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Nonlinear Effects in Fibers                                                        479



                      Virtual energy
                         state


                                                        ħω p           Ω = ω – ω = ω – ω p
                                                                                 a
                                                                              s
                                                                           p
                                       ħω p    ħω s             ħω a


                                                                            Vibrational
                                                                              state
                                ħΩ


                                       Stokes Raman    Anti-Stokes Raman
                                        Scattering        Scattering

                                 Figure 10.32  Stokes and anti-Stokes Raman scattering.



           independently by Landsberg and Manderlstam [78]) in 1928. The molecules in the medium have several
           vibrational states (or phonon modes). When a light wave (photons) interacts with sound waves (phonons), the
           frequency of the light wave is shifted up or down. The shift in frequency gives information about the phonon
           modes of the molecules. When the scattered photon has a frequency lower than the incident photon, it is
           known as Stokes shift. Stokes Raman scattering can be described quantum mechanically as the annihilation
           of a pump photon of energy ℏ and the creation of a Stokes photon of lower energy ℏ , and absorption
                                                                                   s
                                    p
           of the energy ℏ( −  ) by the molecules by making transition from a low-energy vibrational state to a
                              s
                         p
           high-energy vibrational state (see Fig. 10.32). A lower-energy photon has lower frequency and, therefore,
           Stokes Raman scattering leads to a red shift of the incident light wave. If the molecule makes transition from
           a high-energy vibrational state to a low-energy vibrational state in the presence of an incident pump of energy
           ℏ , the difference in energy is added to the incident photon, leading to a photon of higher energy ℏ (which
             p
                                                                                          a
           is of higher frequency). This is known as anti-Stokes Raman scattering. Raman scattering is quite useful in
           chemistry, since vibrational information is specific to the chemical bonds and symmetry of molecules.
            Spontaneous Raman scattering is typically very weak. In 1962, it was found that an intense-pump optical
           wave can excite molecular vibrations and, thereby, stimulate molecules to emit photons of reduced energy
           (a Stokes wave), to which most of the pump energy is transferred [79]. This is known as stimulated Raman
           scattering. The interaction between the pump and the Stokes wave is described by the following coupled
           equations under CW conditions [80]:
                                             d
                                               s
                                                 = g   −   ,                         (10.406)
                                                            s s
                                                    R p s
                                             dZ
                                           d     
                                             p     p
                                               =−    g   −   ,                       (10.407)
                                                      R p s
                                                              p p
                                           dZ     
                                                    s
           where  and  are the optical intensities of the pump and the Stokes waves, respectively,  and  are the
                 p     s                                                            p     s
           fiber loss coefficients at the pump and the Stokes frequencies, respectively, and g (Ω), Ω=  −  is the
                                                                             R         p   s
           Raman gain coefficient. The amplification of the Stokes wave by the pump wave can be understood from
           Eqs. (10.406) and (10.407). To simplify the analysis, we assume that the pump intensity is much larger than
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