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Layered Bismuth Oxyfluoride Nitrates Revealing Large Second-Harmonic Generation and Photocatalytic Properties

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dc.contributor.authorCho, Eun Jeong-
dc.contributor.authorOh, Seung-Jin-
dc.contributor.authorJo, Hongil-
dc.contributor.authorLee, Junsu-
dc.contributor.authorYou, Tae-Soo-
dc.contributor.authorOk, Kang Min-
dc.date.available2019-05-28T01:37:48Z-
dc.date.issued2019-02-
dc.identifier.issn0020-1669-
dc.identifier.issn1520-510X-
dc.identifier.urihttps://scholarworks.bwise.kr/cau/handle/2019.sw.cau/18238-
dc.description.abstractTwo novel bismuth oxyfluoride nitrates, Bi2OF3(NO3) and Bi6O6F5(NO3), have been synthesized via hydrothermal reactions. Whereas Bi2OF3(NO3) crystallizes in the centrosymmetric (CS) hexagonal space group, P6(3)/m, Bi6O6F5(NO3) crystallizes in the polar noncentrosymmetric (NCS) trigonal space group, R3. The backbones of the title compounds reveal double layered structures composed of asymmetric BiF3(O/F)(3) or BiO3F2 polyhedra and NO3 trigonal planar groups. The diffuse reflectance spectra indicate that Bi2OF3(NO3) and Bi6O6F5(NO3) contain wide band gaps of 3.5 and 4.0 eV, respectively. Powder second-harmonic generation (SHG) measurements suggest that NCS Bi6O6F5(NO3) is Type-I phase-matchable and has a large SHG response of ca. 3 times that of KH2PO4 (KDP). Electron localization function (ELF) analysis indicates that the large SHG efficiency of Bi6O6F5(NO3) is attributed to the synergistic effect of the alignment of NO3- trigonal planar groups and strong interactions between highly polarizable lone pair electrons on Bi3+ and pi-delocalized electrons in NO3- groups. Bi2OF3(NO3) also exhibits a very good photocatalytic degradation efficiency of Rhodamine B (RhB) under the UV light irradiation.-
dc.format.extent8-
dc.language영어-
dc.language.isoENG-
dc.publisherAMER CHEMICAL SOC-
dc.titleLayered Bismuth Oxyfluoride Nitrates Revealing Large Second-Harmonic Generation and Photocatalytic Properties-
dc.typeArticle-
dc.identifier.doi10.1021/acs.inorgchem.8b03343-
dc.identifier.bibliographicCitationINORGANIC CHEMISTRY, v.58, no.3, pp 2183 - 2190-
dc.description.isOpenAccessN-
dc.identifier.wosid000458085900052-
dc.identifier.scopusid2-s2.0-85061067566-
dc.citation.endPage2190-
dc.citation.number3-
dc.citation.startPage2183-
dc.citation.titleINORGANIC CHEMISTRY-
dc.citation.volume58-
dc.type.docTypeArticle-
dc.publisher.location미국-
dc.subject.keywordPlusBOND-VALENCE PARAMETERS-
dc.subject.keywordPlusCRYSTAL-STRUCTURE-
dc.subject.keywordPlusNONCENTROSYMMETRIC MATERIALS-
dc.subject.keywordPlusBASIC NITRATE-
dc.subject.keywordPlusBI2O2(OH)(NO3)-
dc.subject.keywordPlusHYDROLYSIS-
dc.subject.keywordPlusBI5O7NO3-
dc.subject.keywordPlusPOLARITY-
dc.subject.keywordPlusDESIGN-
dc.subject.keywordPlusSIZE-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalWebOfScienceCategoryChemistry, Inorganic & Nuclear-
dc.description.journalRegisteredClasssci-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
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