs) [5], such as Fe 2 O 3 [6][7][8][9], Fe 3 O 4 [10], TiO 2 [11], and Co 3 O 4 [7], have much higher theoretical specific capacity than graphite by conversion reaction mechanisms (M x O y + 2yLi + + 2ye − = XM0 + yLi 0 ) [12], which are considered as potential candidate materials for LIBs anode. Among all kinds of TMOs, Fe 2 O 3 has drawn considerable attention, owing to its high theoretical capacity (1007 mAh g −1 ), non-toxicity, high natural abundance, low cost, etc [13,14].…”
The development of Fe2O3 as lithium-ion batteries (LIBs) anode is greatly restricted by its poor electronic conductivity and structural stability. To solve these issues, this work presents in situ construction of three-dimensional crumpled Fe2O3@N-Ti3C2Tx composite by solvothermal-freeze-drying process, in which wormlike Fe2O3 nanoparticles (10 ~ 50 nm) in situ nucleated and grew on the surface of N-doped Ti3C2Tx nanosheets with Fe-O-Ti bonding. As a conductive matrix, N-doping endows Ti3C2Tx with more active sites and higher electron transfer efficiency. Meanwhile, Fe-O-Ti bonding enhances the stability of the Fe2O3/N-Ti3C2Tx interface and also acts as a pathway for electron transmission. With a large specific surface area (114.72 m2 g-1), the three-dimensional crumpled structure of Fe2O3@N-Ti3C2Tx facilitates the charge diffusion kinetics and enables easier exposure of the active sites. Consequently, Fe2O3@N-Ti3C2Tx composite exhibits outstanding electrochemical performance as anode for LIBs, a reversible capacity of 870.2 mAh g-1 after 500 cycles at 0.5 A g-1, 1129 mAh g-1 after 280 cycles at 0.2 A g-1 and 777.6 mAh g-1 after 330 cycles at 1 A g-1.
“…Therefore, developing substituted anode materials with more excellent electrochemical performance have become the focus of attention. Transition metal oxides (TMOs) [5], such as Fe 2 O 3 [6][7][8][9], Fe 3 O 4 [10], TiO 2 [11], and Co 3 O 4 [7], have much higher theoretical specific capacity than graphite by conversion reaction mechanisms (M x O y + 2yLi + + 2ye − = XM0 + yLi 0 ) [12], which are considered as potential candidate materials for LIBs anode. Among all kinds of TMOs, Fe 2 O 3 has drawn considerable attention, owing to its high theoretical capacity (1007 mAh g −1 ), non-toxicity, high natural abundance, low cost, etc [13,14].…”
The development of Fe2O3 as lithium-ion batteries (LIBs) anode is greatly restricted by its poor electronic conductivity and structural stability. To solve these issues, this work presents in situ construction of three-dimensional crumpled Fe2O3@N-Ti3C2Tx composite by solvothermal-freeze-drying process, in which wormlike Fe2O3 nanoparticles (10 ~ 50 nm) in situ nucleated and grew on the surface of N-doped Ti3C2Tx nanosheets with Fe-O-Ti bonding. As a conductive matrix, N-doping endows Ti3C2Tx with more active sites and higher electron transfer efficiency. Meanwhile, Fe-O-Ti bonding enhances the stability of the Fe2O3/N-Ti3C2Tx interface and also acts as a pathway for electron transmission. With a large specific surface area (114.72 m2 g-1), the three-dimensional crumpled structure of Fe2O3@N-Ti3C2Tx facilitates the charge diffusion kinetics and enables easier exposure of the active sites. Consequently, Fe2O3@N-Ti3C2Tx composite exhibits outstanding electrochemical performance as anode for LIBs, a reversible capacity of 870.2 mAh g-1 after 500 cycles at 0.5 A g-1, 1129 mAh g-1 after 280 cycles at 0.2 A g-1 and 777.6 mAh g-1 after 330 cycles at 1 A g-1.
Three main iron oxides, FeO, Fe2O3, and Fe3O4, have attracted much attention as anode materials for lithium-ion batteries (LIBs) for their high theoretical capacity, low cost, large-scale reserves, and environmental benignity. However, the poor cycling life and rate capability limit their commercial application on a large scale. Glaring strategies have been adopted to improve the performance of lithium storage. In this review, the electrochemical performances of FeO, Fe2O3, and Fe3O4 anode materials could be improved by the decrease in particle size, regulation and control of the nanomicrostructures, the improvement of electrical conductivity, and the design of composites. Their effects on the electrochemical performance of the anode materials are discussed in detail. Furthermore, the development prospect of iron oxide-basedanode material has been prospected.
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