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dc.contributor.authorSun, K. W.en_US
dc.contributor.authorKechiantz, A.en_US
dc.date.accessioned2014-12-08T15:16:11Z-
dc.date.available2014-12-08T15:16:11Z-
dc.date.issued2006-07-15en_US
dc.identifier.issn0022-3093en_US
dc.identifier.urihttp://dx.doi.org/10.1016/j.jnoncrysol.2006.03.015en_US
dc.identifier.urihttp://hdl.handle.net/11536/12022-
dc.description.abstractWe report theoretical and experimental results of our investigation on carrier capture and relaxation processes in undoped and modulation-doped InAs/GaAs self-assembled quantum dots (QDs). We find that carrier capture and relaxation in the ground state is faster in the modulation-doped quantum dots compared to the case in neutral dots at an excitation level as low as one electron-hole pair per dot. The ultrafast photoluminescence (PL) transient rise time observed in the charged dots is attributed to the relaxing of strained field induced by the presence of cold carriers in the dots. The Hamiltonian of electron's interaction with local vibrating field and carrier capture time are also calculated. (c) 2006 Elsevier B.V. All rights reserved.en_US
dc.language.isoen_USen_US
dc.subjectlaser-matter interactionsen_US
dc.subjectoptical spectroscopyen_US
dc.subjectquantum wellsen_US
dc.subjectwires and dotsen_US
dc.subjectluminescenceen_US
dc.subjectultrafast processes and measurementsen_US
dc.subjectupconversionen_US
dc.subjecttime resolved measurementsen_US
dc.titleUltrafast carrier capture in charged InAs quantum dotsen_US
dc.typeArticle; Proceedings Paperen_US
dc.identifier.doi10.1016/j.jnoncrysol.2006.03.015en_US
dc.identifier.journalJOURNAL OF NON-CRYSTALLINE SOLIDSen_US
dc.citation.volume352en_US
dc.citation.issue23-25en_US
dc.citation.spage2355en_US
dc.citation.epage2359en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.department應用化學系分子科學碩博班zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.contributor.departmentInstitute of Molecular scienceen_US
dc.identifier.wosnumberWOS:000239110200016-
Appears in Collections:Conferences Paper


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