激发态
波包
化学
分子物理学
吸收光谱法
人口
吸收(声学)
绝热过程
原子物理学
超快激光光谱学
激发
非绝热的
振动光谱学
啁啾声
物理
光谱学
光学
量子力学
社会学
人口学
激光器
作者
I. U. Goldschleger,V. Senekerimyan,M. S. Krage,H. Ye. Seferyan,Kenneth C. Janda,V. A. Apkarian
摘要
In both water and in ice, the absorption spectra of bromine are dramatically broadened and blueshifted, and all fluorescence is quenched. Time resolved, electronically resonant transient grating measurements are carried out to characterize the vibronic dynamics of the trapped molecule in its electronic B(3Pi0u) state in ice. Independent of the initial excitation energy, after the first half-period of motion, a vibrational packet is observed to oscillate near the bottom of the potential, near nu=1. The oscillations undergo a chirped decay to a terminal frequency of 169 cm(-1) on a time scale of taunu=1240 fs, to form the stationary nu=0 level. The electronic population in the B state decays in taue=1500 fs. Adiabatic following to the cage-compression coordinate is a plausible origin of the chirp. Analysis of the absorption spectrum is provided to recognize that solvent coordinates are directly excited in the process. The observed blueshift of the absorption is modeled by considering the Br2-OH2 complex. Two-dimensional simulations, that explicitly include the solvent coordinate, reproduce both the time data and the absorption spectrum. The observed sharp vibrational recursions can be explained by overdamped motion along the solvent coordinate, and wave packet focusing by fast dissipation during the first half-period of motion of the molecular coordinate.
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