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We report on the characterization and first laser operation of ceramic Yb:LuScO3 in a thin-disk oscillator. The optical performance achieved with a ceramic Yb:LuScO3 disk is compared to the one obtained with an existing ceramic Yb:Lu2O3 disk for reference. The characterization covers the measurement of the fluorescence spectra, the fluorescence lifetimes, and nomarsky imaging. The investigation on the laser operation covers the measurement of resonator losses, output powers, and thermal behavior during continuous-wave operation in a multimode thin-disk oscillator. An average output power of 149 W and a slope efficiency of 51.8% were achieved with the ceramic Yb:LuScO3 disk which reached a maximum surface temperature of about 150 °C. At the same temperature level, a disk made of the already established ceramic Yb:Lu2O3 delivered 957 W of output power with a slope efficiency of 75.7%. [ABSTRACT FROM AUTHOR]

A series of high quality x%Pr3+:BaF2 (x = 0.6, 1, 2); (1%Pr3+, 2%Na+):BaF2; (1%Pr3+, y%Ca2+):BaF2 (y = 3, 5) and (0.6%Pr3+, 10%R3+):BaF2 (R = Y, Lu, Gd) crystals were grown by temperature gradient technique (TGT). The Raman spectra, absorption spectra, fluorescence spectra, and fluorescence decay lifetime were measured. XRD patterns indicate that the as-synthesized samples are pure BaF2 phase. The absorption cross-section of Pr3+ ions in the BaF2 matrix can be greatly improved by co-doping R3+ ions, while improvement by Na+ and Ca2+ ions is marginal. The fluorescence characteristic of Pr3+ ions can be effectively regulated by co-doping Na+, Ca2+, R3+ (R = Y, Lu, Gd) ions of different valence states. When R3+ ions are introduced, the fluorescence spectra show the strongest orange emission and the CIE chromaticity coordinates of Pr3+ ions are also in the orange region. When single-doped Pr3+ ions and Na+ or Ca2+ ions are introduced, the fluorescence lifetime of the 3P0 level is double exponential decay, and the short lifetime is the main proportion. However, the fluorescence centers tend to homogeneous and stable by R3+ ions co-doping and the fluorescence lifetime exhibits single-exponential decay, which is fitted to 49.7 μs, 47.8 μs and 49.6 μs of (0.6%Pr3+, 10%R3+):BaF2 (R = Y, Lu, Gd), respectively. All the results show that (Pr3+, Gd3+):BaF2 and (Pr3+, Na+):BaF2 are excellent laser gain media for high-efficiency orange and red laser operation. [ABSTRACT FROM AUTHOR]

The absorption spectrum, fluorescence spectrum and fluorescence time of a mixed sesquioxide Nd:LuYO 3 ceramic were measured at room temperature. Judd-Ofelt theory was applied to calculate the spectral parameters of Nd:LuYO 3. The absorption cross section at 812 nm was calculated to be 0.99 × 10−20 cm2 with full width at half maximum (FWHM) of 47.69 nm. The emission cross-section at 1077 nm was calculated to be 5.24 × 10−20 cm2 with FWHM of 11.62 nm. The fluorescence lifetime and quantum efficiency of the 4F 3/2 multiplet were determined to be 228.4 μs and 85.2%, respectively. Continuous-wave (CW) laser operation of Nd:LuYO 3 ceramic was demonstrated. Simultaneous laser operation at 1075.24 and 1080.03 nm was achieved with maximum output power of 490 mW and slope efficiency of 6.36%. • Nd:LuYO3 ceramic was fabricated by solid-state reaction. • Judd-Ofelt theory was used to analyze the spectroscopic properties of Nd:LuYO 3 ceramic. • CW laser operation was performed and output power of 490 mW at the absorbed power of 9.1 W is obtained. [ABSTRACT FROM AUTHOR]

YScO 3 single crystal co-doped with Ho3+ and Pr3+ ions has been successfully grown by the Czochralaki method. The absorption spectrum, fluorescence spectrum and fluorescence decay curve were measured at room temperature. The absorption cross section of Ho,Pr:YScO 3 at 649 nm and 1130 nm was calculated to be 0.93 × 10−20 cm2 and 0.32 × 10−20 cm2, respectively. Judd-Ofelt (J-O) theory was performed to evaluate the spontaneous emission probabilities and the radiative lifetimes. Ho,Pr:YScO 3 exhibited strong emission at 2040 nm and 2890 nm with a emission cross section of 0.80 × 10−21 cm2 and 1.22 × 10−20 cm2, respectively. The fluorescence lifetime of the Ho3+:5I 6 and 5I 7 levels were calculated to be 0.31 ms and 5.89 ms, respectively. All the results indicate that the Ho,Pr:YScO 3 crystal could be a potential laser material for 2.9 μm laser operation. • Ho3+,Pr3+ co-doped YScO 3 was grown by the Czochralski method. • The crystal structure, absorption and emission spectra were investigated. • The effect of Pr3+ on the spectroscopic properties of Ho3+ was evaluated. [ABSTRACT FROM AUTHOR]

Sm:YAlO 3 (Sm:YAP) crystal with size of Φ28 × 80 mm3 was grown by Czochralski (Cz) method. Polarized absorption spectra and fluorescence spectra of Sm:YAP crystal were discussed for the first time. The peak emission cross-sections were calculated to be 0.80 × 10−21 cm2 (604 nm for a-polarization), 1.82 × 10−21 cm2 (604 nm for b-polarization) and 1.63 × 10−21 cm2 (610 nm for c-polarization), respectively. The Judd-Ofelt (JO) intensity parameters were calculated to be Ω 2 = 2.59 × 10−20 cm2, Ω 4 = 1.78 × 10−20 cm2 and Ω 6 = 2.98 × 10−20 cm2, respectively. The decay lifetime of 4G 5/2 energy level was measured to be 2.51 ms. All above results indicate the Sm:YAP crystal may be a potential candidate of reddish-orange laser pumped directly by the GaN/InGaN laser diode. • Sm:YAlO 3 crystal was grown by Cz method. • Polarized optical spectra of Sm:YAlO 3 crystal were investigated. • The transitions of 4G 5/2 → 6H 7/2 have the highest branching ratio value, which is suitable for reddish-orange laser. [ABSTRACT FROM AUTHOR]

Tm3+-doped calcium niobium gallium garnet (Tm:CNGG) single crystals have been successfully grown by the micro-pulling-down (μ-PD) method. The crystal structure, absorption spectra, fluorescence spectra and lifetimes of Tm:CNGG crystals were investigated. The absorption and emission bandwidths of Tm:CNGG crystals are larger than those of other Tm3+ doped garnet crystals, which will be beneficial for laser diode (LD) pumping and ultrashort pulse generation. Additionally, continuous wave (CW) laser operation around 2 μm was achieved in the 2.0 at.% Tm:CNGG crystal by LD pumping. [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]

Tm3+-doped CaYAlO 4 (Tm:CALYO) shaped crystals fibers with various doping concentration of 2 at.%, 3 at.%, 5 at.% and 7 at.% have been successfully grown by the micro-pulling-down (μ -PD) method. The polarized absorption spectra, polarized fluorescence spectra and fluorescence decay curves were analyzed at room temperature. The absorption bands of 3H 6 →3H 4 transition centered at around 800 nm match well with commercial AlGaAs laser diode pumping sources. For 7 at.% Tm:CALYO crystal fiber, the full width at half maximum (FWHM) of the emission band for π polarization at 1806 nm was 225.4 nm. The fluorescence of 3F 4 level decreased strongly as the thulium concentration increased. All the results indicate that Tm:CALYO crystal fibers are promising for ultrashort and tunable laser operation. • Tm:CALYO shaped crystal fibers were grown by the micro-pulling-down technique for the first time. • The full width at half maximum (FWHM) of the emission band for π polarization at 1806 nm was calculated to be 225.4 nm. • The fluorescence lifetime was calculated to be 4.11, 3.74, 3.55 and 2.90 ms for doping concentration of 2, 3, 5 and 7 at.%, respectively. [ABSTRACT FROM AUTHOR]

A series of 0.5 at.% Tm:Ca 1-x Y x F 2+x (x = 0, 0.01, 0.04, 0.06, 0.08, 0.12) crystals have been successfully grown by the temperature gradient technique (TGT) method. The absorption spectra, fluorescence spectra, and fluorescence decay curves were measured and analyzed at room temperature. By comparison, it is found that when the concentration of Y3+ ions reaches 8 at.%, the absorption cross section corresponding to the 3H 6 →3H 4 energy level is 2.56 × 10−21 cm2 at 793 nm, which is suitable for GaAlAs LD pumping. The J-O strength parameters Ω 2 , Ω 4 , and Ω 6 were obtained. With the incorporation of Y3+ ions, the value of Ω 4 /Ω 6 gradually increases. When the concentration of Y3+ ions reaches 8 at.%, the emission cross sections are 3.05 × 10−21 cm2 at 1476 nm, 2.56 × 10−21 cm2 at 2378 nm, and the full widths at half maximum (FWHM) are 76 nm and 195 nm, respectively. The fluorescence lifetime of 3H 4 level, the upper level of 1.5 μm and 2.3 μm, is 1.05 ms, which is very beneficial for 1.5 μm and 2.3 μm laser. • With the incorporation of Y3+ ions, the value of Ω 4 /Ω 6 gradually increases. • When the concentration of Y3+ ions reaches 8 at.%, the emission cross section is 3.05 × 10−21 cm2 at 1476 nm, 2.56 × 10−21 cm2 at 2378 nm, respectively. • The fluorescence lifetime of 3H 4 level, the upper level of 1.5 μm and 2.3 μm, is 1.05 ms, which is very beneficial for 1.5 μm and 2.3 μm laser. [ABSTRACT FROM AUTHOR]

Yb,Tb:YAG crystals with various Yb3+ and Tb3+ concentration were grown by the micro-pulling-down method (μ -PD). The absorption spectra, fluorescence spectra and fluorescence decay curves of Yb,Tb:YAG crystals were measured at room temperature. Under 980 nm excitation, Yb,Tb:YAG crystals exhibited intense visible up-conversion luminescence due to the cooperative energy transfer from two Yb3+ ions to one Tb3+ ion. Under 485 nm excitation, Yb,Tb:YAG crystals yielded near-infrared down-conversion emission, ascribing to the cooperative absorption of pumping photons and cooperative energy transfer from one Tb3+ ion to two Yb3+ ions. The energy transfer processes from Yb3+ ions to Tb3+ ions were discussed, and the energy transfer efficiency was calculated. Based on studies of the obtained results, Yb3+/Tb3+ co-doped YAG crystal shows promising potential for sensing, volumetric displays, optical data storage, light emitting diodes. • Yb,Tb:YAG single crystals grown by the micro-pulling-down technique. • The cooperative energy transfer process was analyzed. • The effect of doped concentration on energy transfer efficiency was discussed. [ABSTRACT FROM AUTHOR]

• After co-doping Tb3+ ions, the Ω4/Ω6 increased 1.57 from to 1.66. • The branching ratios of the 3H 4 →3F 4 transition also strengthened. • The decay curve of 3F 4 level doped with different Tb3+ ions concentration decreased. • Tb3+ ion is a productive deactivator that could reduce the filling of 3F 4 mainfold and enhance the emission of 3H 4 →3F 4 transition. Tm3+ and Tb3+ co-doped Y 3 Al 5 O 12 (YAG) ceramics were fabricated by high temperature solid state reaction under oxygen sintering. The absorption spectra, fluorescence spectra and fluorescence decay curves of Tm,Tb:YAG ceramics were measured. The spectral parameters of Tm,Tb:YAG ceramic were calculated. The lifetimes of Tm3+:3F 4 level of Tm,Tb:YAG ceramics were calculated to be 11.28, 2.12, 1.24, 0.63 and 0.49 ms for the Tb3+ doping concentration of 0, 0.1, 0.2, 0.35 at 0.5 at%, respectively. The co-doping Tb3+ ion is a productive deactivator that could reduce the filling of 3F 4 mainfold and enhance the emission of 3H 4 →3F 4 transition. These results indicate that the addition of Tb3+ ions in Tm,Tb:YAG ceramic could be a promising technique for laser operation around 1.5 µm. [ABSTRACT FROM AUTHOR]

• A series of 0.6 at% Pr:CaF 2 -RF 3 (R= Y3+, Gd3+, Lu3+) crystals were successfully grown by the temperature gradient technique(TGT) method. • By co-doping R3+ ion (R=Y3+, Gd3+, Lu3+), the spectral performance of the crystals could be significantly improved and the function effect is also different. • The spectral performance and spectral quality factor of the crystals were systematically described and compared for the first time. • The spectral modulation effect caused by Y3+, Gd3+ and Lu3+ co-doping ion was discussed. A series of 0.6 at% Pr:CaF 2 -RF 3 (R = Y3+, Gd3+, Lu3+) crystals have been successfully grown by the temperature gradient technique(TGT). The absorption spectra, fluorescence spectra, and fluorescence decay curves were measured and analyzed at room temperature. When the R3+ concentration is higher than a certain value, the diffraction peaks of Pr:CaF 2 -RF 3 crystals were well indexed to the (Ca,Y)F 2 phase. By co-doping R3+ ion (R=Y3+, Gd3+, Lu3+), the spectral performance of the crystals could be significantly improved and the function effect is also different. For 0.6 at% Pr, 28.5 at% Y:CaF 2 crystal, the fluorescence lifetime of 3P 0 energy level was fitted to be 45.46 µs, and the emission cross sections of 3P 0 →3H 6 (605 nm), and 3P 0 →3F 2 (641 nm) were calculated to be 1.78 × 10−20 cm2, and 4.61 × 10−20 cm2 with the full width at half (FWHM) of 20.1 nm and 6.8 nm, respectively. The 0.6 at% Pr, 28.5 at% Y:CaF 2 crystal could be favorble laser medium for ultra-fast laser opreration at 605 nm and 641 nm. For 0.6 at% Pr, 18 at% Gd:CaF 2 and 0.6 at% Pr, 10 at% Lu:CaF 2 crystals, the spectral quality factors σ em• τ f of 3P 0 →3F 2 transition (642 nm) were calculated to be 614.18 × 10−20 cm2•µs and 506.36 × 10−20 cm2•µs with the FWHM of 3.7 nm and 5.3 nm. All the results show that 0.6 at% Pr, 18 at% Gd:CaF 2 and 0.6 at% Pr, 10 at% Lu:CaF 2 crystals are promising gain media for high-efficiency visible laser output at 642 nm, which would compete with commercial Pr: YLF crystal in the future. [ABSTRACT FROM AUTHOR]

Abstract: Nd,Co:LaMgAl11O19 (abbreviated as Co,Nd:LMA) was grown using the Czochralski method. The structure, polarized absorption spectrum, fluorescence spectrum, and fluorescence decay time were analyzed. The as-grown crystal had very wide absorption bands at 794nm, which can be pumped by GaAs laser diode without temperature stabilization. Two strong emission bands were present at 1056nm and 1082nm with full-width at half-maximum (FWHM) of 6 and 8nm, respectively. The large FWHM is due to the inhomogeneity of the Nd ion sites. The lifetimes of the 4F3/2 manifold of Co,Nd:LMA at room temperature monitored at 905nm, 1056nm, and 1344nm were 292, 288, and 350μs, respectively, which was caused by the different contribution of the three different sites with D3h and C2v symmetry. The absorption band of Co is from 1.3μm to 1.6μm, and Co,Nd:LMA still has a strong emission around the 1.38μm, indicating that the Co,Nd:LMA can be applied as a potential self-Q-switched material operating at 1.3μm. [Copyright &y& Elsevier]

Tm3+-doped bismuth germanate crystals (Tm:BGO) with various doping concentrations of 0.5, 0.75, 1.0, 1.5, and 2.0 at.% were grown by the micro-pulling-down method (μ-PD). The effect of thulium concentration on the growth, structure, absorption spectra, emission spectra and fluorescence lifetime of 3H 4 and 3F 4 state was studied. Under excitation of 792 nm, Tm:BGO crystals exhibit two fluorescence bands corresponding to the 3H 4 → 3F 4 and the 3F 4 → 3H 6 transitions. The fluorescence lifetime of 3H 4 state decreased strongly as the thulium concentration increased, while the lifetime of 3F 4 state was relatively constant for all thulium concentrations. • Tm:BGO crystals with different Tm3+ concentration were grown by the micro-pulling-down method. • The effect of Tm3+ concentration on the growth, structure and spectroscopic properties of Tm:BGO crystals was studied. • Tm:BGO crystals exhibit two fluorescence bands corresponding to the 3H 4 → 3F 4 and the 3F 4 → 3H 6 transitions. [ABSTRACT FROM AUTHOR]

Tm3+ doped and Tm3+, Pr3+ co-doped Lu 3 Al 5 O 12 (LuAG) garnet single crystals have been successfully grown by the micro-pulling-down (μ-PD) method. The absorption spectra, fluorescence spectra and lifetimes were investigated at room temperature. In the absorption spectra, the transition centered at 782 nm matches well with the GaAlAs LDs laser pumping. The incorporation of Pr3+ into Tm3+-doped LuAG crystals enhanced the intensity of 1.5 μm emission and decreased the fluorescence lifetime of the lower energy level for 1.5 μm emission from 10.427 ms to 2.603 ms. The results indicate that Tm,Pr:LuAG crystal can be promising candidate for near infrared 1.5 μm laser materials. • Tm:LuAG and Tm,Pr:LuAG crystals have been successfully grown by the micro-pulling-down (μ-PD) method. • Spectral parameters of Tm:LuAG and Tm,Pr:LuAG crystals were obtained and compared. • The fluorescence mechanism of Tm,Pr:LuAG crystal has been studied for the first time. [ABSTRACT FROM AUTHOR]

Nd:SrAl 11 O 19 (Nd:SRA) crystal has been grown by the Czochralski method. Polarized absorption spectra, polarized fluorescence spectra and fluorescence lifetime were investigated. For σ-polarization, the peak absorption cross section at 798 nm is 2.08 × 10−20 cm2 with full width at half maximum (FWHM) of 10.2 nm and the peak emission cross section is 3.36 × 10−20 cm2 at 1048.5 nm with FWHM of 4.80 nm. The Judd-Ofelt parameters Ω 2,4,6 were obtained to be 0.51 × 10−20 cm2, 2.08 × 10−20 cm2, and 2.12 × 10−20 cm2, respectively. Continuous-wave laser operation of the a-cut and c-cut Nd:SRA sample has been demonstrated. The maximum output power of 8.33 W was achieved from c-cut sample at an absorbed power of 27.73 W, corresponding to a slope efficiency of 31.3%. • Nd:SrAl 12 O 19 crystal has been gown by the Czochralski method. • Spectral parameters of Nd:SrAl 12 O 19 crystal were obtained. • Continuous-wave laser was demonstrated from Nd:SrAl 12 O 19 crystal. [ABSTRACT FROM AUTHOR]

Yb,Pr:CaF 2 crystals have been grown successfully by the temperature gradient technique(TGT). The absorption spectra, fluorescence spectra, fluorescence decay lifetime of Pr3+ ions in CaF 2 crystal sensitized by different Yb3+ ions concentration have been measured. The effective J-O intensity parameters were fitted to be Ω 2 =0.36 × 10−20cm2, Ω 4 =2.89 × 10−20cm2, Ω 6 =6.69 × 10−20cm2 for 0.3 at.%Pr,1.5 at.%Yb:CaF 2. And the emission cross sections of 3P 1 →3H 5 (535 nm), and 3P 0 →3F 4 (750 nm) are calculated to be 2.02 × 10−20cm2, and 2.50 × 10−20cm2 with the FWHM of 17.2 nm, and 10.5 nm, respectively. The fluorescence lifetime of 3P 0 has achieved great increasing by sensitizing of Yb3+ ion. Not only the up-conversion luminescence can be achieved, but also the broad band emission from 1D 2 energy level can be observed. The results show that Yb,Pr:CaF 2 could be a potential laser gain medium for visible and near-IR laser operation. • Not only the up-conversion luminescence can be achieved, but also the broad band emission from 1D 2 energy level can be observed by Yb3+ ion sensitizing. • Spectral properties and Judd-Ofelt parameters of Yb,Pr:CaF 2 crystal were investigated and analysed. [ABSTRACT FROM AUTHOR]

GdScO 3 single crystal codoped with Tm3+ and Tb3+ ions was successfully grown by the Edge-defined Film-fed Growth Method (EFG) for the first time. Absorption, fluorescence spectrum and fluorescence lifetimes of the grown crystal at room temperature were measured. The absorption cross-section at 789 nm was calculated to be 8.20 × 10−21 cm2. The emission cross-section was 1.35 × 10−21 cm2 at 1504 nm with the FWHM of 95.3 nm. The fluorescence lifetimes of the 3H 4 state and the 3F 4 state were fitted to be 253 μs and 1460 μs, respectively. Compared with Tm3+ single doped GdScO 3 crystal, the codoping of Tb3+ successfully depopulated the 3F 4 energy level and enhanced the emission at 1.5 μm region. It indicated that Tm,Tb:GdScO 3 could be favorable laser medium for 1.5 μm-laser operation. • Tm3+ and Tb3+ co-doped GdScO 3 crystal was successfully grown by the edge-defined film-fed method (EFG) for the first time. • Spectral parameters and Judd-Ofelt parameters of Tm,Tb:GdScO3 crystal were obtained and compared. • The fluorescence mechanism of Tm3+ and Tb3+ co-doped GdScO 3 crystal has been studied. [ABSTRACT FROM AUTHOR]

Yb,Ho:Y 2 O 3 ceramics have been fabricated by Spark Plasma Sintering method (SPS). The microstructure and transmittance of the ceramics sintered from 1623 K to 1673 K were analyzed. The highest in-line transmittance of Yb,Ho:Y 2 O 3 ceramic sintered at 1673 K reached almost 83% at 750 nm with the thickness of 1 mm. The absorption spectra, fluorescence spectra and fluorescence decay curve were recorded at room temperature. The Judd-Ofelt parameters Ω 2 , Ω 4 and Ω 6 were calculated to be 8.33 × 10−20 cm2, 1.81 × 10−20 cm2, and 0.82 × 10−20 cm2, respectively. The intense emission cross section of Yb,Ho:Y 2 O 3 ceramic was 3.43 × 10−20 cm2 at 2057 nm with full width at half maximum (FWHM) of 208 nm. The results indicate that Yb,Ho:Y 2 O 3 transparent ceramic can be a promising laser gain medium for laser operation around 2 μm. Image 1 • The highest in-line transmittance of Yb,Ho:Y 2 O 3 ceramic sintered at 1673 K reached almost 83% at 750 nm with the thickness of 1 mm. • The spectral characteristics were intensively investigated through Judd-Ofelt theory. [ABSTRACT FROM AUTHOR]

Photograph of Yb,Ho:YAG crystals grown by the μ-PD method. (a) Yb = 0.05, (b) 0.1, (c) 0.15. • Y 3 Al 5 O 12 (YAG) single crystals doped with a fixed Ho3+ content of 0.5 at.% and various Yb3+ contents (Yb = 5, 10 and 15 at.%) have been successfully grown by the micro-pulling-down (μ-PD) method. Y 3 Al 5 O 12 (YAG) single crystals doped with a fixed Ho3+ content of 0.5 at.% and various Yb3+ contents (Yb = 5, 10 and 15 at.%) have been successfully grown by the micro-pulling-down (μ-PD) method. The absorption spectra, fluorescence spectra and fluorescence decay curves were recorded at room temperature. The intense emission of Yb,Ho:YAG crystal centered at 2 μm corresponds to the 5I 7 → 5I 8 transition. Three intense emissions centered at 524–569 nm, 623–691 nm and 744–746 nm, correspond to the 5F 4 + 5S 2 → 5I 8 , 5F 5 → 5I 8 and 5F 4 + 5S 2 → 5I 7 transitions, respectively. The possible energy transfer mechanisms were discussed intensively. [ABSTRACT FROM AUTHOR]

High quality 7 at%Er:Y 2 O 3 crystal was successfully grown by Fz method. Judd-Ofelt theory was applied to analyze spectroscopic properties at 2.7 μm. The larger value of Ω 2 shows low local environment symmetry exists in Er:Y 2 O 3 crystal, and the large Ω 4 /Ω 6 indicates better spectral quality. The larger absorption cross-section and FWHM are beneficial to efficient absorption of pump source. The fluorescence spectra and lifetimes of Er:Y 2 O 3 crystal were measured and studied at 2.7 μm. The emission cross-sections at 2723 nm was calculated to be 1.41 × 10−20cm2. Compared with other Er3+ doped crystals, the large spectral quality factors Q and low fluorescence lifetime ratio illustrate that Er:Y 2 O 3 crystal has excellent laser properties at 2.7 μm. In addition, the low inversion ratio also indicates great potential of Er:Y 2 O 3 crystal for laser generation at 2.7 μm. • A high quality 7%Er:Y 2 O 3 laser crystal was successfully grown by Fz method. • Judd-ofelt (J-O) parameterization scheme was applied to analyze the spectroscopic properties of 7%Er:Y 2 O 3 laser crystal at 2.7 μm. • The large spectral quality factors Q with low fluorescence lifetime ratio illustrates that Er:Y 2 O 3 crystal has excellent laser properties at 2.7 µm. • The low inversion ratio indicates great potential of Er:Y 2 O 3 crystal for laser generation at 2.7 μm. [ABSTRACT FROM AUTHOR]

Dy3+-doped Y 3 Al 5 O 12 (YAG) and Y 3 ScAl 4 O 12 (YSAG) single crystals have been successfully grown by the micro-pulling-down (μ-PD) technique for the first time. The room temperature absorption spectra, fluorescence spectra and fluorescence decay curves were measured. Dy:YAG and Dy:Y 3 ScAl 4 O 12 crystals exhibit strongest emission centered at 583 nm, corresponding to the 4F 9/2 → 6H 13/2 transition. The decay lifetime of the 4F 9/2 level was measured to be 634 μs and 667 μs, respectively. All these results indicate that the Dy:YAG and Dy:Y 3 ScAl 4 O 12 crystals are promising candidates for yellow laser operation. • Dy:YAG and Dy:YSAG crystals were grown by the micro-pulling-down method. • Dy:YAG and Dy:YSAG crystals exhibit strong emission centered at 583 nm. • Dy:YSAG crystal has a wide emission bandwidth due to the disordered crystalline structure. [ABSTRACT FROM AUTHOR]