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dc.contributor.authorYAN, Hen_US
dc.contributor.authorQin, Men_US
dc.contributor.authorGao, Fen_US
dc.contributor.authorCizek, Jen_US
dc.contributor.authorYang, Sen_US
dc.contributor.authorFan, Xen_US
dc.contributor.authorZhao, Len_US
dc.contributor.authorXu, Jen_US
dc.contributor.authorDong, Gen_US
dc.contributor.authorREECE, Men_US
dc.date.accessioned2018-10-30T15:32:05Z
dc.date.available2018-10-11en_US
dc.date.issued2018-10-13en_US
dc.date.submitted2018-10-26T15:02:56.830Z
dc.identifier.urihttp://qmro.qmul.ac.uk/xmlui/handle/123456789/49365
dc.description.abstractSr1-xLaxTiO3 (SLTO) ceramics with colossal permittivity were fabricated by conventional solid-state reaction method. The point defects of pure STO and SLTO ceramics were analyzed by Positron Annihilation Lifetime Spectroscopy (PALS) and Coincidence Doppler Broadening (CDB). The charge compensation mechanisms and dielectric properties of ceramics were investigated. The results indicated that the intrinsic defects in pure STO ceramics were mainly V00 00 Ti . The charge compensation mechanism of SLTO ceramics was predominantly formation of V00 Sr . With increasing La content, εr of SLTO ceramics increased up to ~70000 at room temperature. The results of first-principle calculations indicated that the colossal permittivity came from a sharp polarization increase caused by dipole structure of defects. tand of SLTO ceramics showed obvious Debye relaxation at high temperatures and the relaxation showed a multiple relaxation times derived from different kinds of polarization mechanism. The main polarization mechanism of SLTO ceramics gradually changed from ion displacement polarization to defect dipole polarization influenced by the concentration of La dopants.en_US
dc.format.extent76 - 89en_US
dc.relation.ispartofActa Materialiaen_US
dc.rightshttps://doi.org/10.1016/j.actamat.2018.10.025
dc.titlePoint defect structure of La-doped SrTiO3 ceramics with colossal permittivityen_US
dc.typeArticle
dc.rights.holder© 2018 Acta Materialia Inc.
dc.identifier.doi10.1016/j.actamat.2018.10.025en_US
pubs.notesNot knownen_US
pubs.publication-statusPublisheden_US
pubs.volume164en_US
dcterms.dateAccepted2018-10-11en_US


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