完整後設資料紀錄
DC 欄位語言
dc.contributor.authorKuo, SYen_US
dc.contributor.authorLiao, WYen_US
dc.contributor.authorHsieh, WFen_US
dc.date.accessioned2019-04-03T06:39:23Z-
dc.date.available2019-04-03T06:39:23Z-
dc.date.issued2001-12-01en_US
dc.identifier.issn1098-0121en_US
dc.identifier.urihttp://dx.doi.org/10.1103/PhysRevB.64.224103en_US
dc.identifier.urihttp://hdl.handle.net/11536/29203-
dc.description.abstractWe report Raman and x-ray diffraction studies of polycrystalline BaxSr1-xTiO3 (BST) prepared by the sol-gel technique in the range of x = 0 to 1.0. Other than a tetragonal to cubic phase transition at composition x approximate to0.75 of the BST powders detected by x-ray diffraction and Raman spectroscopy, a new structural ordering transition around x approximate to0.4-0.5 is observed due to the atomic arrangement. By taking the anharmonic coupling between the three A(1) (TO) modes into account, the observed repulsion of the giant LO-TO splitting is a result of decreasing cell dimension and strengthening the electron-phonon coupling. The results help us to explain the weakening of the ferroelectricity in the BST tetragonal phase as x decreases. The anomalous inconsistency in our experimental results and theoretical prediction are attributed to the lack of detailed information of dynamical effective charges in the BaxSr1-xTiO3 compounds.en_US
dc.language.isoen_USen_US
dc.titleStructural ordering transition and repulsion of the giant LO-TO splitting in polycrystalline BaSr1-xTiO3en_US
dc.typeArticleen_US
dc.identifier.doi10.1103/PhysRevB.64.224103en_US
dc.identifier.journalPHYSICAL REVIEW Ben_US
dc.citation.volume64en_US
dc.citation.issue22en_US
dc.citation.spage0en_US
dc.citation.epage0en_US
dc.contributor.department光電工程研究所zh_TW
dc.contributor.departmentInstitute of EO Enginerringen_US
dc.identifier.wosnumberWOS:000172733300018en_US
dc.citation.woscount60en_US
顯示於類別:期刊論文


文件中的檔案:

  1. 9b8f38201fcfec710834491a1eaad72e.pdf

若為 zip 檔案,請下載檔案解壓縮後,用瀏覽器開啟資料夾中的 index.html 瀏覽全文。