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dc.contributor.authorLuo, C. W.en_US
dc.contributor.authorCheng, P. C.en_US
dc.contributor.authorTu, C. M.en_US
dc.contributor.authorKuo, C. N.en_US
dc.contributor.authorWang, C. M.en_US
dc.contributor.authorLue, C. S.en_US
dc.date.accessioned2019-04-03T06:40:07Z-
dc.date.available2019-04-03T06:40:07Z-
dc.date.issued2016-07-26en_US
dc.identifier.issn1367-2630en_US
dc.identifier.urihttp://dx.doi.org/10.1088/1367-2630/18/7/073045en_US
dc.identifier.urihttp://hdl.handle.net/11536/134130-
dc.description.abstractWe report a study of ultrafast dynamics of photoexcited electrons and phonons in Sr3Ir4Sn13 using dual-color transient reflectivity change (Delta R/R) measurements. Time resolved optical spectroscopy of collective excitations reveal the marked features near its structural phase transition temperature T* similar or equal to 147 K. Two distinctive oscillatory timescales in Delta R/R have been clearly resolved. The rapid THz-range oscillations are attributed to the dynamics of the optical phonons which strongly correlate to the structural phase transition. The slow GHz-range oscillatory phenomenon which only occurs below about 150 K is associated with the dynamic response of the longitudinal-acoustic phonons. These low-energy phonons show a softening feature on approaching the transition temperature, also indicating a strong relevance to the structural phase transition. The information that we demonstrated would provide a deeper understanding of the structural phase transition in Sr3Ir4Sn13.en_US
dc.language.isoen_USen_US
dc.subjectSr3Ir4Sn13en_US
dc.subjectphononen_US
dc.subjecttime resolved optical spectroscopyen_US
dc.titleDynamics of phonons in Sr3Ir4Sn13: an experimental study by ultrafast spectroscopy measurementsen_US
dc.typeArticleen_US
dc.identifier.doi10.1088/1367-2630/18/7/073045en_US
dc.identifier.journalNEW JOURNAL OF PHYSICSen_US
dc.citation.volume18en_US
dc.citation.spage0en_US
dc.citation.epage0en_US
dc.contributor.department電子物理學系zh_TW
dc.contributor.departmentDepartment of Electrophysicsen_US
dc.identifier.wosnumberWOS:000381880800001en_US
dc.citation.woscount5en_US
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