Please use this identifier to cite or link to this item: https://doi.org/10.1016/j.carbon.2012.11.002
DC FieldValue
dc.titleThe production of organogels using graphene oxide as the gelator for use in high-performance quasi-solid state dye-sensitized solar cells
dc.contributor.authorNeo, C.Y.
dc.contributor.authorOuyang, J.
dc.date.accessioned2014-10-07T09:54:53Z
dc.date.available2014-10-07T09:54:53Z
dc.date.issued2013-04
dc.identifier.citationNeo, C.Y., Ouyang, J. (2013-04). The production of organogels using graphene oxide as the gelator for use in high-performance quasi-solid state dye-sensitized solar cells. Carbon 54 : 48-57. ScholarBank@NUS Repository. https://doi.org/10.1016/j.carbon.2012.11.002
dc.identifier.issn00086223
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/86795
dc.description.abstractWe report the formation of organogels of 3-methoxypropionitrile (MPN) using graphene oxide (GO) as the gelator and the use of these gels as the quasi-solid state electrolyte of dye-sensitized solar cells (DSCs). GO-MPN gels are prepared by mechanically grinding or ultrasonicating GO in MPN. The GO sheets form 3-dimensional solid networks in the gels, which hold the MPN solvent. The GO loading can be as low as 2.5 wt.% for the gel formation. Gel electrolytes were prepared by dispersing I2, 1-methyl-3-propylimidazolium iodide, guanidine thiocynate and 4-tert butyl pyridine into GO-MPN gels, and these were used for DSCs. The GO sheets can be fragmented into small pieces by ultrasonication, and smaller GO sheets can lead to a higher diffusion constant of the triiodide and a higher photovoltaic efficiency for the DSCs. DSCs with a GO-MPN gel electrolyte exhibit a photovoltaic efficiency of 6.70% under AM 1.5 G illumination (100 mW cm-2), quite close to that (7.18%) of the control liquid DSCs. © 2012 Elsevier Ltd. All rights reserved.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1016/j.carbon.2012.11.002
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentMATERIALS SCIENCE AND ENGINEERING
dc.description.doi10.1016/j.carbon.2012.11.002
dc.description.sourcetitleCarbon
dc.description.volume54
dc.description.page48-57
dc.description.codenCRBNA
dc.identifier.isiut000315541500006
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