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dc.contributor.authorKinnunen, Sami
dc.contributor.authorLahtinen, Manu
dc.contributor.authorArstila, Kai
dc.contributor.authorSajavaara, Timo
dc.date.accessioned2021-05-18T11:25:52Z
dc.date.available2021-05-18T11:25:52Z
dc.date.issued2021
dc.identifier.citationKinnunen, S., Lahtinen, M., Arstila, K., & Sajavaara, T. (2021). Hydrogen and Deuterium Incorporation in ZnO Films Grown by Atomic Layer Deposition. <i>Coatings</i>, <i>11</i>(5), Article 542. <a href="https://doi.org/10.3390/coatings11050542" target="_blank">https://doi.org/10.3390/coatings11050542</a>
dc.identifier.otherCONVID_83401498
dc.identifier.urihttps://jyx.jyu.fi/handle/123456789/75735
dc.description.abstractZinc oxide (ZnO) thin films were grown by atomic layer deposition using diethylzinc (DEZ) and water. In addition to depositions with normal water, heavy water (2H2O) was used in order to study the reaction mechanisms and the hydrogen incorporation at different deposition temperatures from 30 to 200 °C. The total hydrogen concentration in the films was found to increase as the deposition temperature decreased. When the deposition temperature decreased close to room temperature, the main source of impurity in hydrogen changed from 1H to 2H. A sufficiently long purging time changed the main hydrogen isotope incorporated in the film back to 1H. A multiple short pulse scheme was used to study the transient steric hindrance. In addition, the effect of the storage of the samples in ambient conditions was studied. During the storage, the deuterium concentration decreased while the hydrogen concentration increased an equal amount, indicating that there was an isotope exchange reaction with ambient H2 and/or H2O.en
dc.format.mimetypeapplication/pdf
dc.language.isoeng
dc.publisherMDPI AG
dc.relation.ispartofseriesCoatings
dc.rightsCC BY 4.0
dc.subject.otherZnO
dc.subject.otherALD
dc.subject.otherheavy water
dc.subject.otherdiethylzinc
dc.subject.otherToF-ERDA
dc.titleHydrogen and Deuterium Incorporation in ZnO Films Grown by Atomic Layer Deposition
dc.typearticle
dc.identifier.urnURN:NBN:fi:jyu-202105183001
dc.contributor.laitosKemian laitosfi
dc.contributor.laitosFysiikan laitosfi
dc.contributor.laitosDepartment of Chemistryen
dc.contributor.laitosDepartment of Physicsen
dc.contributor.oppiaineEpäorgaaninen ja analyyttinen kemiafi
dc.contributor.oppiaineEpäorgaaninen kemiafi
dc.contributor.oppiaineYdin- ja kiihdytinfysiikan huippuyksikköfi
dc.contributor.oppiaineFysiikkafi
dc.contributor.oppiaineInorganic and Analytical Chemistryen
dc.contributor.oppiaineInorganic Chemistryen
dc.contributor.oppiaineCentre of Excellence in Nuclear and Accelerator Based Physicsen
dc.contributor.oppiainePhysicsen
dc.type.urihttp://purl.org/eprint/type/JournalArticle
dc.type.coarhttp://purl.org/coar/resource_type/c_2df8fbb1
dc.description.reviewstatuspeerReviewed
dc.relation.issn2079-6412
dc.relation.numberinseries5
dc.relation.volume11
dc.type.versionpublishedVersion
dc.rights.copyright© 2021 by the authors. Licensee MDPI, Basel, Switzerland.
dc.rights.accesslevelopenAccessfi
dc.subject.ysovety
dc.subject.ysoatomikerroskasvatus
dc.subject.ysosinkkioksidi
dc.subject.ysoohutkalvot
dc.format.contentfulltext
jyx.subject.urihttp://www.yso.fi/onto/yso/p16151
jyx.subject.urihttp://www.yso.fi/onto/yso/p27468
jyx.subject.urihttp://www.yso.fi/onto/yso/p27694
jyx.subject.urihttp://www.yso.fi/onto/yso/p16644
dc.rights.urlhttps://creativecommons.org/licenses/by/4.0/
dc.relation.doi10.3390/coatings11050542
jyx.fundinginformationThis research received no external funding.
dc.type.okmA1


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