Electronic structure, orbital symmetry transformation, charge transfer, and valence state studies on Fe3+ - substituted CaCu3Ti4O12 quadruple perovskites using X-ray photoelectron spectroscopy
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Meshiya, Urmila M. | - |
dc.contributor.author | Raval, Pooja Y. | - |
dc.contributor.author | Pansara, Pooja R. | - |
dc.contributor.author | Nehra, Monika | - |
dc.contributor.author | Jakhar, Narendra | - |
dc.contributor.author | Kumar, Sandeep | - |
dc.contributor.author | Modi, Kunal B. | - |
dc.contributor.author | Lim, Dong-Kwon | - |
dc.contributor.author | Singhal, Rishi Kumar | - |
dc.date.accessioned | 2021-08-31T10:54:10Z | - |
dc.date.available | 2021-08-31T10:54:10Z | - |
dc.date.created | 2021-06-19 | - |
dc.date.issued | 2020-02-01 | - |
dc.identifier.issn | 0272-8842 | - |
dc.identifier.uri | https://scholar.korea.ac.kr/handle/2021.sw.korea/57718 | - |
dc.description.abstract | Here, we report a detailed study on electronic structure of quadruple perovskite system, CaCu3Ti4O12 (x = 0.0, 0.1, 0.3, 0.5 and 0.7), using the powerful X-ray photoelectron spectroscopy (XPS). The Ca2p and Ti2p XPS spectra indicate that Ca and Ti ions exist in the divalent and tetravalent state, respectively, and no visible change is observed in their valence states on Fe3+-substitution (x). The asymmetrically shaped peaks of Ti(2)p(3/2) infer the significant orbital hybridization of Ti atoms with other metallic cations like Cu and Fe, i.e. the Ti2p-Cu3d-Fe3d mixed states, which shows an increment with the Fe3+-content. The spectra also indicate that the Fesubstitution causes an increase in the strength of CuFe3d-O2p hybridization while weakening the strength of TiFe3d-O2p orbital hybridization. The Cu2p spectra suggest that Cu ions exist in two valence states i.e. the Cu2+ and Cu3+ out of which Cu2+ is dominant. The XPS results show clear evidence of charge transfer amongst Ti-Cu ions and evolution of n-type charge carriers. The O1s XPS spectra indicate anti-bonding states of t(2g) and e(g) type molecular orbitals separated by an energy separation of similar to 1.6 eV. A systematic relative change in the intensity of t(2g) and e(g) peaks with Fe-substitution point towards a clear transformation of symmetry of the system from TiO6 octahedral to the square-planar. | - |
dc.language | English | - |
dc.language.iso | en | - |
dc.publisher | ELSEVIER SCI LTD | - |
dc.subject | DIELECTRIC-PROPERTIES | - |
dc.subject | ELECTRICAL BEHAVIOR | - |
dc.subject | MAGNETIC-PROPERTIES | - |
dc.title | Electronic structure, orbital symmetry transformation, charge transfer, and valence state studies on Fe3+ - substituted CaCu3Ti4O12 quadruple perovskites using X-ray photoelectron spectroscopy | - |
dc.type | Article | - |
dc.contributor.affiliatedAuthor | Lim, Dong-Kwon | - |
dc.identifier.doi | 10.1016/j.ceramint.2019.09.198 | - |
dc.identifier.scopusid | 2-s2.0-85072643471 | - |
dc.identifier.wosid | 000527383100103 | - |
dc.identifier.bibliographicCitation | CERAMICS INTERNATIONAL, v.46, no.2, pp.2147 - 2154 | - |
dc.relation.isPartOf | CERAMICS INTERNATIONAL | - |
dc.citation.title | CERAMICS INTERNATIONAL | - |
dc.citation.volume | 46 | - |
dc.citation.number | 2 | - |
dc.citation.startPage | 2147 | - |
dc.citation.endPage | 2154 | - |
dc.type.rims | ART | - |
dc.type.docType | Article | - |
dc.description.journalClass | 1 | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
dc.relation.journalResearchArea | Materials Science | - |
dc.relation.journalWebOfScienceCategory | Materials Science, Ceramics | - |
dc.subject.keywordPlus | DIELECTRIC-PROPERTIES | - |
dc.subject.keywordPlus | ELECTRICAL BEHAVIOR | - |
dc.subject.keywordPlus | MAGNETIC-PROPERTIES | - |
dc.subject.keywordAuthor | Calcium-copper-titanate | - |
dc.subject.keywordAuthor | X-ray photoelectron spectroscopy | - |
dc.subject.keywordAuthor | Electronic structure | - |
dc.subject.keywordAuthor | Orbital symmetry transformation | - |
Items in ScholarWorks are protected by copyright, with all rights reserved, unless otherwise indicated.
145 Anam-ro, Seongbuk-gu, Seoul, 02841, Korea+82-2-3290-2963
COPYRIGHT © 2021 Korea University. All Rights Reserved.
Certain data included herein are derived from the © Web of Science of Clarivate Analytics. All rights reserved.
You may not copy or re-distribute this material in whole or in part without the prior written consent of Clarivate Analytics.