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Improving the performance of Li-ion battery carbon anodes by in-situ immobilization of SiOx nanoparticles

[Display omitted] •C/SiOx nanocomposite was synthesized from 3-aminophenol and TEOS.•SiO2 formation and 3-aminophenol polymerization took place in microwave.•Effectiveness of three types of heating protocols for SiO2 reduction was evaluated.•It took 15 wt% of SiOx to improve the lithium ion battery...

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Bibliographic Details
Published in:Materials research bulletin 2019-04, Vol.112, p.16-21
Main Authors: Izawa, Takafumi, Arif, Aditya F., Taniguchi, Shuto, Kamikubo, Kazuki, Iwasaki, Hideharu, Ogi, Takashi
Format: Article
Language:English
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Summary:[Display omitted] •C/SiOx nanocomposite was synthesized from 3-aminophenol and TEOS.•SiO2 formation and 3-aminophenol polymerization took place in microwave.•Effectiveness of three types of heating protocols for SiO2 reduction was evaluated.•It took 15 wt% of SiOx to improve the lithium ion battery performance by 30%. A 30% improvement of the capacity of a lithium ion battery was demonstrated by introducing a C/SiOx nanocomposite electrode having a SiOx nanoparticle loading of 15 wt.%. The nanocomposite was tailored from tetraethyl orthosilicate (TEOS) and 3-aminophenol which simultaneously underwent hydrolysis-condensation and polymerization, respectively, to produce a C/SiO2 intermediate when subjected to microwave irradiation. SiO2 was present as nanoparticles on the carbon surface, which allowed for facile reduction. Under a mild reducing agent, concurrent carbonization of the 3-aminophenol polymer and the reduction of SiO2 nanoparticles were performed. The value of x in the synthesized C/SiOx was 1.24 according to the binding energy from the Si 2p x-ray photoelectron spectroscopy spectrum. The synthesized C/SiOx nanocomposite delivered a reversible capacity of 383 mA h/g as a lithium battery anode—a 30% improvement on the carbon-only electrode. Charge-discharge cycling shows 84% capacity retention after 100 cycles.
ISSN:0025-5408
1873-4227
DOI:10.1016/j.materresbull.2018.11.044