Atmospheric Pressure Microwave Plasma Jet for Organic Thin Film Deposition

dc.contributor.authorNarimisa, Mehrnoushcs
dc.contributor.authorKrčma, Františekcs
dc.contributor.authorOnyshchenko, Yuliiacs
dc.contributor.authorKozáková, Zdenkacs
dc.contributor.authorMorent, Rinocs
dc.contributor.authorDe Geyter, Nathaliecs
dc.coverage.issue2cs
dc.coverage.volume12cs
dc.date.issued2020-02-06cs
dc.description.abstractIn this work, the potential of a microwave (MW)induced atmospheric pressure plasma jet (APPJ) in film deposition of styrene and methyl methacrylate (MMA) precursors is investigated. Plasma properties during the deposition and resultant coating characteristics are studied. Optical emission spectroscopy (OES) results indicate a higher degree of monomer dissociation in the APPJ with increasing power and a carrier gas flow rate of up to 250 standard cubic centimeters per minute (sccm). Computational fluid dynamic (CFD) simulations demonstrate nonuniform monomer distribution near the substrate and the dependency of the deposition area on the monomercontaining gas flow rate. A nonhomogeneous surface morphology and topography of the deposited coatings is also observed using atomic force microscopy (AFM) and SEM. Coating chemical analysis and wettability are studied by XPS and water contact angle (WCA), respectively. A lower monomer flow rate was found to result in a higher C–O/C–C ratio and a higher wettability of the deposited coatings.en
dc.description.abstractIn this work, the potential of a microwave (MW)induced atmospheric pressure plasma jet (APPJ) in film deposition of styrene and methyl methacrylate (MMA) precursors is investigated. Plasma properties during the deposition and resultant coating characteristics are studied. Optical emission spectroscopy (OES) results indicate a higher degree of monomer dissociation in the APPJ with increasing power and a carrier gas flow rate of up to 250 standard cubic centimeters per minute (sccm). Computational fluid dynamic (CFD) simulations demonstrate nonuniform monomer distribution near the substrate and the dependency of the deposition area on the monomercontaining gas flow rate. A nonhomogeneous surface morphology and topography of the deposited coatings is also observed using atomic force microscopy (AFM) and SEM. Coating chemical analysis and wettability are studied by XPS and water contact angle (WCA), respectively. A lower monomer flow rate was found to result in a higher C–O/C–C ratio and a higher wettability of the deposited coatings.en
dc.formattextcs
dc.format.extent1-23cs
dc.format.mimetypeapplication/pdfcs
dc.identifier.citationPolymers. 2020, vol. 12, issue 2, p. 1-23.en
dc.identifier.doi10.3390/polym12020354cs
dc.identifier.issn2073-4360cs
dc.identifier.orcid0000-0003-4418-3323cs
dc.identifier.orcid0000-0003-3877-6587cs
dc.identifier.other165976cs
dc.identifier.researcheridAAM-2014-2021cs
dc.identifier.scopus35810645600cs
dc.identifier.urihttp://hdl.handle.net/11012/195653
dc.language.isoencs
dc.publisherMDPIcs
dc.relation.ispartofPolymerscs
dc.relation.urihttps://www.mdpi.com/2073-4360/12/2/354cs
dc.rightsCreative Commons Attribution 4.0 Internationalcs
dc.rights.accessopenAccesscs
dc.rights.sherpahttp://www.sherpa.ac.uk/romeo/issn/2073-4360/cs
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/cs
dc.subjectatmospheric pressure plasma jet (APPJ)en
dc.subjectmicrowave (MW) dischargeen
dc.subjectthin film depositionen
dc.subjectoptical emission spectroscopy (OES)en
dc.subjectComsol MultiPhysicsen
dc.subjectmethyl methacrylate (MMA)en
dc.subjectstyreneen
dc.subjectatmospheric pressure plasma jet (APPJ)
dc.subjectmicrowave (MW) discharge
dc.subjectthin film deposition
dc.subjectoptical emission spectroscopy (OES)
dc.subjectComsol MultiPhysics
dc.subjectmethyl methacrylate (MMA)
dc.subjectstyrene
dc.titleAtmospheric Pressure Microwave Plasma Jet for Organic Thin Film Depositionen
dc.title.alternativeAtmospheric Pressure Microwave Plasma Jet for Organic Thin Film Depositionen
dc.type.driverarticleen
dc.type.statusPeer-revieweden
dc.type.versionpublishedVersionen
sync.item.dbidVAV-165976en
sync.item.dbtypeVAVen
sync.item.insts2025.10.14 14:07:56en
sync.item.modts2025.10.14 10:40:18en
thesis.grantorVysoké učení technické v Brně. Fakulta chemická. Ústav fyzikální a spotřební chemiecs

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