Page 500 - Fiber Optic Communications Fund
P. 500

Nonlinear Effects in Fibers                                                        481




                                           P (0)= 10 P s (0) (dBm)∕10  mW
                                            s
                                                = 0.1 mW,                                 (10.419)
                                                 1 − exp (− L)
                                                          p
                                          L eff,p  =
                                                       p
                                                 1 − exp (−0.08 × 2)
                                               =
                                                    0.08 × 10 −3
                                               = 1.848 km,                                (10.420)
                                g P (0)L eff,p  1 × 10 −13  × 100 × 10 −3  × 1.848 × 10 3
                                 R p
                                           =
                                    A                   40 × 10 −12
                                     eff
                                           = 0.462,                                       (10.421)
                                                  L = 0.092.                            (10.422)
                                                  s
           So, the gain dominates the loss. From Eq. (10.413), we find
                                            P (L)= P (0)e −0.092+0.462
                                             s     s
                                                = 0.1447 mW.                              (10.423)



           10.11.1  Time Domain Description
           In the time domain, stimulated Raman scattering can be explained as follows [81]. When a high-intensity
           optical pulse interacts with a molecule, it perturbs the electronic structure of the molecule and results in
           intensity-dependent polarizability of the molecule (see Section 10.2). This electronic effect occurs on a time
           scale shorter than the pulse width of the optical pulse, and it can be considered instantaneous. However,
           perturbation of the electronic structure by the optical pulse also perturbs the Coloumb interaction between the
           nuclei and the electronic structure, which can excite molecular vibrations. These vibrations, in turn, perturb the
           electronic structure, leading to a delayed change in polarizability. The time- and intensity-dependent change
           in polarizability (or equivalent refractive index) associated with the excitation of a molecular vibration is the
           Raman effect, whereas the instantaneous intensity-dependent change in polarizability is the Kerr effect.
                                                                                 2
            As mentioned in Section 10.4, the Kerr effect is taken into account by the term |q| q in the nonlinear
           Schrödinger equation. In the presence of the Raman effect, it can be modified as [82]
                                                             ∞
                                    2                2                      2
                            |q(T, Z)| → (1 − )|q(T, Z)| +   h(s)|q(T − s, Z)| ds,  (10.424)
                                                           ∫
                                                            −∞
           where  is the fraction of the nonlinearity resulting from the Raman contributions and h(T) is the normalized
           Raman response function, with
                                                 ∞
                                                   h(T)dT = 1                             (10.425)
                                               ∫
                                                −∞
           and h(−|t|)= 0 to ensure causality. The response function h(T) is specific to the medium and the imaginary
           part of its Fourier transform is related to the Raman gain coefficient g(Ω) [81, 83].Let
                                                             2
                                             P(T, Z)= |q(T, Z)| ,                         (10.426)
                                                                2
                                          P(T − s, Z)= |q(T − s, Z)| .                    (10.427)
   495   496   497   498   499   500   501   502   503   504   505