Femtosecond time-resolved energy transfer from CdSe nanoparticles to phthalocyanines

被引:51
作者
Dayal, S. [1 ]
Krolicki, R. [1 ]
Lou, Y. [1 ]
Qiu, X. [1 ]
Berlin, J. C. [1 ]
Kenney, M. E. [1 ]
Burda, C. [1 ]
机构
[1] Case Western Reserve Univ, Ctr Chem Dynam & Nanomat Res, Dept Chem, Cleveland, OH 44106 USA
来源
APPLIED PHYSICS B-LASERS AND OPTICS | 2006年 / 84卷 / 1-2期
关键词
ULTRAFAST CARRIER DYNAMICS; SEMICONDUCTOR QUANTUM DOTS; ELECTRON-TRANSFER; DEPENDENCE; APOPTOSIS; EXCITON;
D O I
10.1007/s00340-006-2293-z
中图分类号
O43 [光学];
学科分类号
070207 ; 0803 ;
摘要
The first real-time observation of the early events during energy transfer from a photoexcited CdSe nanoparticle to an attached phthalocyanine molecule are presented in terms of a femtosecond spectroscopic pump-probe study of the energy transfer in conjugates of CdSe nanoparticles (NPs) and silicon phthalocyanines (Pcs) with 120 fs time resolution. Four different silicon phthalocyanines have been conjugated to CdSe NPs. All of these have proven potential for photodynamic therapy (PDT). In such NP-Pc conjugates efficient energy transfer (ET) from CdSe NPs to Pcs occurs upon selective photoexcitation of the NP moiety. Spectral analysis as well as time-resolved fluorescence up-conversion measurements revealed the structure and dynamics of the investigated conjugates. Femtosecond transient differential absorption (TDA) spectroscopy was used for the investigation of the non-radiative carrier and ET dynamics. The formation of excitons, trapped carriers states, as well as stimulated emission was monitored in the TDA spectra and the corresponding lifetimes of these states were recorded. The time component for energy transfer was found to be between 15 and 35 ps. The ET efficiencies are found to be 20-70% for the four Pc conjugates, according to fluorescence quenching experiments. Moreover, as a result of the conjugation between NP and the Pcs the photoluminescence efficiency of the Pc moieties in the conjugates do not strictly follow the quantum yields of the bare phthalocyanines.
引用
收藏
页码:309 / 315
页数:7
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