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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]

Tm3+-doped CaY 0.9 Lu 0.1 AlO 4 single crystal was successfully grown by the Czochralski method. The crystal structure, polarized absorption spectra and polarized emission spectra of Tm:CaY 0.9 Lu 0.1 AlO 4 crystals were investigated. By using the Judd–Ofelt approach, the intensity parameters Ω 2,4,6 , spontaneous transition rate, branching ratios and radiative lifetimes were calculated. Diode-end-pumped continuous-wave Tm:CaY 0.9 Lu 0.1 AlO 4 lasers have also been investigated by establishing a simple and compact plane-concave cavity with four differently coated output couplers. Four different lasing wavelengths at about 2029 nm, 2000 nm, 1966 nm and 1888 nm have been achieved with maximum output power and slope efficiency of (1.98 W, 15.1%), (5.89 W, 46.2%), (6.92 W, 54.9%) and (5.54 W, 44.7%), respectively. The results in regard to the broad emission spectra and good laser performance show that the Tm:CaY 0.9 Lu 0.1 AlO 4 mixed crystal could be very promising for broadband tunable and/or femtosecond ultrafast laser generation in the important 2-μm spectral region. • Tm:CaY 0.9 Lu 0.1 AlO 4 crystal was grown by the Czochralski method. • The crystal structure, polarized spectra were investigated. • The maximum output power of 6.92 W with slope efficiency 54.9% was achieved. [ABSTRACT FROM AUTHOR]

Ho3+-doped CaY 0.9 Gd 0.1 AlO 4 single crystal was successfully grown by the Czochralski technique for the first time. The polarized absorption spectra, polarized luminescence spectra and fluorescence decay curve of the crystal were investigated at room temperature. The spectroscopic parameters are calculated based on Judd–Ofelt theory, the values of Ω 2,4,6 were calculated to be 3.16 × 10−20 cm2, 3.93 × 10−20 cm2, 0.91 × 10−20 cm2, respectively. The Ho:CaY 0.9 Gd 0.1 AlO 4 crystal exhibits strong emission at 2013 nm for π- and 2032 nm for σ-polarizations with stimulated emission cross section of 6.64 × 10−20 cm2 and 1.90 × 10−20 cm2, respectively. The fluorescence lifetime of the 5I 7 level was measured to be 6.60 ms. The continuous-wave (CW) laser operation of Ho:CaY 0.9 Gd 0.1 AlO 4 crystal around 2 μm was demonstrated. • Ho3+-doped CaY 0.9 Gd 0.1 AlO 4 single crystal was successfully grown by the Czochralski technique for the first time. • The emission cross-section at 2013 nm and 2032 nm are 6.64 × 10−20 cm2 and 1.90 × 10−20 cm2 for π- and σ-polarizations respectively. • The continuous-wave (CW) laser operation of Ho:CaY 0.9 Gd 0.1 AlO 4 crystal around 2 μm was demonstrated. [ABSTRACT FROM AUTHOR]

High quality Pr3+ single-doped PbF 2 and Pr3+/Yb3+ co-doped PbF 2 single crystals were grown by temperature gradient technique (TGT). By co-doping Yb3+ ion as Pr3+ ions sensitizer, the visible light emission can be regulated and the largest luminescence branching ratio can be switched from red-orange to blue-green light. Besides, when Pr3+ ions doping concentration is as low as possible, the blue light self-absorption effect can be weakened, which is beneficial to high-efficiency blue laser output. Moreover, the broad band emission around 1.3 μm from 1G 4 energy level can be observed in the Pr3+/Yb3+:PbF 2 crystal with the low maximum phonon energy for the first time. Absorption, emission spectra and luminescence mechanism are well analyzed by the energy transfer process and J-O theory. The laser upper energy level lifetime of Pr3+ ions has a great increase by Yb3+ ion effect. These advantageous spectroscopic characteristics show that the Pr3+/Yb3+:PbF 2 crystal might be potential laser gain materials for blue-green and ∼1.3 μm near-IR laser operation. • By co-doping Yb3+ ion as sensitizer for Pr3+ ions, the visible light emission can be regulated and the largest luminescence component ratio can be changed from red-orange light to blue-green light. • When doping concentration of Pr3+ ion is as low as possible, the self-absorption effect of blue light can be weakened, which is beneficial to high-efficiency blue laser output. • The broad band emission around 1.3 μm from 1G 4 energy level can be observed in the Pr3+/Yb3+: PbF 2 crystal with the low maximum phonon energy for the first time. [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]

Tm3+, Pr3+ co-doped Bi 4 Ge 3 O 12 (Tm,Pr:BGO) crystals with various Pr3+ doping concentration were successfully grown using the micro-pulling-down (μ-PD) method. The use of Pr3+ co-doping for deactivating the Tm3+ ions at 1.5 μm emission was investigated in the BGO single crystal for the first time. The effect of Pr3+ concentration on the spectroscopic properties of Tm,Pr:BGO crystals were demonstrated. In addition, the fluorescence lifetime of Tm3+:3F 4 level of 0.5 at.% Pr, 2 at.% Tm:BGO crystal was quenched effectively (from 5.64 ms down to 0.36 ms) and the population inversions between Tm3+:3H 4 and 3F 4 levels are enhanced to achieve a four-level laser system at 1.5 μm. • Tm,Pr:BGO crystals with different Pr3+ concentration were grown using by the micro-pulling-down method. • The effect of Pr3+ concentration on the spectroscopic properties of Tm,Pr:BGO crystals was studied. • The use of Pr3+ co-doping for deactivating the Tm3+ ions at 1.5 μm emission was investigated in BGO crystal. [ABSTRACT FROM AUTHOR]

A Nd:BGSO crystal with the dimensions of Φ2 × 131 mm3 has been grown successfully by the micro-pulling-down method. The peak absorption cross-section at 808 nm was calculated to 0.98 × 10−20 cm2 with full-width at half-maximum of 17.4 nm. The stimulated emission cross-section was obtained to be 3.15 × 10−20 cm2 at 1063 nm. The fluorescence and radiative lifetimes of 4F 3/2 level were 248 μs and 300 μs respectively. All results indicate that the Nd: BGSO single crystal would be a promising near-IR solid-state laser material. [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]