Abstract
Infrared (IR)-induced two-photon absorption (TPA) in synthesized PbO–Ga2O3–Bi2O3–CdO (PGBC) glasses doped by Eu3+ and Tm3+ rare earth (RE3+) ions was investigated. Temperature-dependent measurements of TPA were carried out in the mid-IR spectral range. A CO pulsed laser (λ = 5.5 μm, energy power density up to 3.8 GW/cm2 per pulse with picosecond pulse duration) was applied as the source of photoinducing IR radiation. An optical parametrical generator cut from a proustite crystal was used as the source of the fundamental TPA beam within the 3–7.5 μm spectral range. Absolute values of the TPA coefficients were more than 13% higher than corresponding values obtained for other similar glasses (As2Te3–CaCl2–PbCl2 [1] or Sb2Se3–BaCl2–PbCl2 [2]). The PGBC system investigated possessed a shorter time response (about 12 ps) compared with other IR nonlinear optical glasses. It was also established that all nonlinear optical susceptibilities were dependent on the type of RE3+ ion. A maximum value of the TPA was achieved for the glasses doped by Tm3+. The TPA values increased significantly below 45 K. Ab initio molecular dynamics and quantum chemical simulations were performed in order to evaluate the possible role of electron–phonon anharmonic interactions in the observed phenomena. The influence of the external CO photoinduced pump beam through the photoinduced electrostricted anharmonic electron–phonon interactions was simulated. A decrease of picosecond delaying time response compared with other glasses was achieved. To obtain independent confirmation of the observed dependencies, measurements were carried out of χxxxx(E) during the external IR pumping. The measured and theoretically calculated dependencies of the third-order susceptibilities were also compared. (© 2003 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim)
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