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dc.contributor.authorVidhya, M. Sangeetha
dc.contributor.authorYuvakkumar, R.
dc.contributor.authorRavi, G.
dc.contributor.authorSaravanakumar, B.
dc.contributor.authorVelauthapillai, Dhayalan
dc.date.accessioned2023-05-05T12:28:29Z
dc.date.available2023-05-05T12:28:29Z
dc.date.created2022-02-27T00:34:05Z
dc.date.issued2021
dc.identifier.citationNanoscale Advances. 2021, 3 (14), 4207-4215.en_US
dc.identifier.issn2516-0230
dc.identifier.urihttps://hdl.handle.net/11250/3066480
dc.description.abstractThe polyhedron-structured NiSe2@MoSe2 (NMS) were magnificently produced through hydrothermal method, which makes the active electrode very effective in accessing the redox active sites in the charge/discharge process in supercapacitor applications. Systematic studies of the structural and morphological features of the unique polyhedron NMS were performed. Laser Raman spectra reported the vibrational and rotational modes of NMS. NMS exhibited a maximum 1000 F g−1 (138.8 mA h g−1) specific capacitance at 1 A g−1 and attained a capacity retention of 77.67% for 5000 stable cycles at 10 A g−1 using 1 M KOH as an electrolyte. The well assembled asymmetric supercapacitor NMS hydrolyzed for 18 h//AC demonstrated an outstanding electrochemical performance with an improved 305 F g−1 specific capacitance attained at 1 A g−1 with a good cycle life of 87.35% and a capacity retention of over 5000 cycles. Herein, the combined contribution of both the Ni and Mo ions offers a richer redox chemistry, which is beneficial to a higher electrochemical activity. The experimental results indicate that the NMS electrode could be used as a high-performance electrode.en_US
dc.language.isoengen_US
dc.publisherRoyal Society of Chemistryen_US
dc.rightsNavngivelse 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/deed.no*
dc.titleAsymmetric polyhedron structured NiSe2@MoSe2 device for use as a supercapacitoren_US
dc.typePeer revieweden_US
dc.typeJournal articleen_US
dc.description.versionpublishedVersionen_US
dc.rights.holder© 2021 The Author(s)en_US
dc.source.pagenumber4207-4215en_US
dc.source.volume3en_US
dc.source.journalNanoscale Advancesen_US
dc.source.issue14en_US
dc.identifier.doi10.1039/d0na01047b
dc.identifier.cristin2005788
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1


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