Raman scattering, high-frequency

The metal substrate evidently affords a huge ( 10 and even as high as 10 [84, 85]) increase in the cross-section for Raman scattering of the adsorbate. There are two broad classes of mechanisms which are said to contribute to this enhancenient [, and Ml- The first is based on electromagnetic effects and the second on cheniicaT effects. Of these two classes the fomier is better understood and, for the most part, the specific mechanisms are agreed upon the latter is more complicated and is less well understood. SERS enhancenient can take place in either physisorbed or chemisorbed situations, with the chemisorbed case typically characterized by larger Raman frequency shifts from the bulk phase. 

Ulness D J, Stimson M J, Kirkwood J C and Albrecht A C 1997 Interferometric downconversion of high frequency molecular vibrations with time-frequency-resolved coherent Raman scattering using quasi-cw noisy laser light C-H stretching modes of chloroform and benzene J. Rhys. Chem. A 101 4587-91... 

Since Raman scattered light intensity is very weak, of the order of 10-7 of the excitation line intensity, more powerful laser sources than the He-Ne laser are often needed. The Ar+ laser emits various lines in the region from 457.9 nm to 514.5 nm, of which the most powerful lines (typically — 700 mW) at 488.0 nm (blue) and 514.5 nm (green) are preferred. Furthermore, two other factors which favor the use of the high frequency excitation lines are the peak sensitivity of the photomultipliers in this blue-green region (Fig. 8) and the fourth power Raman intensity law... 

Raman excitation. and I2s are the high-frequency and low-frequency components of the pump light pulse. A probe pulse of frequency 12 interacts with the coherence to present the optical response of the fundamental frequency 12 + C0fsl2. (c) Fourth-order coherent Raman scattering, the optical response of the second harmonic frequency 212 + co 2I2 is modulated by the vibrational coherence. 

A strong point of Raman spectroscopy for research in catalysis is that the technique is highly suitable for in situ studies. The spectra of adsorbed species interfere weakly with signals from the gas phase, enabling studies under reaction conditions to be performed. A second advantage is that typical supports such as silica and alumina are weak Raman scatterers, with the consequence that adsorbed species can be measured at frequencies as low as 50 cm-1. This makes Raman... 

I. Is it possible to observe a shift in coherent Raman scattering in the three-level system with A-type coupling We have done an experiment to obtain a femtosecond Raman gain spectrum in polydiacetylenes. The Raman spectrum is shifted to the red under increased pump (to i) intensity. By changing o>2> the amplification peak signal is to be shifted to lower frequency. If the optical Stark effect is observed, then, in principle, it should be possible to observe the effect of a high field on the coherent Raman spectrum (see Fig. 1). 

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