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Zastosuj identyfikator do podlinkowania lub zacytowania tej pozycji: http://hdl.handle.net/20.500.12128/11074
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dc.contributor.authorRogala, M.-
dc.contributor.authorBihlmayer, G.-
dc.contributor.authorDąbrowski, P.-
dc.contributor.authorRodenbücher, C.-
dc.contributor.authorWrana, D.-
dc.contributor.authorKrok, F.-
dc.contributor.authorKlusek, Z.-
dc.contributor.authorSzot, Krzysztof-
dc.date.accessioned2019-09-27T11:26:37Z-
dc.date.available2019-09-27T11:26:37Z-
dc.date.issued2019-
dc.identifier.citation"Scientific Reports (Nature Publishing Group)" Vol. 9, art. no 12563, s. 1-9pl_PL
dc.identifier.issn2045-2322-
dc.identifier.urihttp://hdl.handle.net/20.500.12128/11074-
dc.description.abstractWe investigate the thermal reduction of TiO2 in ultra-high vacuum. Contrary to what is usually assumed, we observe that the maximal surface reduction occurs not during the heating, but during the cooling of the sample back to room temperature. We describe the self-reduction, which occurs as a result of differences in the energies of defect formation in the bulk and surface regions. The findings presented are based on X-ray photoelectron spectroscopy carried out in-operando during the heating and cooling steps. The presented conclusions, concerning the course of redox processes, are especially important when considering oxides for resistive switching and neuromorphic applications and also when describing the mechanisms related to the basics of operation of solid oxide fuel cells.pl_PL
dc.language.isoenpl_PL
dc.rightsUznanie autorstwa 3.0 Polska*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/pl/*
dc.subjectthermal reductionpl_PL
dc.subjectTiO2pl_PL
dc.subjectcrystalpl_PL
dc.subjectspectroscopypl_PL
dc.titleSelf-reduction of the native TiO2(110) surface during cooling after thermal annealing - in-operando investigationspl_PL
dc.typeinfo:eu-repo/semantics/articlepl_PL
dc.identifier.doi10.1038/s41598-019-48837-3-
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Uznanie Autorstwa 3.0 Polska Creative Commons Creative Commons