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dc.contributor.authorGriffin, John
dc.contributor.authorForse, Alexander
dc.contributor.authorTsai, Wan-Yu
dc.contributor.authorTaberna, Pierre-Louis
dc.contributor.authorSimon, Patrice
dc.contributor.authorGrey, Clare
dc.date.accessioned2015-06-24T13:41:32Z
dc.date.available2015-06-24T13:41:32Z
dc.date.issued2015-08
dc.identifier.citationNature Materials 14, 812–819 (2015). doi:10.1038/nmat4318
dc.identifier.issn1476-1122
dc.identifier.urihttps://www.repository.cam.ac.uk/handle/1810/248674
dc.description.abstractSupercapacitors store charge through the electrosorption of ions on microporous electrodes. Despite major efforts to understand this phenomenon, a molecular-level picture of the electrical double layer in working devices is still lacking as few techniques can selectively observe the ionic species at the electrode/electrolyte interface. Here, we use in situ NMR to directly quantify the populations of anionic and cationic species within a working microporous carbon supercapacitor electrode. Our results show that charge storage mechanisms are different for positively and negatively polarized electrodes for the electrolyte tetraethylphosphonium tetrafluoroborate in acetonitrile; for positive polarization charging proceeds by exchange of the cations for anions, whereas for negative polarization, cation adsorption dominates. In situ electrochemical quartz crystal microbalance measurements support the NMR results and indicate that adsorbed ions are only partially solvated. These results provide new molecular-level insight, with the methodology offering exciting possibilities for the study of pore/ion size, desolvation and other effects on charge storage in supercapacitors.
dc.description.sponsorshipA.C.F., J.M.G. and C.P.G. acknowledge the Sims Scholarship (A.C.F.), EPSRC (through the Supergen consortium for J.M.G.) and the EU ERC (through an Advanced Fellowship to C.P.G.) for financial support. P.S. and W.-Y.T. acknowledge support from the European Research Council (ERC, Advanced Grant, ERC-2011-AdG, Project 291543–IONACES). P.S. also acknowledges financial support from the Chair ‘Embedded Multi-Functional Nanomaterials’ from the Airbus Group Foundation. A.C.F. and J.M.G. thank the NanoDTC Cambridge for travel funding.
dc.languageEnglish
dc.language.isoen
dc.publisherSpringer Science and Business Media LLC
dc.titleIn situ NMR and electrochemical quartz crystal microbalance techniques reveal the structure of the electrical double layer in supercapacitors.
dc.typeArticle
dc.description.versionThis is the author accepted manuscript. The final version is available from NPG at http://www.nature.com/nmat/journal/vaop/ncurrent/full/nmat4318.html#abstract.  
prism.endingPage819
prism.publicationDate2015
prism.publicationNameNat Mater
prism.startingPage812
prism.volume14
dc.rioxxterms.funderEPSRC
dcterms.dateAccepted2015-04-23
rioxxterms.versionofrecord10.1038/nmat4318
rioxxterms.licenseref.urihttp://www.rioxx.net/licenses/all-rights-reserved
rioxxterms.licenseref.startdate2015-06-22
dc.contributor.orcidForse, Alexander [0000-0001-9592-9821]
dc.contributor.orcidGrey, Clare [0000-0001-5572-192X]
dc.identifier.eissn1476-4660
rioxxterms.typeJournal Article/Review
pubs.funder-project-idEngineering and Physical Sciences Research Council (EP/L019469/1)
pubs.funder-project-idEngineering and Physical Sciences Research Council (EP/K002252/1)
cam.issuedOnline2015-06-22
rioxxterms.freetoread.startdate2015-12-22


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