Growth and spectral properties of Gd2SiO5 crystal codoped with Er and Yb

Gd2SiO5 (GSO) single crystal codoped with Yb3+ and Er3+ (Abbr. as Er:Yb:GSO) was successfully grown by the Czochralski (CZ) method for the first time and the spectral characteristics were investigated. The absorption and fluorescence spectra were measured. The emission lifetime of the I-4(13/2)-Er-level was measured to be 5.84ms and the emission cross-section at 1529nm was calculated to be 1.03 x 10(-20) cm(2). The results indicate that Er:Yb:GSO is a potential laser material at similar to 1. 55 mu m wavelength region. (c) 2006 Elsevier B.V. All rights reserved.

Gain and noise figure of a double-pass waveguide amplifier based on Er/Yb-doped phosphate glass

A waveguide amplifier is fabricated by Ag+-Na+ two-step ion exchange on Er/Yb-doped phosphate glass. The spectroscopic performance of glass and the properties of channel waveguide are characterized. A double-pass configuration is adopted to measure the gain and noise figure (NF) of the waveguide amplifier, and the comparison of gain and NF for the single and double-pass configuration of the waveguide amplifier is presented. The results show that the double-pass configuration can make the gain increase from 8.8dB (net gain 2.2dB/cm) of the single-pass one to 14.6 dB (net gain 3.65 dB/cm) for small input power at 1534 nm, and the NF are all lower than 5.5dB for both the configurations.

Growth and spectroscopic characteristics of Yb : GSO single crystal

For the first time, a high optical quality 10 at.% Yb3+-doped gadolinium oxyorthosilicate laser crystal Gd2SiO5 (GSO) was grown by the Czochralski (Cz) method. The segregation coefficient of Yb3+ was studied by the inductively coupled plasma atomic emission spectrometer (ICP-AES) method. The crystal structure has monoclinic symmetry with space group P2(1)/c; this was determined by means of an x-ray diffraction analysis. The absorption spectra, fluorescence spectra and fluorescence decay curves of Yb3+ ions in a GSO crystal at room temperature were also studied. Then, the spectroscopic parameters of Yb:GSO were calculated. The advantages of the Yb:GSO crystal include high crystal quality, quasi-four-level laser operating scheme, high absorption cross-sections and particularly broad emission bandwidth (similar to 72 nm). The results indicated that the Yb:GSO crystal seemed to be a very promising laser gain medium in diode-pumped femtosecond laser and tunable solid state laser applications when LD pumped at 940 and 980 nm.

LD抽运Yb:GSO实现1090nm低阈值激光运转

We report what we believe to be the first demonstration of laser operation with a novel laser material of Yb3(+) -doped Gd-2 SiO2 (Yb: GSO) pumped by a laser diode at 940 nm. We obtained a low lasing threshold of 1.27 kW/cm(2) with the center wavelength of 1090 nm, which is lower than the value of 1.53 kW/cm(2) predicted for Yb: YAG. The maximal output power of 360 mW was obtained with a 2% output, which corresponds to a slope efficiency up to 19%.

Characterization of diode-pumped laser operation of a novel Yb : GSO crystal

We report what is believed to be the first demonstration of the laser action of Yb3+ -doped Gd2SiO5 (Yb:GSO) crystal pumped by a 940-nm laser diode at room temperature. The threshold of laser generation is only 0.85 kW/cm(2), which is smaller than the theoretic threshold of Yb:YAG (1.54 kW/cm(2)). The laser wavelength is 1090 mn. With a 2.5% output coupler, the maximum output power is 415 mW under a pump power of 5 W. By using the SESAM, the Q-switched mode locking and CW mode-locked operations are demonstrated.

激光二极管抽运的高效率低阈值Yb：GSO激光器

近年来，掺Yb离子的晶体备受关注：掺Yb离子晶体能级结构简单，可以避免激发态再吸收、频率上转换、弛豫振荡和浓度猝灭等效应。此外，掺Yb离子晶体的吸收光谱位于900～1000nm，无需严格的温度控制即可与InGaAs激光二极管有效耦合，并且具有很宽范围的荧光发射谱，因此这种晶体很有潜力成为1gm波段的宽调谐及超快激光光源。

激光二极管抽运的Yb：GSO连续锁模激光

作为发射在1μm波段的二极管抽运全固态激光器的增益介质，掺Yb离子的晶体备受关注。掺Yb晶体具有能级结构简单，量子缺陷低（〈0．1），量子效率高等优点。目前成功使用掺Yb的晶体作为增益介质的飞秒激光振荡器已有很多报道，如Yb：BOYSE，Yb：KYW，Yb：SYSE等。

激光二极管抽运的Yb：GSO飞秒激光器

作为1μm附近由激光二极管直接抽运的高效、紧凑固体激光器的增益介质，掺Yb^3＋离子的激光材料越来越受到人们的关注。掺Yb的晶体具有能级结构简单，荧光寿命长，量子缺陷低等优点。掺Yb离子的激光晶体作为增益介质的飞秒激光振荡器国际上已有报道，实现全固态飞秒激光器件的实用化是国内外科学家追求的目标。

激光二极管抽运新型Yb：GSO晶体实现激光运转

作为发射波段在1μm的激光二极管(LD)抽运全固态激光器的增益介质，掺Yb晶体非常大的具有吸引力。Yb离子具有简单的电子结构，预防了激发态重复吸收、上转换以及浓度淬灭带来的激光损耗。而且，掺Yb介质的量子缺陷比较低可以产生相对大的斜效率和低热负载。近年来，掺Yb介质一些有效的激光运转已经得到证明，如Yb：YAG，Yb：YAB以及Yb：BOYS等。迄今为止，人们仍在进行各种尝试以得到发射荧光谱宽，低阈值运转的激光晶体。

Diode-pumped Yb : GSO femtosecond laser

Compact femtosecond laser operation of Yb:Gd2SiO5 (Yb:GSO) crystal was demonstrated under high-brightness diode-end-pumping. A semiconductor saturable absorption mirror was used to start passive mode-locking. Stable mode-locking could be realized near the emission bands around 1031, 1048, and 1088 nm, respectively. The mode-locked Yb: GSO laser could be tuned from one stable mode-locking band to another with adjustable pulse durations in the range 1 similar to 100 ps by slightly aligning laser cavity to allow laser oscillations at different central wavelengths. A pair of SF10 prisms was inserted into the laser cavity to compensate for the group velocity dispersion. The mode-locked pulses centered at 1031 nm were compressed to 343 fs under a typical operation situation with a maximum output power of 396 mW. (c) 2007 Optical Society of America.

H[DEHP]从不同介质中萃取稀土（III）(Sc、Y、Ho、Er、Yb、Lu)及Fe(III)、Zn(II)的机理

本文分另研究了H[DEHP]从不同酸性介质中萃取稀土（III）(Sc、Y、Ho、Er、yb、Lu)及Fe(III)、Zn(II)的机理及性能。一、H[DEHP]从 H_2SO_4介质中萃取Sc(III)的机理 1. H[DEHP]萃取H_2SO_4及其机理 2. H[DEHP]萃取Sc(III)的机理，用斜率法和饱和法确定了H[DEHP]的正庚烷溶液从H_2SO_4溶液中萃取Sc_2(SO_4)_3的机理及萃合物组成。研究表明，H[DEHP]萃取Sc(III)在高、低两种酸度范围内存在着两种不同的萃取机理。二、H[DEHP]从HCl介质中萃取Ln(III)和Fe(III)的性能及H[DEHP]萃取Ln(III)的机理研究了H[DEHP]的正庚烷溶液从HCl介质中萃取稀土（III）(Sc、Y、Ho、Er、Yb、Lu)和Fe(III)的性能，得出H[DEHP]在相同条件下萃取以上各金属离子的顺序是：Sc(III)>Fe(III)>Lu(III)>Yb(III)>Er(III)>Y(III)>Ho(III), 并计算了各金属离子之间的分离因素（β）。文中还讨论了Sc(III)、Fe(III)、Lu(III)之间的分离以及重稀土离子间的萃取分离，同时与相同实验条件下HEH[EHP]的萃取性能进行了比较，为新的萃取体系提供了一些参数。三、H[DEHP]从不同介质中萃取Fe(III)的机理，研究了H[DEHP]的正率烷溶液从Hcl介质中和H[DEHP]的正庚烷溶液从H_2SO_4介质中萃取Fe(III)的平衡规律；用斜率法、饱和法以及IR和NMR谱等讨论了低酸度下的萃取机理。四、H[DEHP]萃取Zn(II)的机理，研究了H[DEHP]的正率烷溶液从Hcl介中萃取Zn(II)的平衡，利用斜率法、饱和法及SR、NMR谱等讨论了低Hcl浓度下的萃取机理。

Syntheses and crystal structures of bis(tetrahydrofurfurylindenyl) lanthanocene chlorides (C4H7OCH2C9H6)(2)LnCl (Ln = Nd, Sm, Dy, Ho, Er, Yb)

Reaction of anhydrous lanthanide trichlorides with tetrahydrofurfuryl indenyl lithium in THF afforded bis(tetrahydrofurfurylindenyl) lanthanocene chlorides complexes (C4H7OCH2C9H6)(2) LnCl, Ln = Nd (1), Sm (2), Dy (3), Ho (4), Er (5), Yb (6). The X-ray crystallographic structures of all the six complexes were determined and these indicate that they are unsolvated nine-coordinate monomeric complexes with a trans arrangement of both the sidearm and indenyl rings in the solid state. They belong to the same crystal system (orthorhombic) and space group (P2(1)2(1)2(1)) with the same structure. Especially, they are more stable to air and moisture than the corresponding unsubstituted indenyl lanthanide complexes.

Novel Near-Infrared Luminescent Hybrid Materials Covalently Linking with Lanthanide [Nd(III), Er(III), Yb(III), and Sm(III)] Complexes via a Primary beta-Diketone Ligand: Synthesis and Photophysical Studies

A series of novel, colorless, and transparent sot-gel derived hybrid materials Ln-DBM-Si covalently grafted with Ln(DBM-OH)(3)center dot 2H(2)O (where DBM-OH = o-hydroxydibenzoylmethane, Ln = Nd, Er, Yb, and Sin) were prepared through the primary beta-diketone ligand DBM-OH. The structures and optical properties of Ln-DBM-Si were studied in detail. The investigation results revealed that the lanthanide complexes were successfully in situ grafted into the corresponding hybrids Ln-DBM-Si. Upon excitation at the maximum absorption of ligands, the resultant materials displayed excellent near-infrared luminescence.

Near-infrared luminescent mesoporous materials covalently bonded with ternary lanthanide [Er(III), Nd(III), Yb(III), Sm(III), Pr(III)] complexes

New near-infrared-luminescent mesoporous materials were prepared by linking ternary lanthanide (Er3+, Nd3+, Yb3+, Sm3+, Pr3+) complexes to the ordered mesoporous MCM-41 through a functionalized 1,10-phenanthroline (phen) group 5-(N,N-bis-3-(triethoxysilyl)propyl)ureyl-1,10-phenanthroline. The resulting materials (denoted as Ln(hfth)(3)phen-M41 and Pr(tfnb)(3)phen-M41; Ln=Er, Yb, Nd, Sm; hfth = 4,4,5,5,6,6,6-heptafluoro-1-(2-thienyl)hexane-1,3-dionate; tfnb = 4,4,4-trifluoro-1-(2-naphthyl)- 1, 3-butanedionate) were characterized by powder X-ray diffraction, N-2 adsorption/desorption, and elemental analysis. Luminescence spectra of these lanthanide-complex functionalized materials were recorded, and the luminescence decay times were measured. Upon excitation at the absorption of the organic ligands, all these materials show the characteristic NIR luminescence of the corresponding lanthanide (Er3+, Nd3+, Yb3+, Sm3+, Pr3+) ions by sensitization from the organic ligands moiety. The good luminescent performances enable these NIR-luminescent mesoporous materials to have possible applications in optical amplification (operating at 1300 or 1500 nm), laser systems, or medical diagnostics.