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Yb:CaYAlO 4 (Yb:CALYO) shaped crystal fibers with different Yb3+ doping concentration were successfully grown by the micro-pulling-down (μ -PD) method. The effect of the Yb3+ concentration on the structure, absorption, emission and lifetime was systematically studied. The strongest absorption peaks of Yb:CALYO crystal fibers are located at 977 nm for σ and π polarization. The micro-photoluminescence indicate that Yb3+ ions in CALYO single crystal fiber grown by the μ -PD method distributed evenly across a cross-section. The emission cross-section of 5 at.% Yb:CALYO crystal fiber was calculated to be 0.86 × 10−20 and 1.08 × 10−20 cm2 at 983 nm for σ and π polarizations. Benefited from the disordered structrure of CaYAlO 4 crystal, the full width at half maximum (FWHM) at 978 nm was 68.9 nm and 80.9 nm, respectively. The fluorescence lifetime of 2F 5/2 energy level of Yb:CALYO crystal fibers with concentration of 0.5 at.%, 1 at.%, 2 at.% and 5 at.% was calculated to be 435 μs, 484 μs, 514 μs and 453 μs, respectively. The experimental results show that Yb:CALYO crystal fiber is a potential laser medium for ultrashort laser operation. • Yb:CaYAlO 4 shaped crystal fibers were grown by the micro-pulling down method. • The crystal structure, polarized spectra were investigated. • The effect of Yb3+ concentration on the spectroscopic properties was evaluated. [ABSTRACT FROM AUTHOR]

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]