Abstract

The dynamics of molecular solvation at the air/water interface has been monitored with femtosecond time-resolved pump-sum frequency generation (TR-SFG), a technique that has been shown to be feasible in the study of ultrafast rotional motions. In the work reported here, the solvation process was monitored by femtosecond photoexcitation of interfacial coumarin 314 (C314) molecules. In these experiments, the SFG signal is brought into a vibrational resonance with the carbonyl symmetric stretch of C314 by tuning the IR pulse to the carbonyl frequency by using a pump-TR-SFG probe. Two solvation time constants were obtained, 230 ± 40 fs and 2.17 ± 0.3 ps. These results are the same within experimental error as those measured in time-resolved second-harmonic generation (TR-SHG) experiments. This suggests that the solvent response is due to solvation-induced shifts of the electronic-state energies in the SFG hyperpolarizability and not significantly to solvation effects on the energy of the carbonyl vibration no...

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