Please use this identifier to cite or link to this item: https://doi.org/10.1021/acs.jpcc.9b01060
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dc.titlePH Dependence of Ultrafast Charge Dynamics in Graphene Oxide Dispersions
dc.contributor.authorKime, G
dc.contributor.authorZhou, KG
dc.contributor.authorHardman, SJO
dc.contributor.authorNair, RR
dc.contributor.authorNovoselov, KS
dc.contributor.authorAndreeva, DV
dc.contributor.authorBinks, DJ
dc.date.accessioned2023-06-14T05:29:13Z
dc.date.available2023-06-14T05:29:13Z
dc.date.issued2019-04-25
dc.identifier.citationKime, G, Zhou, KG, Hardman, SJO, Nair, RR, Novoselov, KS, Andreeva, DV, Binks, DJ (2019-04-25). PH Dependence of Ultrafast Charge Dynamics in Graphene Oxide Dispersions. Journal of Physical Chemistry C 123 (16) : 10677-10681. ScholarBank@NUS Repository. https://doi.org/10.1021/acs.jpcc.9b01060
dc.identifier.issn1932-7447
dc.identifier.issn1932-7455
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/241951
dc.description.abstractThe pH dependence of emission from graphene oxide is believed to be due to the protonation of surface functional groups. In this study, we use transient absorption spectroscopy to study the sub-picosecond charge dynamics in graphene oxide over a range of pH values, observing dynamics consistent with an excited-state protonation step for pH < 9.3. The timescale of this process is ?1.5 ps, and a corresponding change in recombination dynamics follows. A broad photo-induced absorption peak centered at 530 nm associated with excited-state protonation is also observed.
dc.publisherAmerican Chemical Society (ACS)
dc.sourceElements
dc.subjectcond-mat.mtrl-sci
dc.subjectcond-mat.mtrl-sci
dc.subjectphysics.chem-ph
dc.typeArticle
dc.date.updated2023-06-06T02:18:58Z
dc.contributor.departmentMATERIALS SCIENCE AND ENGINEERING
dc.description.doi10.1021/acs.jpcc.9b01060
dc.description.sourcetitleJournal of Physical Chemistry C
dc.description.volume123
dc.description.issue16
dc.description.page10677-10681
dc.published.statePublished
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