Please use this identifier to cite or link to this item: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/2633
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dc.contributor.authorOndarcuhu, Thierryen_US
dc.contributor.authorThomas, Vincenten_US
dc.contributor.authorNunez, Marcen_US
dc.contributor.authorDujardin, Eriken_US
dc.contributor.authorRAHMAN, ATIKURen_US
dc.contributor.authorBlack, Charles T.en_US
dc.contributor.authorChecco, Antonioen_US
dc.date.accessioned2019-04-29T09:21:49Z
dc.date.available2019-04-29T09:21:49Z
dc.date.issued2016-04en_US
dc.identifier.citationScientific Reports, 6, 24237.en_US
dc.identifier.issn2045-2322en_US
dc.identifier.urihttp://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/2633-
dc.identifier.urihttps://doi.org/10.1038/srep24237en_US
dc.description.abstractThe dependence of the wettability of graphene on the nature of the underlying substrate remains only partially understood. Here, we systematically investigate the role of liquid-substrate interactions on the wettability of graphene by varying the area fraction of suspended graphene from 0 to 95% by means of nanotextured substrates. We find that completely suspended graphene exhibits the highest water contact angle (85° ± 5°) compared to partially suspended or supported graphene, regardless of the hydrophobicity (hydrophilicity) of the substrate. Further, 80% of the long-range water-substrate interactions are screened by the graphene monolayer, the wettability of which is primarily determined by short-range graphene-liquid interactions. By its well-defined chemical and geometrical properties, supported graphene therefore provides a model system to elucidate the relative contribution of short and long range interactions to the macroscopic contact angle.en_US
dc.language.isoenen_US
dc.publisherNature Publishing Groupen_US
dc.subjectWettabilityen_US
dc.subjectPartially suspended grapheneen_US
dc.subjectFabricationen_US
dc.subjectGraphene monolayers transferreden_US
dc.subjectPolymer contaminationen_US
dc.subjectHydrophobic substratesen_US
dc.subject2016en_US
dc.titleWettability of partially suspended grapheneen_US
dc.typeArticleen_US
dc.contributor.departmentDept. of Physicsen_US
dc.identifier.sourcetitleScientific Reportsen_US
dc.publication.originofpublisherForeignen_US
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