Please use this identifier to cite or link to this item: https://doi.org/10.1039/c3ta13938g
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dc.titleThe role of ions and reaction sites for electrochemical reversible charge cycling in mesoporous nickel hydroxides
dc.contributor.authorLiu, J.
dc.contributor.authorRen, Y.
dc.contributor.authorDasgupta, B.
dc.contributor.authorTanoto, H.
dc.contributor.authorSeng, H.L.
dc.contributor.authorChim, W.K.
dc.contributor.authorLi, S.F.Y.
dc.contributor.authorChiam, S.Y.
dc.date.accessioned2014-06-17T03:08:27Z
dc.date.available2014-06-17T03:08:27Z
dc.date.issued2013-12-21
dc.identifier.citationLiu, J., Ren, Y., Dasgupta, B., Tanoto, H., Seng, H.L., Chim, W.K., Li, S.F.Y., Chiam, S.Y. (2013-12-21). The role of ions and reaction sites for electrochemical reversible charge cycling in mesoporous nickel hydroxides. Journal of Materials Chemistry A 1 (47) : 15095-15101. ScholarBank@NUS Repository. https://doi.org/10.1039/c3ta13938g
dc.identifier.issn20507488
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/57635
dc.description.abstractLayered nickel hydroxide thin films with mesoporous structure were prepared on ITO substrates by a facile chemical bath deposition method. The electrochemical properties of the nickel hydroxide/oxyhydroxide films were investigated in both potassium hydroxide and lithium perchlorate in propylene carbonate electrolytes. We show that the high reversible charge cycling capability of the material is enabled by the redox reaction involving hydroxyl ions, especially in the oxidative cycle. Li ion reversible charge cycling requires available reaction or adsorption sites that can be provided by sub-stoichiometry or defective films. Raising the defect concentration, the cyclic reversibility is shown to increase by ∼5 times. The effects of intercalated water in the interlayers are also discussed. We show that the presence of water in the interlayers can lead to a passivating reaction during the charge cycling and also cause optical efficiency losses through unwanted charge trapping. © 2013 The Royal Society of Chemistry.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1039/c3ta13938g
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentELECTRICAL & COMPUTER ENGINEERING
dc.contributor.departmentCHEMISTRY
dc.description.doi10.1039/c3ta13938g
dc.description.sourcetitleJournal of Materials Chemistry A
dc.description.volume1
dc.description.issue47
dc.description.page15095-15101
dc.description.codenJMCAE
dc.identifier.isiut000326984500037
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