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The inverse Raman effect is a form of Raman scattering first noted by W. J. Jones and Boris P. Stoicheff. In some circumstances, Stokes scattering can exceed anti-Stokes scattering; in these cases the continuum (on leaving the material) is observed to have an absorption line (a dip in intensity) at ν L +ν M.
The Raman effect should not be confused with emission (fluorescence or phosphorescence), where a molecule in an excited electronic state emits a photon and returns to the ground electronic state, in many cases to a vibrationally excited state on the ground electronic state potential energy surface. Raman scattering also contrasts with infrared ...
The SERS effect is so pronounced because the field enhancement occurs twice. First, the field enhancement magnifies the intensity of incident light, which will excite the Raman modes of the molecule being studied, therefore increasing the signal of the Raman scattering. The Raman signal is then further magnified by the surface due to the same ...
Stimulated Raman spectroscopy, also referred to as stimulated Raman scattering (SRS), is a form of spectroscopy employed in physics, chemistry, biology, and other fields. . The basic mechanism resembles that of spontaneous Raman spectroscopy: a pump photon, of the angular frequency , which is scattered by a molecule has some small probability of inducing some vibrational (or rotational ...
Like ordinary Raman spectroscopy, RRS observes vibrational transitions producing a nonzero change in the polarizability of the molecule or material being studied. Resonance Raman scattering differs from fluorescence in that it occurs without vibrational relaxation during the lifetime of the excited electronic state.
The Raman cross section for the vibration of the aromatic ring in toluene around 1000 cm −1 is on the order of 10 −29 cm 2 /molecule·steradian. Therefore, the Raman signal is around 26×10 −23 W/molecule·steradian or 3.3×10 −21 W/molecule (over 4π steradians). That is 0.014 photon/sec·molecule.
It states that no normal modes can be both Infrared and Raman active in a molecule that possesses a center of symmetry. This is a powerful application of group theory to vibrational spectroscopy, and allows one to easily detect the presence of this symmetry element by comparison of the IR and Raman spectra generated by the same molecule. [1]
[88] [89] Use of the English versions, "Raman effect" and "Raman lines" immediately followed. [90] [22] [91] In addition to being a new phenomenon itself, the Raman effect was one of the earliest proofs of the quantum nature of light. Robert W. Wood at the Johns Hopkins University was the first American to confirm the Raman effect in the early ...