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dc.contributor.authorJoung, Mi-Ri-
dc.contributor.authorSeo, In-Tae-
dc.contributor.authorKim, Jin-Seong-
dc.contributor.authorXu, HaiBo-
dc.contributor.authorHan, Guifang-
dc.contributor.authorKang, Min-Gyu-
dc.contributor.authorKang, Chong-Yun-
dc.contributor.authorYoon, Seok-Jin-
dc.contributor.authorNahm, Sahn-
dc.date.accessioned2024-01-20T12:04:51Z-
dc.date.available2024-01-20T12:04:51Z-
dc.date.created2021-09-05-
dc.date.issued2013-06-
dc.identifier.issn1359-6454-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/128013-
dc.description.abstractBecause of the presence of OH- and H2O in the KN unit cell, tetragonal KNbO3 (KN) nanowires were formed when the synthesis was carried out at 120 degrees C for 48 h. However, when the fabrication was conducted at high temperatures (>= 150 degrees C) or at 120 degrees C for a long period of time (>= 72 h), orthorhombic KN nanowires were formed. Moreover, the KN nanowires synthesized at 120 degrees C for 60 h showed a morphotropic phase boundary (MPB) structure in which both tetragonal and orthorhombic structures coexisted. Tetragonal, orthorhombic and MPB KN nanowires were also grown on the Nb5+-doped SrTiO3 substrate, and their d(33) values were measured for the first time. A tetragonal KN nanowire exhibited a d(33) value of 23.5 pm V-1, which is larger than that of the orthorhombic KN nanowire (11.6 pm V-1), probably because of the softening effect of the metal vacancies. The MPB KN nanowires exhibited a larger d33 value of 40.0 pm V-1. The d(33) values of KN nanowires increased to 104.5, 137.1 and 146.0 pm V-1 for the orthorhombic, tetragonal and MPB KN nanowires, respectively, after the KN nanowires were poled along the [1 0 0] direction by application of a DC voltage of 10 V. (C) 2013 Acta Materialia Inc. Published by Elsevier Ltd. All rights reserved.-
dc.languageEnglish-
dc.publisherPERGAMON-ELSEVIER SCIENCE LTD-
dc.subjectNANOGENERATORS-
dc.subjectPEROVSKITE-
dc.subjectGROWTH-
dc.titleStructural dependence of the piezoelectric properties of KNbO3 nanowires synthesized by the hydrothermal method-
dc.typeArticle-
dc.identifier.doi10.1016/j.actamat.2013.03.002-
dc.description.journalClass1-
dc.identifier.bibliographicCitationACTA MATERIALIA, v.61, no.10, pp.3703 - 3708-
dc.citation.titleACTA MATERIALIA-
dc.citation.volume61-
dc.citation.number10-
dc.citation.startPage3703-
dc.citation.endPage3708-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000319304400015-
dc.identifier.scopusid2-s2.0-84876946020-
dc.relation.journalWebOfScienceCategoryMaterials Science, Multidisciplinary-
dc.relation.journalWebOfScienceCategoryMetallurgy & Metallurgical Engineering-
dc.relation.journalResearchAreaMaterials Science-
dc.relation.journalResearchAreaMetallurgy & Metallurgical Engineering-
dc.type.docTypeArticle-
dc.subject.keywordPlusNANOGENERATORS-
dc.subject.keywordPlusPEROVSKITE-
dc.subject.keywordPlusGROWTH-
dc.subject.keywordAuthorPiezoelectricity-
dc.subject.keywordAuthorNanowire-
dc.subject.keywordAuthorPerovskites-
dc.subject.keywordAuthorSynthesis-
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KIST Article > 2013
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