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Enriched supercapacitive performance of electrochemically tailored β-Co(OH)2/CoOOH nanodiscs from sacrificial Co3(PO4)2·4H2O microbelts
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Title
Enriched supercapacitive performance of electrochemically tailored β-Co(OH)2/CoOOH nanodiscs from sacrificial Co3(PO4)2·4H2O microbelts
Issued Date
2024-05
Citation
Koppisetti, Heramba V. S. R. M. (2024-05). Enriched supercapacitive performance of electrochemically tailored β-Co(OH)2/CoOOH nanodiscs from sacrificial Co3(PO4)2·4H2O microbelts. Journal of Energy Storage, 86. doi: 10.1016/j.est.2024.111178
Type
Article
Keywords
CO-3(OH)(2)(HPO4)(2)ELECTROCATALYSTCOMPOSITEEFFICIENTCATHODEELECTRODE MATERIALCOBALT HYDROXIDEHYBRID
ISSN
2352-152X
Abstract
Electrochemically induced structural reconstruction process of metal precursors into their corresponding metal hydroxides/(oxy)hydroxides is developed as an ingenious strategy towards preparing efficient electrode material. However, the influence of electrochemical activation on the charge storage ability of electrode material is barely explored. Herein, we have utilized a synthetic strategy (solvothermal reaction in water:ethanol mixture) to prepare Co3(PO4)2·4H2O microbelts and subsequently applied the electrochemical bulk reconstruction process in 1 M KOH electrolyte. A thorough physical and electrochemical characterization unveil that the electrode material is converted into redox active site rich β-Co(OH)2/CoOOH nanodiscs via etching of lattice anionic PO43− moieties. The material possesses a specific capacitance of 386 F g−1at a current density of 0.25 A g−1. Additionally, a hybrid device constructed with β-Co(OH)2/CoOOH nanodiscs and activated charcoal (AC) as positive and negative electrodes has achieved a high energy density of 13.33 Wh Kg−1at a power density of 400 W kg−1. Further, the device displayed a good capacitance retention of 93 % (columbic efficiency ~98 %) up to 10,000 cycles. The improved charge storage of reconstructed material with abundant redox active sites could be attributed to the facile diffusion of electrolyte ions into the bulk of the material. © 2024 Elsevier Ltd
URI
http://hdl.handle.net/20.500.11750/56996
DOI
10.1016/j.est.2024.111178
Publisher
Elsevier
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