Full metadata record
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Kuo, SY | en_US |
dc.contributor.author | Li, CT | en_US |
dc.contributor.author | Hsieh, WF | en_US |
dc.date.accessioned | 2019-04-03T06:37:29Z | - |
dc.date.available | 2019-04-03T06:37:29Z | - |
dc.date.issued | 2004-05-01 | en_US |
dc.identifier.issn | 2469-9950 | en_US |
dc.identifier.uri | http://dx.doi.org/10.1103/PhysRevB.69.184104 | en_US |
dc.identifier.uri | http://hdl.handle.net/11536/26792 | - |
dc.description.abstract | Investigation of the structural and vibrational properties of the PbxCa1-xTiO3 (PCT) system exhibits two phase transitions in the range of x=0-1 by using x-ray powder diffraction and Raman spectroscopy. The first transition occurring at xsimilar to0.65 corresponds to the tetragonal-to-cubic phase and the second one occurs near x=0.35 is attributed to the orthorhombic-to-cubic phase. The absence of the intermediate tetragonal phase between orthorhombic and cubic phases (0<x<0.35) may be mostly attributed to the very restricted region in the PCT system. In addition, a decreasing giant LO-TO splitting behavior similar to that exhibited in PbxSr1-xTiO3 system for lower Pb concentration was also observed, which has been attributed to the highly Pb-O covalent bonding to reduce the long-range Coulomb interaction. Comparison of the change of line shapes of A(1)(1TO) mode among three PbTiO3-based perovskites indicates that the anharmonicity will become more conspicuous due to the larger high-order potential terms of Ba2+ and Ca2+ substitution than Sr2+ substitution for Pb2+. | en_US |
dc.language.iso | en_US | en_US |
dc.title | Lattice dynamics of perovskite PbxCa1-xTiO3 | en_US |
dc.type | Article | en_US |
dc.identifier.doi | 10.1103/PhysRevB.69.184104 | en_US |
dc.identifier.journal | PHYSICAL REVIEW B | en_US |
dc.citation.volume | 69 | en_US |
dc.citation.issue | 18 | en_US |
dc.citation.spage | 0 | en_US |
dc.citation.epage | 0 | en_US |
dc.contributor.department | 光電工程研究所 | zh_TW |
dc.contributor.department | Institute of EO Enginerring | en_US |
dc.identifier.wosnumber | WOS:000222095500025 | en_US |
dc.citation.woscount | 22 | en_US |
Appears in Collections: | Articles |
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