Dynamics of excited solvated electrons in aqueous solution monitored with femtosecond-time and polarization resolution

被引:83
作者
Assel, M [1 ]
Laenen, R [1 ]
Laubereau, A [1 ]
机构
[1] Tech Univ Munich, Dept Phys E11, D-85748 Garching, Germany
关键词
D O I
10.1021/jp972499y
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Transient pump-probe spectroscopy of equilibrated solvated electrons is carried out in aqueous NaCl solution (5.9 M) in the visible and near-infrared using pulses of 100-170 fs duration and polarization resolution. Excitation is performed by a pump pulse at 620 nm in the blue wing of the electronic absorption band. Transient bleaching occurs in a broad interval around the maximum of the e(-) absorption at 705 nm, accompanied by induced absorption at longer wavelengths. No hole-burning features are observed within our experimental time resolution suggesting a time constant tau(1) < 80 fs for rapid solvent relaxation and/or population redistribution among the excited electronic states. The relaxation dynamics involves a first intermediate, a frequency-shifted excited-state p' with Lifetime tau(2) = 190 +/- 40 fs. A further time constant tau(3) = 1.2 +/- 0.4 ps accounts for the recovery of the ground state. The latter process involves a second intermediate that is assigned as a modified ground-state s ". Evidence for stimulated emission suggests a distinct red shift of the transition p'-->ground state to 800 +/- 20 nm, while the transient absorption band of electrons in the s "-level is centered at 780 +/- 20 nm. The negligible anisotropy <0.01 of the probe absorption measured during and after the excitation process indicates that the observed distribution of solvent cavities of hydrated electrons is close to spherical symmetry.
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页码:2256 / 2262
页数:7
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