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dc.contributor.authorPustovarov, V. A.en
dc.contributor.authorSmirnova, T. P.en
dc.contributor.authorLebedev, M. S.en
dc.contributor.authorGritsenko, V. A.en
dc.contributor.authorKirm, M.en
dc.date.accessioned2021-08-31T15:03:12Z-
dc.date.available2021-08-31T15:03:12Z-
dc.date.issued2016-
dc.identifier.citationIntrinsic and defect related luminescence in double oxide films of Al-Hf-O system under soft X-ray and VUV excitation / V. A. Pustovarov, T. P. Smirnova, M. S. Lebedev, et al. — DOI 10.1016/j.jlumin.2015.10.053 // Journal of Luminescence. — 2016. — Vol. 170. — P. 161-167.en
dc.identifier.issn222313-
dc.identifier.otherFinal2
dc.identifier.otherAll Open Access, Green3
dc.identifier.otherhttps://www.scopus.com/inward/record.uri?eid=2-s2.0-84946601313&doi=10.1016%2fj.jlumin.2015.10.053&partnerID=40&md5=a18f36266da7b66d6c20c6521e1ff19d
dc.identifier.otherhttp://bib-pubdb1.desy.de/record/291757/files/Accepdet%20manuscript.pdfm
dc.identifier.urihttp://elar.urfu.ru/handle/10995/102334-
dc.description.abstractLow temperature time-resolved luminescence spectra in the region of 2.5-9.5 eV under soft X-ray excitation as well as time-resolved luminescence excitation spectra in the UV-VUV region (3.7-12 eV) of solid solutions AlxHfyO1-x-y thin films were investigated. The values of x and Al/Hf ratio were determined from X-ray photoelectron srectroscopy data. Hafnia films and films mixed with alumina were grown in a flow-type chemical vapor deposition reactor with argon as a carrier gas. In addition, pure alumina films were prepared by the atomic layer deposition method. A strong emission band with the peak position at 4.4 eV and with the decay time in the μs-range was revealed for pure hafnia films. The emission peak at 7.74 eV with short nanosecond decay kinetics was observed in the luminescence spectra for pure alumina films. These emission bands were ascribed to the radiative decay of self-trapped excitons (an intrinsic luminescence) in pure HfO2 and Al2O3 films, respectively. Along with intrinsic host emission, defect related luminescence bands with a larger Stokes shift were observed. In the emission spectra of the solid solution films (x=4; 17; 20 at%) the intrinsic emission bands are quenched and only the luminescence of defects (an anion vacancies) was observed. Based on transformation of the luminescence spectra and ns-luminescence decay kinetics, as well as changes in the time-resolved luminescence and luminescence excitation spectra, the relaxation processes in the films of solid solution are discussed. © 2015 Elsevier B.V. All rights reserved.en
dc.format.mimetypeapplication/pdfen
dc.language.isoenen
dc.publisherElsevieren
dc.rightsinfo:eu-repo/semantics/openAccessen
dc.sourceJ Lumin2
dc.sourceJournal of Luminescenceen
dc.subjectALUMINAen
dc.subjectDEFECTSen
dc.subjectHAFNIAen
dc.subjectSELF-TRAPPED EXCITONen
dc.subjectTHIN FILMSen
dc.subjectTIME-RESOLVED LUMINESCENCEen
dc.subjectALUMINAen
dc.subjectALUMINUMen
dc.subjectARGONen
dc.subjectATOMIC LAYER DEPOSITIONen
dc.subjectCHEMICAL VAPOR DEPOSITIONen
dc.subjectDEFECTSen
dc.subjectDEPOSITIONen
dc.subjectEMISSION SPECTROSCOPYen
dc.subjectEXCITED STATESen
dc.subjectEXCITONSen
dc.subjectHAFNIUMen
dc.subjectHAFNIUM OXIDESen
dc.subjectLIGHT EMISSIONen
dc.subjectLUMINESCENCEen
dc.subjectPOTASSIUM COMPOUNDSen
dc.subjectSOLID SOLUTIONSen
dc.subjectTEMPERATUREen
dc.subjectTHIN FILMSen
dc.subjectVAPOR DEPOSITIONen
dc.subjectCHEMICAL VAPOR DEPOSITION REACTORSen
dc.subjectHAFNIAen
dc.subjectINTRINSIC LUMINESCENCEen
dc.subjectLUMINESCENCE DECAY KINETICSen
dc.subjectLUMINESCENCE EXCITATION SPECTRAen
dc.subjectSELF TRAPPED EXCITONSen
dc.subjectTIME-RESOLVED LUMINESCENCEen
dc.subjectTIME-RESOLVED LUMINESCENCE SPECTRAen
dc.subjectOXIDE FILMSen
dc.titleIntrinsic and defect related luminescence in double oxide films of Al-Hf-O system under soft X-ray and VUV excitationen
dc.typeArticleen
dc.typeinfo:eu-repo/semantics/articleen
dc.typeinfo:eu-repo/semantics/publishedVersionen
dc.identifier.doi10.1016/j.jlumin.2015.10.053-
dc.identifier.scopus84946601313-
local.contributor.employeePustovarov, V.A., Ural Federal University, 19 Mira Street, Yekaterinburg, 620002, Russian Federation
local.contributor.employeeSmirnova, T.P., Nikolaev Institute of Inorganic Chemistry, Siberian Branch, Russian Academy of Science, Novosibirsk, 630090, Russian Federation
local.contributor.employeeLebedev, M.S., Nikolaev Institute of Inorganic Chemistry, Siberian Branch, Russian Academy of Science, Novosibirsk, 630090, Russian Federation
local.contributor.employeeGritsenko, V.A., Institute of Semiconductor Physics, Siberian Branch, Russian Academy of Sciences, Novosibirsk, 630090, Russian Federation, Novosibirsk National Research University, 2 Pirogova Street, Novosibirsk, 630090, Russian Federation
local.contributor.employeeKirm, M., Institute of Physics, University of Tartu, 14c Ravila, Tartu, 50411, Estonia
local.description.firstpage161-
local.description.lastpage167-
local.volume170-
dc.identifier.wos000365606600023-
local.contributor.departmentUral Federal University, 19 Mira Street, Yekaterinburg, 620002, Russian Federation
local.contributor.departmentNikolaev Institute of Inorganic Chemistry, Siberian Branch, Russian Academy of Science, Novosibirsk, 630090, Russian Federation
local.contributor.departmentInstitute of Semiconductor Physics, Siberian Branch, Russian Academy of Sciences, Novosibirsk, 630090, Russian Federation
local.contributor.departmentNovosibirsk National Research University, 2 Pirogova Street, Novosibirsk, 630090, Russian Federation
local.contributor.departmentInstitute of Physics, University of Tartu, 14c Ravila, Tartu, 50411, Estonia
local.identifier.pureb9e4fe7c-175f-4e57-83be-e762d5645f27uuid
local.identifier.pure605144-
local.identifier.eid2-s2.0-84946601313-
local.identifier.wosWOS:000365606600023-
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