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dc.date.accessioned2024-03-22T17:55:13Z
dc.date.available2024-03-22T17:55:13Z
dc.date.created2023-06-19T10:55:14Z
dc.date.issued2023
dc.identifier.citationFrodason, Ymir Kalmann Krzyzaniak, Patryk Piotr Vines, Lasse Varley, Joel Basile Van De Walle, Chris G. Johansen, Klaus Magnus H . Diffusion of Sn donors in β-Ga2O3. APL Materials. 2023, 11(4)
dc.identifier.urihttp://hdl.handle.net/10852/109983
dc.description.abstractDiffusion of the n-type dopant Sn in β-Ga2O3 is studied using secondary-ion mass spectrometry combined with hybrid functional calculations. The diffusion of Sn from a Sn-doped bulk substrate with surface orientation (001) into an epitaxial layer is observed after heat treatments in the temperature range of 1050–1250 °C. Calculated formation energies of Sn-related and intrinsic defects show that the migration of Sn is mediated by Ga vacancies (VGa) through the formation and dissociation of intermittent mobile VGaSnGa complexes. The evolution of the Sn concentration vs depth profiles after heat treatments can be well described by a reaction–diffusion model. Using model parameters guided by the hybrid functional calculations, we extract a VGaSnGa complex migration barrier of 3.0 ± 0.4 eV with a diffusion coefficient of 2 × 10−1 cm2/s. The extracted migration barrier is consistent with our theoretical predictions using the nudged elastic band method, which shows migration barriers of 3.42, 3.15, and 3.37 eV for the [100], [010], and [001] directions, respectively.
dc.languageEN
dc.publisherAIP (American Institute of Physics)
dc.rightsAttribution 4.0 International
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.titleDiffusion of Sn donors in β-Ga2O3
dc.title.alternativeENEngelskEnglishDiffusion of Sn donors in β-Ga2O3
dc.typeJournal article
dc.creator.authorFrodason, Ymir Kalmann
dc.creator.authorKrzyzaniak, Patryk Piotr
dc.creator.authorVines, Lasse
dc.creator.authorVarley, Joel Basile
dc.creator.authorVan De Walle, Chris G.
dc.creator.authorJohansen, Klaus Magnus H
cristin.unitcode185,15,17,20
cristin.unitnameSenter for Materialvitenskap og Nanoteknologi fysikk
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1
dc.identifier.cristin2155726
dc.identifier.bibliographiccitationinfo:ofi/fmt:kev:mtx:ctx&ctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=APL Materials&rft.volume=11&rft.spage=&rft.date=2023
dc.identifier.jtitleAPL Materials
dc.identifier.volume11
dc.identifier.issue4
dc.identifier.doihttps://doi.org/10.1063/5.0142671
dc.type.documentTidsskriftartikkel
dc.type.peerreviewedPeer reviewed
dc.source.issn2166-532X
dc.type.versionPublishedVersion
cristin.articleid041121
dc.relation.projectNFR/314017
dc.relation.projectSIGMA2/NN9136K
dc.relation.projectNFR/295864


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