Abstract:The flourish of insertion reaction-type V 2 O 3 negative materials with large reversible capacity and outstanding rate performance is facing a huge trouble. In this study, we have successfully prepared a V 2 O 3 @C/rGO composite by adjusting surface tension. The small V 2 O 3 @C nanosheets are fastened to reduced graphene oxide, which remarkably elevates the electron and lithium ion transfer rate. More importantly, the obvious interaction between V 2 O 3 and reduced graphene oxide is beneficial for faster char… Show more
“…Reducing the particle size is an effectual strategy. Smaller particle size can help diminish the volume variation in the Li + insertion and release process and shorten the lithium ion diffusion distance. − Integrating SnO 2 with N-doped carbon is another effectual strategy, which can further dramatically mute the volume variation in the Li + insertion and release process and quicken the lithium ion and electron transfer speed. − Introducing an appropriate amount of Sn is also an effectual strategy to suppress the volume change in the lithium insertion and release process and improve cyclic stability, − which could be interpreted by the two-stage electrochemical reaction process of SnO 2 : a conversion process (converting SnO 2 into Sn) and an alloying process of Sn. During the conversion reaction stage, the introduced Sn can be a buffer for volume change; in the alloying reaction stage, the formed Li 2 O in the first stage can also relieve the volume change and protects active materials from aggregating.…”
The development of SnO 2 -based negative materials possessing a long cyclic life is troubled by their huge volume change in the Li + insertion and detachment process. In our study, the SnO 2 /Sn/NC composite was successfully prepared by an uncomplicated and controllable route. The ultrasmall SnO 2 /Sn nanoparticles are fixed on the N-doped carbon framework, which prominently alleviate its vast volume variation and improve its electrochemical reaction kinetics. The above-mentioned feature of SnO 2 /Sn/NC endows it with an exceptional cyclic lifespan and good rate capability. When employed as the negative electrode for the Li-ion battery at 1.0 A g −1 , it releases a competent discharge capacity of 344 mAh g −1 at the 995th cycle. New dawn would be brought by the investigation of the synthesis and utilization of Sn-based compounds.
“…Reducing the particle size is an effectual strategy. Smaller particle size can help diminish the volume variation in the Li + insertion and release process and shorten the lithium ion diffusion distance. − Integrating SnO 2 with N-doped carbon is another effectual strategy, which can further dramatically mute the volume variation in the Li + insertion and release process and quicken the lithium ion and electron transfer speed. − Introducing an appropriate amount of Sn is also an effectual strategy to suppress the volume change in the lithium insertion and release process and improve cyclic stability, − which could be interpreted by the two-stage electrochemical reaction process of SnO 2 : a conversion process (converting SnO 2 into Sn) and an alloying process of Sn. During the conversion reaction stage, the introduced Sn can be a buffer for volume change; in the alloying reaction stage, the formed Li 2 O in the first stage can also relieve the volume change and protects active materials from aggregating.…”
The development of SnO 2 -based negative materials possessing a long cyclic life is troubled by their huge volume change in the Li + insertion and detachment process. In our study, the SnO 2 /Sn/NC composite was successfully prepared by an uncomplicated and controllable route. The ultrasmall SnO 2 /Sn nanoparticles are fixed on the N-doped carbon framework, which prominently alleviate its vast volume variation and improve its electrochemical reaction kinetics. The above-mentioned feature of SnO 2 /Sn/NC endows it with an exceptional cyclic lifespan and good rate capability. When employed as the negative electrode for the Li-ion battery at 1.0 A g −1 , it releases a competent discharge capacity of 344 mAh g −1 at the 995th cycle. New dawn would be brought by the investigation of the synthesis and utilization of Sn-based compounds.
Synergistic regulation of hierarchical nanostructures and defect engineering is effective in accelerating electron and ion transport for metal oxide electrodes. Herein, carbon nanofiber‐supported V2O3 with enriched oxygen vacancies (OV‐V2O3@CNF) was fabricated using the facile electrospinning method, followed by thermal reduction. Differing from the traditional particles embedded within carbon nanofibers or irregularly distributed between carbon nanofibers, the free‐standing OV‐V2O3@CNF allows for V2O3 nanosheets to grow vertically on one‐dimensional (1D) carbon nanofibers, enabling abundant active sites, shortened ion diffusion pathway, continuous electron transport, and robust structural stability. Meanwhile, density functional theory calculations confirmed that the oxygen vacancies can promote intrinsic electron conductivity and reduce ion diffusion energy barrier. Consequently, the OV‐V2O3@CNF anode delivers a large reversible capacity of 812 mAh g−1 at 0.1 A g−1, superior rate capability (405 mAh g−1 at 5 A g−1), and long cycle life (378 mAh g−1 at 5 A g−1 after 1000 cycles). Moreover, an all‐vanadium full battery (V2O5//OV‐V2O3@CNF) was assembled using an OV‐V2O3@CNF anode and a V2O5 cathode, which outputs a working voltage of 2.5 V with high energy density and power density, suggesting promising practical application. This work offers fresh perspectives on constructing hierarchical 1D nanofiber electrodes by combining defect engineering and electrospinning technology.
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