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Photoluminescence dynamics and quantum yield of intrinsically conductive ZnO from atomic layer deposition

dc.contributor.authorBeh, Holger
dc.contributor.authorHiller, Daniel
dc.contributor.authorSalava, Jan
dc.contributor.authorTrojánek, František
dc.contributor.authorZacharias, Margit
dc.contributor.authorMalý, Petr
dc.contributor.authorValenta, Jan
dc.date.accessioned2018-05-24T05:15:02Z
dc.date.issued2018
dc.description.abstractZinc oxide (ZnO) thin films deposited by atomic layer deposition (ALD) and a (0001)-oriented bulk-ZnO single-crystal are compared by ultrafast time-resolved and spectral photoluminescence spectroscopy as well as by luminescence quantum yield (QY) measurements. While the ALD-ZnO is intrinsically conductive, bulk-ZnO is electrically rather insulating. Nevertheless, PL spectra of both materials reveal similarities: A peak in the near-UV originating from inter-band transitions and a defect peak in the green-yellow spectral region associated to deep trap states. We investigate the dynamics and efficiency of these luminescence emissions to understand the interdependency of defects and the yet insufficiently understood conductivity mechanism of ALD-ZnO. Spectrally, a PL blueshift of the trap-mediated peak is observed for the transition from poor to good conductivity, which occurs with increasing ALD-deposition temperature. The quantum yield of ALD-ZnO is shown to be ~ 18-times lower and the luminescence lifetime of the UV-peak is ~ 14-times shorter compared to bulk-ZnO. We conclude that these properties are related to a significantly higher density of non-radiative defects, which might also represent electrically active scattering centers. These results indicate a new direction for further optimization of ALD-ZnO towards indium tin oxide (ITO)-compatible electrical conductivities by reducing or passivating these defects.en_AU
dc.description.sponsorshipH.B. acknowledges funding by the graduate school “decentralizedsustainable energy systems (DENE).” D.H. thanks the Alexander vonHumboldt Foundation for a Feodor Lynen Fellowship. This work wassupported by the bilateral Czech-German DFG-GACR project 16-09745Jand ZA 191/36-1en_AU
dc.format.mimetypeapplication/pdfen_AU
dc.identifier.issn0022-2313en_AU
dc.identifier.urihttp://hdl.handle.net/1885/143595
dc.rightshttp://www.sherpa.ac.uk/romeo/issn/0022-2313/..."Author's post-print on open access repository after an embargo period of between 12 months and 48 months" from SHERPA/RoMEO site (as at 24/05/18). This manuscript version is made available under the CC-BY-NC-ND 4.0 license http://creativecommons.org/licenses/by-nc-nd/4.0/en_AU
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.sourceJournal of Luminescenceen_AU
dc.subjectZinc oxideen_AU
dc.subjectTime-resolved photoluminescenceen_AU
dc.subjectAtomic layer depositionen_AU
dc.subjectQuantum yielden_AU
dc.titlePhotoluminescence dynamics and quantum yield of intrinsically conductive ZnO from atomic layer depositionen_AU
dc.typeJournal articleen_AU
dcterms.accessRightsOpen Accessen_AU
local.bibliographicCitation.lastpage89en_AU
local.bibliographicCitation.startpage85en_AU
local.contributor.affiliationHiller, D., Research School of Engineering, The Australian National Universityen_AU
local.contributor.authoruidu1049396en_AU
local.identifier.citationvolume201en_AU
local.identifier.doi10.1016/j.jlumin.2018.04.044en_AU
local.type.statusAccepted Versionen_AU

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