Surface-Originated Weak Confinement in Tetrahedral Indium Arsenide Quantum Dots

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dc.contributor.authorKim, Meereeko
dc.contributor.authorLEE, JUNHOko
dc.contributor.authorJung, Jae Gwanko
dc.contributor.authorShin, Daekwonko
dc.contributor.authorKim, Jugyoungko
dc.contributor.authorCho, Eunhyeko
dc.contributor.authorXing, Yaolongko
dc.contributor.authorJeong, Hyeonjunko
dc.contributor.authorPark, Seongminko
dc.contributor.authorOh, Sang Hoko
dc.contributor.authorKim, Yong-Hyunko
dc.contributor.authorJeong, Soheeko
dc.date.accessioned2024-04-23T07:00:12Z-
dc.date.available2024-04-23T07:00:12Z-
dc.date.created2024-04-23-
dc.date.created2024-04-23-
dc.date.created2024-04-23-
dc.date.issued2024-04-
dc.identifier.citationJOURNAL OF THE AMERICAN CHEMICAL SOCIETY, v.146, no.15, pp.10251 - 10256-
dc.identifier.issn0002-7863-
dc.identifier.urihttp://hdl.handle.net/10203/319202-
dc.description.abstractWhile the shape-dependent quantum confinement (QC) effect in anisotropic semiconductor nanocrystals has been extensively studied, the QC in facet-specified polyhedral quantum dots (QDs) remains underexplored. Recently, tetrahedral nanocrystals have gained prominence in III-V nanocrystal synthesis. In our study, we successfully synthesized well-faceted tetrahedral InAs QDs with a first excitonic absorption extending up to 1700 nm. We observed an unconventional sizing curve, indicating weaker confinement than for equivalently volumed spherical QDs. The (111) surface states of InAs QDs persist at the conduction band minimum state even after ligand passivation with a significantly reduced band gap, which places tetrahedral QDs at lower energies in the sizing curve. Consequently, films composed of tetrahedral QDs demonstrate an extended photoresponse into the short-wave infrared region, compared to isovolume spherical QD films.-
dc.languageEnglish-
dc.publisherAMER CHEMICAL SOC-
dc.titleSurface-Originated Weak Confinement in Tetrahedral Indium Arsenide Quantum Dots-
dc.typeArticle-
dc.identifier.wosid001200646000001-
dc.identifier.scopusid2-s2.0-85189913002-
dc.type.rimsART-
dc.citation.volume146-
dc.citation.issue15-
dc.citation.beginningpage10251-
dc.citation.endingpage10256-
dc.citation.publicationnameJOURNAL OF THE AMERICAN CHEMICAL SOCIETY-
dc.identifier.doi10.1021/jacs.4c00966-
dc.contributor.localauthorKim, Yong-Hyun-
dc.contributor.nonIdAuthorKim, Meeree-
dc.contributor.nonIdAuthorShin, Daekwon-
dc.contributor.nonIdAuthorKim, Jugyoung-
dc.contributor.nonIdAuthorCho, Eunhye-
dc.contributor.nonIdAuthorXing, Yaolong-
dc.contributor.nonIdAuthorJeong, Hyeonjun-
dc.contributor.nonIdAuthorPark, Seongmin-
dc.contributor.nonIdAuthorOh, Sang Ho-
dc.contributor.nonIdAuthorJeong, Sohee-
dc.description.isOpenAccessN-
dc.type.journalArticleArticle-
dc.subject.keywordPlusELECTRONIC-STRUCTURE-
dc.subject.keywordPlusINP-
dc.subject.keywordPlusSPECTROSCOPY-
dc.subject.keywordPlusPARTICLE-
dc.subject.keywordPlusSHAPE-
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