Patterning of supported gold monolayers via chemical lift-off lithography

dc.citation.firstpage2648en_US
dc.citation.journalTitleBeilstein Journal of Nanotechnologyen_US
dc.citation.lastpage2661en_US
dc.citation.volumeNumber8en_US
dc.contributor.authorSlaughter, Liane S.en_US
dc.contributor.authorCheung, Kevin M.en_US
dc.contributor.authorKaappa, Samien_US
dc.contributor.authorCao, Huan H.en_US
dc.contributor.authorYang, Qingen_US
dc.contributor.authorYoung, Thomas D.en_US
dc.contributor.authorSerino, Andrew C.en_US
dc.contributor.authorMalola, Samien_US
dc.contributor.authorOlson, Jana M.en_US
dc.contributor.authorLink, Stephanen_US
dc.contributor.authorHäkkinen, Hannuen_US
dc.contributor.authorAndrews, Anne M.en_US
dc.contributor.authorWeiss, Paul S.en_US
dc.date.accessioned2017-12-18T18:19:41Zen_US
dc.date.available2017-12-18T18:19:41Zen_US
dc.date.issued2017en_US
dc.description.abstractThe supported monolayer of Au that accompanies alkanethiolate molecules removed by polymer stamps during chemical lift-off lithography is a scarcely studied hybrid material. We show that these Au–alkanethiolate layers on poly(dimethylsiloxane) (PDMS) are transparent, functional, hybrid interfaces that can be patterned over nanometer, micrometer, and millimeter length scales. Unlike other ultrathin Au films and nanoparticles, lifted-off Au–alkanethiolate thin films lack a measurable optical signature. We therefore devised fabrication, characterization, and simulation strategies by which to interrogate the nanoscale structure, chemical functionality, stoichiometry, and spectral signature of the supported Au–thiolate layers. The patterning of these layers laterally encodes their functionality, as demonstrated by a fluorescence-based approach that relies on dye-labeled complementary DNA hybridization. Supported thin Au films can be patterned via features on PDMS stamps (controlled contact), using patterned Au substrates prior to lift-off (e.g., selective wet etching), or by patterning alkanethiols on Au substrates to be reactive in selected regions but not others (controlled reactivity). In all cases, the regions containing Au–alkanethiolate layers have a sub-nanometer apparent height, which was found to be consistent with molecular dynamics simulations that predicted the removal of no more than 1.5 Au atoms per thiol, thus presenting a monolayer-like structure.en_US
dc.identifier.citationSlaughter, Liane S., Cheung, Kevin M., Kaappa, Sami, et al.. "Patterning of supported gold monolayers via chemical lift-off lithography." <i>Beilstein Journal of Nanotechnology,</i> 8, (2017) Beilstein: 2648-2661. https://doi.org/10.3762/bjnano.8.265.en_US
dc.identifier.digitalPatterning-supported-gold-monolayersen_US
dc.identifier.doihttps://doi.org/10.3762/bjnano.8.265en_US
dc.identifier.urihttps://hdl.handle.net/1911/98886en_US
dc.language.isoengen_US
dc.publisherBeilsteinen_US
dc.rightsThis is an Open Access article under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.en_US
dc.rights.urihttp://creativecommons.org/licenses/by/4.0en_US
dc.subject.keywordchemical patterningen_US
dc.subject.keywordhybrid materialen_US
dc.subject.keywordmonolayeren_US
dc.subject.keywordsoft lithographyen_US
dc.subject.keywordtwo-dimensional materialen_US
dc.titlePatterning of supported gold monolayers via chemical lift-off lithographyen_US
dc.typeJournal articleen_US
dc.type.dcmiTexten_US
dc.type.publicationpublisher versionen_US
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