Probing the strength of the system-bath interaction by three-pulse photon echoes

被引:8
作者
Christensson, N. [1 ]
Dietzek, B. [1 ,2 ]
Yartsev, A. [1 ]
Pullerits, T. [1 ]
机构
[1] Lund Univ, Dept Chem Phys, SE-22100 Lund, Sweden
[2] Univ Jena, Inst Phys Chem, D-07743 Jena, Germany
关键词
dyes; high-speed optical techniques; photon echo; reaction kinetics; solvation; solvent effects; DOMAIN RESONANT SPECTROSCOPIES; POLAR SOLVATION DYNAMICS; PEAK SHIFT; INTRAMOLECULAR VIBRATIONS; 3RD-ORDER; SPECTRA; TEMPERATURE; PROPAGATION; LIQUIDS; ENERGY;
D O I
10.1063/1.2990652
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
We explore how the width of the three-pulse photon echo signal at long population times can be used to determine the strength of the system-bath interaction. Using simulation with finite pulses we show that a simple relation exist between the width of the echo signal, the coupling strength, and the pulse autocorrelation. The derived model is applied to Rhodamine 6G in alcoholic solution, a paradigm system for the study of solvation dynamics, and the results are compared to conventional methods. The independently determined coupling strength forms the basis for a computationally inexpensive route to determine the entire spectral density, the key parameter when considering system-bath interactions. Our method allows us to accurately estimate the relative amplitude of fast and slow components in the correlation function using only impulsive limit simulations. We show that the peak shift significantly overestimates the amplitude of the fastest decay component for our experimental data. Changing solvent from methanol to 1-hexanol we observe a narrowing of the width of the echo profile. The changes in the echo width allow us to estimate the changes of the coupling strength in various solvents.
引用
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页数:7
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