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dc.contributor.authorZhou, Haitao
dc.contributor.authorChen, De
dc.date.accessioned2020-07-07T08:28:13Z
dc.date.available2020-07-07T08:28:13Z
dc.date.created2020-01-19T23:36:24Z
dc.date.issued2019
dc.identifier.citationJournal of Materials Chemistry A. 2019, 7 (17), 9708-9715.en_US
dc.identifier.issn2050-7488
dc.identifier.urihttps://hdl.handle.net/11250/2660909
dc.description.abstractZn-ion hybrid supercapacitors have been proposed as a promising energy storage candidate compared to Li-ion hybrid technology due to the highly abundant Zn resources and their low cost. However, simultaneously achieving high volumetric energy density and high power density of the hybrid supercapacitors remains a challenge. Herein, we report new Zn-ion hybrid supercapacitors using functionalized carbon nanosponges as cathode materials and Zn(CF3SO3)2 in both an ionic liquid (IL) and acetonitrile (AN) as the electrolyte. We revealed both experimentally and theoretically a remarkable increase of the performance by controlling macro/mesoporous structure and surface chemistry of the carbon sponge, through the pseudocapacitance induced by proton transfer. The estimated volumetric energy density of the fully packed cell with an IL (2.4 V) is as high as 54.3 W h L−1. An ultrahigh power density of 17.7 kW L−1 with 18.8 W h L−1 was achieved by replacing the IL with AN. The full charge/discharge of the SCs with AN took only 11 seconds. More importantly, a remarkably stable performance was achieved with no capacitance fading for over 60 000 cycles. The results enlighten and promote the design and preparation of functionalized carbon positive electrodes to develop high-performance dual-ion energy storage devices.en_US
dc.language.isoengen_US
dc.publisherThe Royal Society of Chemistryen_US
dc.titleBoosting the electrochemical performance through proton transfer for the Zn-ion hybrid supercapacitor with both ionic liquid and organic electrolytesen_US
dc.typePeer revieweden_US
dc.typeJournal articleen_US
dc.description.versionpublishedVersionen_US
dc.source.pagenumber9708-9715en_US
dc.source.volume7en_US
dc.source.journalJournal of Materials Chemistry Aen_US
dc.source.issue17en_US
dc.identifier.doi10.1039/c9ta01256g
dc.identifier.cristin1717518
dc.description.localcodeThis article will not be available due to copyright restrictions (c) 2019 by The Royal Society of Chemistryen_US
cristin.unitcode194,66,30,0
cristin.unitnameInstitutt for kjemisk prosessteknologi
cristin.ispublishedtrue
cristin.fulltextpostprint
cristin.qualitycode1


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