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BGO single crystals doped with Er3+, Tm3+ and Ho3+ rare-earth ions were prepared in the form of rod-type crystal fibers via the micro-pulling down technique to perform an extensive investigation of their visible, near- and mid-infrared luminescence properties and to really decide on their interest as solid-state laser media in the various spectral domains. Revisiting and completing the absorption spectra already available in the literature led to the derivation of more reliable "effective" radiative lifetimes and branching ratios. Registration of the fluorescence decays of the most important emitting levels versus dopant concentrations led for the first time to an unambiguous determination of "intrinsic" emission lifetimes – corresponding to negligible contributions from inter-ionic energy-transfers - and non-radiative multiphonon relaxation rates. Such data also allowed for the determination of the dominant phonon energy which comes into play in the electron-phonon coupling responsible for these multiphonon relaxation processes and for its lattice vibration origin, i.e. a high phonon energy of the order of 820 cm−1 corresponding to the coupling between bending vibrations of (GeO 4)4- tetrahedra and vibrations corresponding to motions of these (GeO 4)4- tetrahedra against the Bi3+ ions for which the rare-earth dopant ions substitute. Using the above data and different methods for the calibration of the registered emission spectra in cross section unit and for the derivation of gain cross section curves finally show that mid-infrared emissions of Er:BGO, Tm:BGO and Ho:BGO around 1.55 μm, 1.9 μm and 2 μm, respectively, occur with comparable gain cross sections as in the most important reference mid-infrared laser materials, although over slightly shifted thus complementary spectral domains. It is shown that potentialities also exist with Tm:BGO in the blue, deep-red and near-infrared spectral domains around 470 nm, 800 nm and 1.45 μm, by pumping the crystals with conventional pump sources and using some suitable co-dopants to avoid detrimental self-terminating processes. • Bi 4 Ge 3 O 12 rod-type crystal fibers doped with Er3+, Tm3+ and Ho3+ ions are successfully grown by using the micro-pulling down technique. • An extensive spectroscopic investigation is performed from the near-UV to the mid-infrared. • Effective radiative and intrinsic emission lifetimes are unambiguously determined for all the important emitting levels. • The origin and the energy of the phonons responsible for the non-radiative multiphonon relaxation of the emitting levels are clearly identified. • Emission and gain cross section spectra show the interest of Er3+, Tm3+ and Ho3+ doped BGO crystals for the high power mid-infrared laser application. [ABSTRACT FROM AUTHOR]

In this paper, the Floating zone technique was used to grow high-quality Cr3+:YScO 3 crystals. The absorption cross-sections of the 4A 2 →4T 1 transition and 4A 2 →4T 2 transitions were calculated to be 1.71 × 10−20 cm2 at 488 nm and 0.72 × 10−20 cm2 at 666 nm, respectively. The crystal field strength Dq, Racah parameters B, and C were calculated to be 1502 cm−1, 533 cm−1, and 3362 cm−1, respectively. In the Cr3+:YScO 3 crystal, the effective phonon energy and Huang-Rhys factor S were calculated to be 284 cm−1 and 8.62, respectively. The emission cross-section at 988 nm corresponding to the 4T 2 →4A 2 transition was calculated to be 1.44 × 10−20 cm2 with full width at half maximum (FWHM) of 318 nm. All the results show that Cr3+:YScO 3 crystal has the potential to be a tunable and ultrafast laser crystal. • Cr:YScO 3 crystals were successfully grown by the Floating zone technique(FZ) method. • Broad emission spectrum with full width at half maximum (FWHM) of 318 nm in Cr:YScO 3 crystals was observed. • Spectral properties and crystal field parameters of Cr:YScO 3 crystals were investigated and analysed. [ABSTRACT FROM AUTHOR]

Pr 3+ -doped YAlO 3 (YAP) single crystal was successfully grown by the Czochralski (Cz) method. Polarized absorption and polarized fluorescence spectra were measured at the room temperature. The spectroscopic parameters based on the polarized absorption spectra were calculated by Judd-Ofelt (J-O) theory for the first time. The fluorescence lifetime of 3 P 0 energy level was fitted to be 19.16 μs with the quantum efficiency of 95.8%. Through the analyzing of the spectroscopic properties, Pr:YAP crystal was demonstrated to be a promising candidate for solid state laser operation. [ABSTRACT FROM AUTHOR]

LaMgAl 11 O 19 (LMA) crystal with nominal Sm3+ concentrations of 8 at.% was grown by the Czochralski method. Polarized absorption spectra, polarized emission spectra and fluorescence decay curve of Sm:LMA crystal were recorded at room temperature. The absorption cross-sections at 404 nm were calculated to be 2.33 × 10−20 cm2 and 0.86 × 10−20 cm2 for σ and π polarization, respectively. The spontaneous transition rates, branching ratios and the radiative lifetime of the 4G 5/2 multiplet, were calculated. The Judd-Ofelt theory has been applied to evaluate the Ω t (t = 2, 4, 6) intensity parameters. The highest stimulated emission cross-sections for the 4G 5/2 → 6H 7/2 transition around 594 nm were calculated to be 1.67 × 10−21 cm2 for σ polarization and 1.15 × 10−21 cm2 for π polarization, with full width at half maximum (FWHM) of 7.68 nm and 7.27 nm, respectively. The fluorescence lifetime of the 4G 5/2 manifold was 1.84 ms. All the results show that Sm:LMA crystal would be a promising orange-red solid state laser material. • The most intensive absorption line of Sm3+ ion, suitable for 405 nm InGaN laser diode. • The rigidity of Sm:LMA crystal is higher than some host crystals. • The value Ω 2 of Sm:LMA crystal is comparable to Sm:LiYF 4. • The large parameter σ em τ of Sm3+ in LMA is beneficial for the solid state laser. [ABSTRACT FROM AUTHOR]