Page 299 - Tunable Lasers Handbook
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6 Transition Metal Solid-state  Lasers   259

                     only one d electron, to first-order approximation. there are only two levels. In a
                     strict sense, a two-level laser would not lase since a population inversion could
                     not  be  achieved. However. because  the  Ti:AI,O,  laser operates  on  a  vibronic
                     transition. it can operate much like a four-level laser. In addition. an extremely
                     wide tuning range is available with this material. Full  width at half-maximum
                     (FWHM)  spectral bandwidth is roughly  one-third of  the peak  emission ~ave-
                     length.  Such  a  wide  spectral  bandwidth  gives  this  laser  material  one  of  the
                     widest tuning ranges of any laser.
                        Many of the desirable properties of Ti:A1,0,  result from the single electron
                     in the 3d level. Since there is only one electron available. the mutual repulsion
                     effects  are  zero.  Consequently.  only  the  spin  orbit  and  crystal  field  effects
                     remain. Crystal field effects split the degenerate levels associated with the cen-
                     tral field approximation into two levels. With only two levels, deleterious excited
                     state absorption is negligible. Crystal field effects are the same as those associ-
                     ated with the Cr:A1,03, namely. a strong octahedral field with a tr-iginol distor-
                     tion. Since there is only a single 3d electron, rather than the three 3d electrons
                     associated with Cr, the levels are labeled differently. Neglecting the triginol dis-
                     tortion, the triply degenerate ground level is labeled as T, and the doubly degen-
                     erate  esciied  state  is  labeled  as  'E. Triginol  distortioil further  splits  the  T,
                     grmnd level into two relatively closely spaced levels and the spin orbif  interac-
                     tion further splits the lower of these into two levels [27],
                        Ti:A1,0;  is produced by replacing a small fraction of the A1 atoms with Ti
                     atoms. Concentrations of Ti are relatively low, often less than 0.0015 by weight.
                     Although higher concentrations are possible, considerations such as optical qual-
                     ity tend to limit the Ti concentration. Ti sees the same symmetry as the A1 atoms
                     in A1,O;.
                        Since only a small fraction of the A1 is replaced with either Cr for Cr:AI,03
                     or Ti  for Ti:AI,O,,  the optical and mechanical properties of  Ti:AI,O,  are very
                     nearly the same as Cr:AI,O,.  However, addition of Ti tends to produce a harder
                     crystal than undoped 41,O,.
                        Ti:Al,03  displays polarization-dependent absorption bands that peak about
                     0.49 pm, Absorption of radiation polarized along the optic axis, x polarized, is
                     more than twice as strong as absorption of  radiation polarized perpendicular to
                     the optic axis, o polarized [28]. For both polarizations, a shoulder in the absorp-
                     tion spectra appears at about 0.51 ym.  Because absorption occurs from wave-
                     lengths shorter than 0.45 pan  to wavelengths longer than 0.60 pm, a wide range
                     of pump wavelengths is possible. However. even with relatively lorn Ti concen-
                     trations, peak absorption coefficients on the order of 200 m-1  are common.
                        Quantum efficiency can be deduced from the measurement of the lifetime of
                     the upper laser level as a function of temperature. At cryogenic temperatures, the
                     upper laser level lifetime has been measured to be 3.87 ys [29]. Lifetime is nom-
                     inally independent of temperature to about 200 K. At room temperature the life-
                     time is nominally 3.2 ps and it decreases rapidly as the temperature decreases.
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