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dc.contributor.authorSong, JH-
dc.contributor.authorKim, JW-
dc.contributor.authorPark, MJ-
dc.contributor.authorKim, JS-
dc.contributor.authorJung, KU-
dc.contributor.authorSuh, SH-
dc.date.accessioned2024-01-21T17:32:25Z-
dc.date.available2024-01-21T17:32:25Z-
dc.date.created2021-09-04-
dc.date.issued1998-02-
dc.identifier.issn0022-0248-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/143273-
dc.description.abstractWe report in situ n- and p-type doping of HgCdTe/CdTe/(1 0 0)GaAs grown by metalorganic vapor phase epitaxy (MOVPE), using the interdiffused multilayer process (IMP). HgCdTe was doped either with iodine from isopropyliodide (IPI) for n-type doping or with arsenic from tris-dimethylaminoarsenic (DMAAs) for p-type doping. Standard bubbler configurations were used for dopant precursors. DiPTe, DmCd and elemental Hg were used as sources. HgCdTe layers of 10 mu m were grown on (1 0 0)GaAs at 370 degrees C. Dopant gases were allowed into the reactor only during the CdTe growth cycle of the IMP process. HgCdTe layers were Hg-annealed at 415 degrees C for 15 min and at 220 degrees C for 3 h, consecutively. Iodine-doped HgCdTe layers had 77 K electron concentrations of 6 x 10(15) to 5 x 10(17) cm(-3). Hall mobility decreased with increasing doping concentration. Arsenic-doped PgCdTe layers had 77 K hole concentration of 2 x 10(16) to 7 x 10(17) cm(-3) with about 100% of arsenic activated. Composition x of Hg1-xCdxTe layers was not influenced by the arsenic doping. The above results show that IPI and DMAAs precursors are excellent n- and p-doping sources for HgCdTe. (C) 1998 Elsevier Science B.V. All rights reserved.-
dc.languageEnglish-
dc.publisherELSEVIER SCIENCE BV-
dc.subjectDEPOSITION-
dc.subjectHGCDTE-
dc.titleIodine and arsenic doping of (100)HgCdTe/GaAs grown by metalorganic vapor phase epitaxy using isopropyl iodide and tris-dimethylaminoarsenic-
dc.typeArticle-
dc.description.journalClass1-
dc.identifier.bibliographicCitationJOURNAL OF CRYSTAL GROWTH, v.184, pp.1232 - 1236-
dc.citation.titleJOURNAL OF CRYSTAL GROWTH-
dc.citation.volume184-
dc.citation.startPage1232-
dc.citation.endPage1236-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000072653800254-
dc.identifier.scopusid2-s2.0-0000187823-
dc.relation.journalWebOfScienceCategoryCrystallography-
dc.relation.journalWebOfScienceCategoryMaterials Science, Multidisciplinary-
dc.relation.journalWebOfScienceCategoryPhysics, Applied-
dc.relation.journalResearchAreaCrystallography-
dc.relation.journalResearchAreaMaterials Science-
dc.relation.journalResearchAreaPhysics-
dc.type.docTypeArticle; Proceedings Paper-
dc.subject.keywordPlusDEPOSITION-
dc.subject.keywordPlusHGCDTE-
dc.subject.keywordAuthoriodine-
dc.subject.keywordAuthorarsenic-
dc.subject.keywordAuthordoping-
dc.subject.keywordAuthorHgCdTe-
dc.subject.keywordAuthorMOVPE-
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