完整後設資料紀錄
DC 欄位語言
dc.contributor.authorWang, Yingen_US
dc.contributor.authorKobayashi, Takayoshien_US
dc.date.accessioned2014-12-08T15:07:16Z-
dc.date.available2014-12-08T15:07:16Z-
dc.date.issued2010-03-05en_US
dc.identifier.issn1439-4235en_US
dc.identifier.urihttp://dx.doi.org/10.1002/cphc.200900784en_US
dc.identifier.urihttp://hdl.handle.net/11536/5731-
dc.description.abstractWe report the relaxation times of electronic and vibrational coherence in the cyanine dye 1,1',3,3,3',3'-hexamethyl-4,4',5,5'-dibenzo-2,2'-indotricarbocyanine, measured using a 7.1 fs pulsed laser. The vibrational phase relaxation times are found to be between 380 and 680 fs in the ground and lowest excited singlet states. The vibrational dephasing times of the 294, 446, and 736 cm(-1) modes are relatively long among the six modes associated with excited-state wave packets. The slower relaxations are explained in terms of a coupled triplet of vibrational modes, which preserves coherence by forming a tightly bound group to satisfy the condition of circa conservation of vibrational energy. Using data from the negative-time range (i.e., when the probe pulse precedes the pump pulse), the electronic phase relaxation time is found to be 31 +/- 1 fs. The dynamic vibrational mode in the excited state (1171 cm(-1)), detected in the positive-time range, is also studied from the negative-time traces under the same experimental conditions.en_US
dc.language.isoen_USen_US
dc.subjectcyaninesen_US
dc.subjectfemtochemistryen_US
dc.subjectmode couplingen_US
dc.subjectrelaxation timesen_US
dc.subjecttime-resolved spectroscopyen_US
dc.titleElectronic and Vibrational Coherence Dynamics in a Cyanine Dye Studied Using a Few-Cycle Pulsed Laseren_US
dc.typeArticleen_US
dc.identifier.doi10.1002/cphc.200900784en_US
dc.identifier.journalCHEMPHYSCHEMen_US
dc.citation.volume11en_US
dc.citation.issue4en_US
dc.citation.spage889en_US
dc.citation.epage896en_US
dc.contributor.department電子物理學系zh_TW
dc.contributor.departmentDepartment of Electrophysicsen_US
dc.identifier.wosnumberWOS:000276062600022-
dc.citation.woscount4-
顯示於類別:期刊論文