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Misidentification of hexagonal phase as barium carbonate during chemical synthesis of barium titanate nanopowders

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dc.contributor.authorSelvaraj, M.
dc.contributor.authorVenkatesan, R.
dc.contributor.authorMayandi, J.
dc.contributor.authorVenkatachalapathy, V.
dc.contributor.authorВенкатачалапатху, Вишнукантхан
dc.date.accessioned2024-11-21T18:29:18Z
dc.date.available2024-11-21T18:29:18Z
dc.date.issued2019
dc.description.abstractBarium titanate (BaTiO3) nanopowders were synthesized by combining two facile route namely so-gel and hydrothermal process. The samples synthesized at 100 and 200 degrees C are found to exhibit cubic crystalline structure and mixed tetragonal and orthorhombic phases, respectively, as analyzed from XRD studies. In addition, characteristic peaks of unknown phase often identified as barium carbonate (BaCO3) was also observed. Post-annealing treatment suggests stabilization of hexagonal BaTiO3, confirmed by XRD and Raman studies. (C) 2019 Elsevier Ltd. Peer-review under responsibility of the scientific committee of the Advanced Materials for Clean Energy and Health Applications (AMCEHA).
dc.format.extentС. 81-84
dc.identifier.citationMisidentification of hexagonal phase as barium carbonate during chemical synthesis of barium titanate nanopowders / Selvaraj, M [et al.] // Materials Today: Proceedings. - 2019. - 23. - P. 81-84. - 10.1016/j.matpr.2019.06.713
dc.identifier.doi10.1016/j.matpr.2019.06.713
dc.identifier.urihttps://www.doi.org/10.1016/j.matpr.2019.06.713
dc.identifier.urihttps://www.scopus.com/record/display.uri?eid=2-s2.0-85084224610&origin=resultslist
dc.identifier.urihttp://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=Alerting&SrcApp=Alerting&DestApp=WOS_CPL&DestLinkType=FullRecord&UT=WOS:000520866900018
dc.identifier.urihttps://openrepository.mephi.ru/handle/123456789/19515
dc.relation.ispartofMaterials Today: Proceedings
dc.titleMisidentification of hexagonal phase as barium carbonate during chemical synthesis of barium titanate nanopowders
dc.typeConference Paper
dspace.entity.typePublication
oaire.citation.volume23
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