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dc.contributor.authorWafula, Henry
dc.contributor.authorRobinson, Musembi
dc.contributor.authorJuma, Albert
dc.contributor.authorSakwa, Thomas
dc.contributor.authore Kitui, Manass
dc.contributor.authorAraoz, Rodrigo
dc.contributor.authorFischer, Christian-H.
dc.date.accessioned2023-07-06T11:22:47Z
dc.date.available2023-07-06T11:22:47Z
dc.date.issued2015-02-15
dc.identifier.urihttps://doi.org/10.3390/coatings5010054
dc.identifier.urihttps://www.mdpi.com/2079-6412/5/1/54
dc.identifier.urihttp://ir-library.mmust.ac.ke:8080/xmlui/handle/123456789/2257
dc.description.abstractIon layer gas reaction (ILGAR) method allows for deposition of Cl-containing and Cl-free In2S3 layers from InCl3 and In(OCCH3CHOCCH3)3 precursor salts, respectively. A comparative study was performed to investigate the role of Cl on the diffusion of Cu from CuSCN source layer into ILGAR deposited In2S3 layers. The Cl concentration was varied between 7 and 14 at.% by varying deposition parameters. The activation energies and exponential pre-factors for Cu diffusion in Cl-containing samples were between 0.70 to 0.78 eV and between 6.0 × 10−6 and 3.2 × 10−5 cm2/s. The activation energy in Cl-free ILGAR In2S3 layers was about three times less compared to the Cl-containing In2S3, and the pre-exponential constant six orders of magnitude lower. These values were comparable to those obtained from thermally evaporated In2S3 layers. The residual Cl-occupies S sites in the In2S3 structure leading to non-stoichiometry and hence different diffusion mechanism for Cu compared to stoichiometric Cl-free layers.en_US
dc.language.isoenen_US
dc.publishercoatingsen_US
dc.subjectRole of Cl on Diffusion of Cu in In2S3 Layers Prepared by Ion Layer Gas Reaction Methoden_US
dc.titleRole of Cl on Diffusion of Cu in In2S3 Layers Prepared by Ion Layer Gas Reaction Methoden_US
dc.typeArticleen_US


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