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dc.contributor.authorLi, Tingting
dc.contributor.authorYang, Shaokang
dc.contributor.authorZuo, Yunpeng
dc.contributor.authorLi, Wei
dc.contributor.authorKment, Štěpán
dc.contributor.authorChai, Yang
dc.date.accessioned2023-02-16T09:21:35Z
dc.date.available2023-02-16T09:21:35Z
dc.date.issued2022
dc.identifier.citationInorganic Chemistry Frontiers. 2022, vol. 10, issue 3, p. 1001-1010.cs
dc.identifier.issn2052-1553
dc.identifier.urihttp://hdl.handle.net/10084/149114
dc.description.abstractTo improve the intrinsic property of Ni(OH)(2) for advanced supercapacitors, structural and valence engineering are combined here to prepare porous beta-Ni(OH)(x)-SO4 (NSO) interlaminar materials. NSO has an expanded interplanar spacing and in-plane porous channels, thus offering a 3D accessible structure for the charging and discharging process. The intercalation of SO42- can retain the layer spacing of NSO through hydrogen bond during the charge transport and effectively drive electrons close to the Fermi level of NSO, which significantly enhances the stability and conductivity of the sample. The rigid interlayer space and in-plane channels enable NSO to exhibit a high specific capacity of 212.5 mA h g(-1) at 3 A g(-1). The assembled asymmetric supercapacitor device shows a high energy density of 41.2 W h kg(-1) at 796.9 W kg(-1) and maintains 86.8% capacity retention after 10 000 cycles at 4 A g(-1).cs
dc.language.isoencs
dc.publisherRoyal Society of Chemistrycs
dc.relation.ispartofseriesInorganic Chemistry Frontierscs
dc.relation.urihttps://doi.org/10.1039/d2qi01992bcs
dc.titleHydrogen bond stabilized beta-Ni(OH)(x)-SO4 interlaminar materials for highly active supercapacitorscs
dc.typearticlecs
dc.identifier.doi10.1039/d2qi01992b
dc.type.statusPeer-reviewedcs
dc.description.sourceWeb of Sciencecs
dc.description.volume10cs
dc.description.issue3cs
dc.description.lastpage1010cs
dc.description.firstpage1001cs
dc.identifier.wos000903004700001


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