Femtosecond excitation dynamics in gold nanospheres and nanorods

被引:90
作者
Varnavski, OP [1 ]
Goodson, T
Mohamed, MB
El-Sayed, MA
机构
[1] Univ Michigan, Dept Chem, Ann Arbor, MI 48109 USA
[2] Georgia Inst Technol, Sch Chem & Biochem, Laser Dynam Lab, Atlanta, GA 30332 USA
关键词
D O I
10.1103/PhysRevB.72.235405
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Femtosecond visible photoluminescence is detected from gold nanoparticles using time-resolved fluorescence upconversion spectroscopy. We directly compared this fast luminescence from gold nanospheres (subset of 25 nm) with that obtained from nanorods (subset of 15x40 nm, subset of 15x27 nm) under vis (3.02 eV) and UV(4.65 eV) excitation. A fast (similar to 50 fs) decay was obtained for the nanoparticles and the emission was depolarized. Degenerate femtosecond pump-probe experiments in the low excitation intensity regime demonstrated much slower electron thermalization and/or equilibration dynamics on the time scale of a few hundred femtoseconds. These features strongly indicate a d-hole-conduction electron recombination process as the origin of this photoluminescence. A direct comparison of the fast emission spectra from nanorods and nanospheres is used to discuss the emission enhancement mechanism. These results suggest that the classical local field enhancement theory describes quantitatively well many of the emission features of nanorods with respect to those for nanospheres without invoking more complex models.
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页数:9
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