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A study of the red-shift of a neutral donor bound exciton in GaN nanorods by hydrogenation

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dc.contributor.authorPark, Byung-Guon-
dc.contributor.authorLee, Sang-Tae-
dc.contributor.authorReddeppa, Maddaka-
dc.contributor.authorKim, Moon-Deock-
dc.contributor.authorOh, Jae-Eung-
dc.contributor.authorLee, Sang-Kwon-
dc.date.accessioned2021-06-22T13:42:09Z-
dc.date.available2021-06-22T13:42:09Z-
dc.date.issued2017-09-
dc.identifier.issn0957-4484-
dc.identifier.issn1361-6528-
dc.identifier.urihttps://scholarworks.bwise.kr/erica/handle/2021.sw.erica/8972-
dc.description.abstractIn this paper we account for the physics behind the exciton peak shift in GaN nanorods (NRs) due to hydrogenation. GaN NRs were selectively grown on a patterned Ti/Si(111) substrate using plasma-assisted molecular beam epitaxy, and the effect of hydrogenation on their optical properties was investigated in detail using low-temperature photoluminescence measurements. Due to hydrogenation, the emissions corresponding to the donor-acceptor pair and yellow luminescence in GaN NRs were strongly suppressed, while the emission corresponding to the neutral to donor bound exciton ((DX)-X-0) exhibited red-shift. Thermal annealing of hydrogenated GaN NRs demonstrated the recovery of the (DX)-X-0 and deep level emission. To determine the nature of the D0X peak shift due to hydrogenation, comparative studies were carried out on various diameters of GaN NRs, which can be controlled by different growth conditions and wet-etching times. Our experimental results reveal that the (DX)-X-0 shift depends on the diameter of the GaN NRs after hydrogenation. The results clearly demonstrate that the hydrogenation leads to band bending of GaN NRs as compensated by hydrogen ions, which causes a red-shift in the (DX)-X-0 emission.-
dc.language영어-
dc.language.isoENG-
dc.publisherIOP PUBLISHING LTD-
dc.titleA study of the red-shift of a neutral donor bound exciton in GaN nanorods by hydrogenation-
dc.typeArticle-
dc.publisher.location영국-
dc.identifier.doi10.1088/1361-6528/aa7b9a-
dc.identifier.scopusid2-s2.0-85028311788-
dc.identifier.wosid000407455700002-
dc.identifier.bibliographicCitationNANOTECHNOLOGY, v.28, no.36-
dc.citation.titleNANOTECHNOLOGY-
dc.citation.volume28-
dc.citation.number36-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClasssci-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaScience & Technology - Other Topics-
dc.relation.journalResearchAreaMaterials Science-
dc.relation.journalResearchAreaPhysics-
dc.relation.journalWebOfScienceCategoryNanoscience & Nanotechnology-
dc.relation.journalWebOfScienceCategoryMaterials Science, Multidisciplinary-
dc.relation.journalWebOfScienceCategoryPhysics, Applied-
dc.subject.keywordPlusDEEP LEVELS-
dc.subject.keywordPlusYELLOW LUMINESCENCE-
dc.subject.keywordPlusFILMS-
dc.subject.keywordPlusEPILAYERS-
dc.subject.keywordAuthornanorods-
dc.subject.keywordAuthorhydrogenation-
dc.subject.keywordAuthorneutral donor bound exciton-
dc.subject.keywordAuthorband bending-
dc.identifier.urlhttps://iopscience.iop.org/article/10.1088/1361-6528/aa7b9a-
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