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dc.contributor.authorChen, X.
dc.contributor.authorLuais, E.
dc.contributor.authorDarwish, Nadim
dc.contributor.authorCiampi, S.
dc.contributor.authorThordarson, P.
dc.contributor.authorGooding, J.
dc.date.accessioned2017-01-30T11:26:46Z
dc.date.available2017-01-30T11:26:46Z
dc.date.created2016-05-19T19:30:18Z
dc.date.issued2012
dc.identifier.citationChen, X. and Luais, E. and Darwish, N. and Ciampi, S. and Thordarson, P. and Gooding, J. 2012. Studies on the effect of solvents on self-assembled monolayers formed from organophosphonic acids on indium tin oxide. Langmuir. 28 (25): pp. 9487-9495.
dc.identifier.urihttp://hdl.handle.net/20.500.11937/11757
dc.identifier.doi10.1021/la3010129
dc.description.abstract

The preparation of self-assembled monolayers (SAMs) of organophosphonic acids on indium tin oxide (ITO) surfaces from different solvents (triethylamine, ethyl ether, tetrahydofuran (THF), pyridine, acetone, methanol, acetonitrile, dimethyl sulfoxide (DMSO), or water) has been performed with some significant differences observed. Cyclic voltammetry (CV), X-ray photoelectron spectroscopy (XPS), scanning tunneling microscopy (STM), and contact angle measurement demonstrated that the quality of SAMs depends critically on the choice of solvents. Higher density, more stable monolayers were formed from solvents with low dielectric constants and weak interactions with the ITO. It was concluded low dielectric solvents that were inert to the ITO gave monolayers that were more stable with a higher density of surface bound molecules because higher dielectric constant solvents and solvents that coordinate with the surface disrupted SAM formation.

dc.publisherAmerican Chemical Society
dc.titleStudies on the effect of solvents on self-assembled monolayers formed from organophosphonic acids on indium tin oxide
dc.typeJournal Article
dcterms.source.volume28
dcterms.source.number25
dcterms.source.startPage9487
dcterms.source.endPage9495
dcterms.source.issn0743-7463
dcterms.source.titleLangmuir
curtin.departmentNanochemistry Research Institute
curtin.accessStatusFulltext not available


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