Carbothermal conversion of boric acid into boron-oxy-carbide nanostructures for high-power supercapacitors
In this study, we report a facile carbothermal method for the preparation of boron-oxy-carbide (BOC) nanostructures and explore their properties towards electrochemical energy storage devices. The formation of lamella-like BOC ceramic nanostructures in which boron suboxides are confined in the carbo...
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Veröffentlicht in: | Journal of materials chemistry. A, Materials for energy and sustainability Materials for energy and sustainability, 2021-01, Vol.9 (2), p.915-921 |
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Sprache: | eng |
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Zusammenfassung: | In this study, we report a facile carbothermal method for the preparation of boron-oxy-carbide (BOC) nanostructures and explore their properties towards electrochemical energy storage devices. The formation of lamella-like BOC ceramic nanostructures in which boron suboxides are confined in the carbon matrix was confirmed using high-resolution transmission electron micrographs and X-ray photoelectron spectral analyses. A symmetric supercapacitor (SSC) fabricated using BOC electrodes demonstrated their stable operation over a wide voltage window of 2.0 V in the TEABF
4
electrolyte. The BOC SSC possesses high capacitance (7.26 mF cm
−2
), high energy density (14.53 mJ cm
−2
) with better rate capability, and a long-life cycle. Further, BOC SSC possesses a low equivalent series resistance (1.44 Ω), which in turn leads to the achievement of a high maximal power density (373 mW cm
−2
) that makes it a better alternative to the reported silicon- and carbon-based supercapacitors. In addition, we have also demonstrated a self-charging power system
via
extrinsically integrating BOC SSC with a thermoelectric power station that further highlights their applications in next-generation energy storage and management sectors.
In this study, we report a facile carbothermal method for the preparation of boron-oxy-carbide (BOC) nanostructures and explore their properties towards electrochemical energy storage devices. |
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ISSN: | 2050-7488 2050-7496 |
DOI: | 10.1039/d0ta09154e |