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dc.contributor.authorPark, Seong Gon-
dc.contributor.authorLee, Kyu Hyoung-
dc.contributor.authorLee, Jae-Hoon-
dc.contributor.authorBang, Geukchan-
dc.contributor.authorKim, Junghwan-
dc.contributor.authorPark, Hee Jung-
dc.contributor.authorOh, Min Suk-
dc.contributor.authorLee, Suyoun-
dc.contributor.authorKim, Young-Hoon-
dc.contributor.authorKim, Young-Min-
dc.contributor.authorHosono, Hideo-
dc.contributor.authorBang, Joonho-
dc.contributor.authorLee, Kimoon-
dc.date.accessioned2024-01-19T18:03:15Z-
dc.date.available2024-01-19T18:03:15Z-
dc.date.created2021-09-05-
dc.date.issued2020-02-21-
dc.identifier.issn2052-1553-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/118943-
dc.description.abstractThe origin of the electrical and optical properties of Cu-substituted NiO (Cu : NiO) polycrystalline bulks synthesized via a solid-state reaction is reported. The partial substitution of Ni sites with Cu led to a drastic decrease of the electrical resistivity from 7.73 x 10(8) to 6.51 x 10(4) Omega cm and a reduction in the energy for the self-trapping barrier from 0.58 to 0.24 eV in accordance with small polaron hopping conduction. The well-sustained band gap of 3.1 eV and antiferromagnetic transition temperature of 453 K demonstrate that the strength of the electron correlation in NiO can persist even at a high Cu concentration up to 22 atomic percent. Density functional theory calculations confirm that the Cu 3d orbital encourages d-p hybridization between metal cations and oxygen anions at the valence band maximum. As a consequence, this hybridization plays a critical role in improving the polaron hopping efficiency without much suppression of the Mott-Hubbard interaction and thus retaining the wide band gap nature.-
dc.languageEnglish-
dc.publisherROYAL SOC CHEMISTRY-
dc.subjectTEMPERATURE-
dc.subjectCONDUCTION-
dc.titleImproved polaronic transport under a strong Mott-Hubbard interaction in Cu-substituted NiO-
dc.typeArticle-
dc.identifier.doi10.1039/c9qi01052a-
dc.description.journalClass1-
dc.identifier.bibliographicCitationINORGANIC CHEMISTRY FRONTIERS, v.7, no.4, pp.853 - 858-
dc.citation.titleINORGANIC CHEMISTRY FRONTIERS-
dc.citation.volume7-
dc.citation.number4-
dc.citation.startPage853-
dc.citation.endPage858-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000515601600023-
dc.identifier.scopusid2-s2.0-85080032853-
dc.relation.journalWebOfScienceCategoryChemistry, Inorganic & Nuclear-
dc.relation.journalResearchAreaChemistry-
dc.type.docTypeArticle-
dc.subject.keywordPlusTEMPERATURE-
dc.subject.keywordPlusCONDUCTION-
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KIST Article > 2020
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