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Wood-Derived Carbon Fibers Embedded with SnO x Nanoparticles as Anode Material for Lithium-Ion Batteries.

ABSTRACT: Carbon-SnO x composites are obtained by impregnating acetylacetone-treated, delignified wood fibers with tin precursor and successively carbonizing at 1000 °C in 95% argon and 5% oxygen. Scanning electron microscopy and nitrogen sorption studies (Brunauer-Emmett-Teller) show that acetylacetone treatment stabilizes the wood fiber structure during carbonization at 1000 °C and preserves the porous structural features. X-ray diffraction, transmission electron microscopy, and X-ray photoelectron spectroscopy studies show that the small amount of oxygen introduced in inert atmosphere passivates the surface of tin nanoparticles. The passivation process yields thermally and electrochemically stable SnO x particles embedded in carbon matrix. The resultant carbon-SnO x material with 16 wt% SnO x shows excellent electrochemical performance of rate capability from 0.1 to 10 A g-1 and cycling stability for 1000 cycles with Li-ion storage capacity of 280 mAh g-1 at a current density of 10 A g-1. The remarkable electrochemical performance of wood-derived carbon-SnO x composite is attributed to the reproduction of structural featured wood fibers to nanoscale in carbon-SnO x composite and controlled passivation of tin nanoparticles to yield SnO x nanoparticles.

SUBMITTER: Revathi J

PROVIDER: S-EPMC6957017 | biostudies-literature | 2020 Jan

REPOSITORIES: biostudies-literature

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Wood-Derived Carbon Fibers Embedded with SnO x Nanoparticles as Anode Material for Lithium-Ion Batteries.

Revathi Janardhanan J Jyothirmayi Adduru A Rao Tata Narasinga TN Deshpande Atul Suresh AS

Global challenges (Hoboken, NJ) 20191108 1

Carbon-SnO x composites are obtained by impregnating acetylacetone-treated, delignified wood fibers with tin precursor and successively carbonizing at 1000 °C in 95% argon and 5% oxygen. Scanning electron microscopy and nitrogen sorption studies (Brunauer-Emmett-Teller) show that acetylacetone treatment stabilizes the wood fiber structure during carbonization at 1000 °C and preserves the porous structural features. X-ray diffraction, transmission electron microscopy, and X-ray ...[more]

PMID: 31956425

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Project description:Bagasse-derived carbon electrodes were developed by doping with nitrogen functional groups and compositing with high-capacity MnO2 nanoparticles (MnO2/NBGC). The bagasse-derived biochar was N-doped by refluxing in urea, followed by the deposition of MnO2 nanoparticles onto its porous surface via the hydrothermal reduction of KMnO4. Different initial KMnO4 loading concentrations (i.e. 5, 10, 40, and 100 mM) were applied to optimize the composite morphology and the corresponding electrochemical performance. Material characterization confirmed that the carbon composite has a mesoporous structure along with the dispersion of MnO2 nano-particles on the N-containing carbon surface. It was found that the 5-MnO2/NBGC sample exhibited the highest electrochemical performance with a reversible capacity of 760 mA h g-1 at a current density of 186 mA g-1. It delivered reversible capacities of 488 and 390 mA h g-1 in cycle tests at 372 and 744 mA g-1, respectively, for 150 cycles and presented good reversibility with nearly 100% coulombic efficiency. In addition, it could exert high capacities up to 388 and 301 mA h g-1 even under high current densities of 1860 and 3720 mA g-1, respectively. Moreover, most of the prepared composite products showed high rate capability with great reversibility up to more than 90% after testing at a high current density of 3720 mA g-1. The great electrochemical performance of the MnO2/NBGC nanocomposite electrode can be attributed to the synergistic impact of the hierarchical architecture of the MnO2 nanocrystals deposited on porous carbon and the capacitive effect of the N-containing defects within the carbon material. The nanostructure of the MnO2 particles deposited on porous carbon limits its large volume change during cycling and promotes good adhesion of MnO2 nanoparticles with the substrate. Meanwhile, the capacitive effect of the exposed N-functional groups enables fast ionic conduction and reduces interfacial resistance at the electrode interface.

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Wood-Derived Carbon Fibers Embedded with SnO x Nanoparticles as Anode Material for Lithium-Ion Batteries.

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Wood-Derived Carbon Fibers Embedded with SnO <i><sub>x</sub></i> Nanoparticles as Anode Material for Lithium-Ion Batteries.

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