Ultrafast dynamics of lattice relaxation of excitons in quasi-one-dimensional halogen-bridged platinum complexes
Ultrafast dynamics of lattice relaxation of excitons in quasi-one-dimensional halogen-bridged platinum complexes
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DOI:
10.1103/physrevb.66.155112
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发表时间:
2002-10-15
影响因子:
3.7
通讯作者:
Kurita, S
中科院分区:
文献类型:
--
作者:
Tomimoto, S;Saito, S;Kurita, S
The temporal evolution of the photoexcited state in quasi-one-dimensional (1D) halogen-bridged platinum complexes [Pt(en)(2)][Pt(en)(2)X-2](ClO4)(4) (abbreviated as Pt-X, X=Cl, Br or I), has been comprehensively studied by femtosecond time-resolved luminescence spectroscopy. In Pt-Cl, new short-lived hot luminescence is found in the low-energy side of a self-trapped exciton (STE) luminescence band. The overall behavior of the STE luminescence band within 2 ps is well explained by the vibrational relaxation of the STE. The behavior is reproduced by a model calculation based on wave packet propagation on an interaction mode composed of frequency-dispersed bulk phonons. This model is also applied to the previous results in Pt-Br. For both Pt-Cl and Pt-Br, the frequency spectra of phonons which compose the interaction mode have been estimated. In Pt-I, the STE luminescence decays much faster than those in Pt-Cl and Pt-Br, showing existence of more effective nonradiative decay channel.