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Proceedings of SPIE, the International Society for Optical Engineering/Proceedings of SPIE

Picosecond vibrational photon echo experiments in liquids and glasses

David A. Zimdars, Andrei Tokmakoff, Beate Sauter, Scott Chen, Alfred S. Kwok, M. D. Fayer

Published Jul 27, 1994• 0 citations
Publisher

Abstract

An account is given of the first infrared vibrational photon echo experiments conducted in liquids and a glasses. The experiments were performed on the CO stretching mode of the solute tungsten hexacarbonyl (W(CO)6) at approximately 5.05 micrometers (approximately 1980 cm-1) in the solvents 2-methytetrahydrofuran, and 2-methylpentane (2-MP). In 2-MP, it was possible to observe the photon echo decay at room temperature and follow the temperature dependence from room temperature to 10 K. The photon echo experiments were conducted using the Stanford superconducting-linear-accelerator-pumped Free Electron Laser as the source of tunable ps infrared pulses.

DOI
10.1117/12.181368

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An account is given of the first infrared vibrational photon echo experiments conducted in liquids and a glasses. The experiments were performed on the CO stretching mode of the solute tungsten hexacarbonyl (W(CO)6) at approximately 5.05 micrometers (approximately 1980 cm-1) in the solvents 2-methytetrahydrofuran, and 2-methylpentane (2-MP). In 2-MP, it was possible to observe the photon echo decay at room temperature and follow the temperature dependence from room temperature to 10 K. The photon echo experiments were conducted using the Stanford superconducting-linear-accelerator-pumped Free Electron Laser as the source of tunable ps infrared pulses.
The first infrared vibrational photon echo experiments conducted in a liquid and a glass are reported. The experiments were performed on the CO stretching mode of tungsten hexacarbonyl at 5.1 micrometers (1960 cm-1) in 2-methyltetrahydrofuran over the temperature range 300 K to 16 K using picosecond pulses from the free electron laser at Stanford University. In addition, the first vibrational population relaxation measurements spanning a temperature range that takes a system from a liquid to a supercooled liquid to a glass are reported.
The first infrared vibrational photon echo experiments conducted in a liquid and a glass are reported. The experiments were performed on the CO stretching mode of tungsten hexacarbonyl at 5.1 \ensuremath{\mu}m (1960 ${\mathrm{cm}}^{\mathrm{\ensuremath{-}}1}$) in 2-methyltetrahydrofuran over the temperature range 300 to 16 K using picosecond pulses from the free electron laser at Stanford University. In addition, the first vibrational population relaxation measurements spanning a temperature range that takes a system from a liquid to a supercooled liquid to a glass are reported.
A superconducting accelerator-pumped free-electron laser (SCA/FEL) is used to perform photon echo experiments on a near-IR dye molecule in a polymeric glass. The SCA/FEL produces Fourier-transform-limited picosecond pulses at a repetition rate of 11.8 MHz. Its wavelength is continuously tunable. The experiments are conducted at 0.776 μm by doubling the output of the SCA/FEL tuned to 1.55 μm. At this wavelength, the SCA/FEL is operated in a burst mode. The duration of the bursts (macropulses) is 2 ms with a repetition rate of 10 Hz. Each individual pulse (micropulse) has a length of 3.2 ps and is approximately 1 μJ in energy. In the experiment a number of single micropulses are selected from each macropulse. The doubling, stabilization, synchronization, single-pulse selection, and detection electronics are described. These are the first photon echo experiments and, to our knowledge, the first optical coherence experiments performed using a free-electron laser as a source.
Vibrational photon echo experiments were performed on the asymmetric CO stretching mode of tungsten hexacarbonyl in glassy dibutylphthalate as a function of temperature using sub-picosecond infrared pulses (1976 cm−1) from a free electron laser. The echo decays display pronounced beats and are bi-exponential. The beats and bi-exponential decays arise because the bandwith of the pulses exceed the vibrational anharmonicity, leading to the excitation and dephasing of a multilevel coherence. From the beat frequency, the anharmonicity is determined to be 14.7 cm−1. From the bi-exponential decay components, the temperature-dependent vibrational dephasing of both the v = 0 → 1 and v = 1 → 2 transitions are determined.
We present the first infrared photon echo study of liquid water. For the O-H stretch vibration of HDO in D2O{\mathrm{D}}_{2}\mathrm{O}D2​O, femtosecond four-wave mixing experiments reveal an extraordinary short pure dephasing time T2∗{T}_{2}^{*}T2∗​ on the order of 90 fs. This unusually fast time scale of dephasing is rationalized by taking into account the large anharmonicity of the hydrogen bonded O-H stretching mode.