Page 79 - High Power Laser Handbook
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Chemical Lasers     49


                      Figure 3.3
                      Diatomic molecule
                      motions that
                      determine energy
                      levels.







                                        x                            y


                              The partition function Z is approximately proportional to the
                             temperature T and has a weak dependence on the vibrational
                             level v, because B  is also weakly dependent on v. When las-
                                           J
                             ing, although deviations from this simple distribution can be
                             taken  into  account  in  advanced  models,  the  general  trend
                             remains.
                          3.  Vibrational  motion:  Classically,  vibrational  motion  can  be
                             viewed as a simple harmonic motion springlike mode. Quan-
                             tum mechanically, it is characterized as a simple harmonic
                             oscillator  that  sometimes  includes  anharmonic  terms.  The
                             associated energy levels are simply:

                                             ω(v + 1/2)                     (3.4)

                              where ω is vibrational quantum energy and v is vibrational
                             quantum number.

                         In contrast to translational and rotational degrees of freedom, vir-
                      tually all molecules are in the vibrational ground state (v = 0) in the
                      absence of chemical pumping. When pumping or lasing is occurring,
                      the  assumption  of  a  simple  thermal  behavior  correlated  with  the
                      translational temperature is invalid.
                         The rotational and vibrational energy level expressions were sim-
                      plified and do not include the higher-order terms necessary to accu-
                      rately  determine  energy  levels.  Equation  (3.5)  is  a  more  accurate
                      expression:

                        E(v, J) = ω(v + 1/2) + X(v + 1/2)  + B  × J × ( J + 1)
                                                   2
                                                      J
                               + B (v + 1/2) × J × ( J + 1) + higher-order terms   (3.5)
                                  1J
                      Typical values for HF and DF in the energy unit wave number are
                      shown in Table 3.2.



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