首页 | 本学科首页   官方微博 | 高级检索  
相似文献
 共查询到20条相似文献,搜索用时 31 毫秒
1.
Cu:LiNbO3 crystal and Fe:Cu:LiNbO3 crystals were grown by the Czochralski method from congruent melt. The OH absorption spectrum of doped lithium niobate crystals was measured. The photorefractive properties of doped crystals were studied by the two‐wave coupling method. The results of the two‐wave coupling experiments showed that as the concentration of doping ions increased, the diffraction efficiency and the dynamic range enhanced, the holographic response time shortened. The recording time of Fe(0.10wt%): Cu(0.10wt%): LiNbO3 crystal is only a tenth of that of Cu(0.05wt%): LiNbO3 crystal. Among all samples, the dynamic range of the Fe(0.10wt%): Cu(0.10wt%): LiNbO3 crystal was the most largest (up to 40.78). (© 2007 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)  相似文献   

2.
Mg:Ru:Fe:LiNbO3 crystals with various doping concentration of MgO have been grown by Czochralski method. The type of charge carriers and photorefractive properties in Mg:Ru:Fe:LiNbO3 crystals were measured by two‐wave coupling method using Kr+ laser (476 nm) and He‐Ne laser (633 nm) as light sources. We found that holes were the dominant charge carriers under blue light irradiation while electrons were the dominant charge carriers under red light irradiation. Mg2+ ions behaved no longer as damage resistant, but promoter to the photorefractive properties at 476 nm wavelength. The photorefractive properties under blue light improved with the increase concentration of Mg2+ ions. The enhancement mechanisms of the blue photorefractive were suggested. Experimental results definitely showed that Mg‐doped two‐centre Ru:Fe:LiNbO3 was a promising blue photorefraction material for holographic volume storage.  相似文献   

3.
In this paper, photorefractive properties of Mg:Ce:Cu:LiNbO3 crystals were studied. The crystals doped with different concentration of Mg ions have been grown by the Czochralski method. Mg concentrations in grown crystals were analyzed by an inductively coupled plasma optical emission spectrometry (ICP‐OE/MS). The crystal structures were analyzed by the X‐ray powder diffraction (XRD), ultraviolet‐visible (UV‐Vis) absorption spectra and infrared (IR) transmitatance spectra. The photorefractive properties of crystals were experimentally studied by using two‐beam coupling. In this experiment we determined the writing time, maximum diffraction efficiency and the erasure time of crystals samples with He‐Ne laser. The results showed that the dynamic range (M/#), sensitivity (S) and diffraction efficiency (η) were dependent on the Mg doping concentration, and the Mg(4.58mol%):Ce:Cu:LiNbO3 crystal was the most proper holographic recording media material among the six crystals studied in the paper. (© 2006 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)  相似文献   

4.
The effect of post treatment on the photorefractive properties of Ru‐doped lithium niobate was studied. The absorption spectra examination of Ru‐doped LiNbO3 crystals with different post treatments showed that the absorption coefficient at 530 nm increased after the reduced treatment was employed and the absorption edge of the reduced crystal shifted towards the infrared band. On the contrary, the trend reversed after the oxidized treatment was employed. In addition, the photorefractive properties were investigated with the two‐beam coupling method conducted via a 532 nm solid state laser. It was found that the oxidized Ru:LiNbO3 had smaller exponential gain coefficient and diffraction efficiency because the charges in the shallow level were exchanged to the deep level. On the other hand, the reduced Ru:LiNbO3 crystals had larger exponential gain coefficient and diffraction efficiency due to the increase of the Ru3+ which existed in the shallow level. The response times of both oxidized and reduced Ru:LiNbO3 were longer than those of the as‐grown ones. (© 2007 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)  相似文献   

5.
Mg:Mn:Fe:LiNbO3 crystals were grown by the Czochralski method. The defect structure was analyzed by UV‐vis spectra and IR spectra. The holographic storage of Mg:Mn:Fe:LiNbO3 crystals was measured by the two color fixed method. The results show that with the increase of MgO doping concentration, the writing time becomes shorter, the dynamic range decreases, photorefractive sensitivity increases and fixing diffraction efficiency decreases. When the MgO doping concentration exceeds 4.5 mol%, the fixing diffraction efficiency approaches zero. The effect of doping Mg ions on the holographic storage properties of Mn:Fe:LiNbO3 crystals is discussed. (© 2008 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)  相似文献   

6.
Congruent LiNbO3:Fe and LiNbO3:Mg,Fe crystals were grown by Czochralski method, and vapor transport equilibration technique was employed to improve the [Li]/[Nb] ratios of these crystals. The influence of stoichiometry and MgO dopant on the photorefractive sensitivity and response time of LiNbO3:Fe crystals was investigated. Both stoichiometry and MgO dopant can effectively reduce the amount of intrinsic defects, but MgO can also decrease the concentration of Fe2+ ions in Li‐sites. Near‐stoichiometric and MgO doped LiNbO3:Fe crystal has high photorefractive sensitivity and fast response time. (© 2006 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)  相似文献   

7.
In:Fe:Cu:LiNbO3 crystals were grown in air by the Czochralski technique with various [Li]/[Nb] ratios of 0.946, 1.050, 1.200, and 1.380 in melt. Based on the ICP‐AES (inductively coupled plasma atomic emission spectrometry) analyzed results, the chemical formula of the triple‐doped In:Fe:Cu:LiNbO3 crystals were obtained. It can be seen that the near‐stoichiometric ratio value is between 1.050 and 1.200 for our samples. The optical damage resistance of In:Fe:Cu:LiNbO3 crystals was characterized by changes in light‐induced birefringence and it increases with the increasing of [Li]/[Nb] ratios. The dependence of the optical damage resistance on the defect structure of In:Fe:Cu:LiNbO3 crystals is discussed in detail based on the obtained chemical formulas. (© 2011 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)  相似文献   

8.
Near‐stoichiometric LiNbO3 single crystal tri‐doped with ZrO2, MnO and Fe2O3 was grown from Li‐riched melt by Czochralski method. The defect structures and composition of these crystals were analyzed by means of ultraviolet‐visible and infrared transmittance spectra. The appearance of 3466 cm‐1 peak in infrared spectra showed that the crystal grown from Li‐riched melt was near stoichiometric. The photorefractive properties at the wavelength of 488 nm and 633 nm were investigated with two‐beam coupling experiment, respectively. The experimental results showed that the response speed and sensitivity were enhanced significantly and the high diffraction efficiency was obtained at 488 nm wavelength. This manifested that near‐stoichiometric LiNbO3:Mn:Fe:Zr crystal was an excellent candidate for holographic storage. (© 2010 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)  相似文献   

9.
本文首次采用Czochralski法生长优质的Scx:Fey:Cuz:LN (x=0,1;, 2;, 3;, 3.5;, y=0.1;, z=0.06;)晶体.测试了晶体抗光致散射能力,以二波耦合光路测试晶体的衍射效率、写入时间和擦除时间,计算光折变灵敏度和动态范围.结果表明:Sc(2mol;):Fe:Cu:LN和Sc(3mol;):Fe:Cu:LN晶体抗光致散射能力比Fe:Cu:LN晶体高两个数量级以上,Scx:Fey:Cuz:LN晶体的写入速度、光折变灵敏度和动态范围等全息存储性能优于Fe:LN晶体.首次采用氪离子激光(482.0 nm,蓝光)作开关光,氦氖激光(632.8 nm,红光)做记录光,以Sc:Fe:Cu:LN晶体作为双光子全息存储记录介质,实现了双光子全息存储固定(非挥发性全息存储).  相似文献   

10.
Hf(2mol%):Fe(0.05wt%):LiNbO3 crystals with various [Li]/[Nb] ratios of 0.94, 1.05, 1.2 and 1.38 have been grown. The photorefractive resistant ability increases with the accretion of [Li]/[Nb] ratio. When the ratio of [Li]/[Nb] is 1.20 or 1.38, the OH absorption band shifts to about 3477cm‐1. The mechanisms of the photorefractive resistant ability increase and the absorption band shift have been discussed. The exponential gain coefficient (Γ) of the crystals was measured with two‐beam coupling method and the effective charge carrier concentration (Neff) was calculated. The results show that Γ and Neff increase with the accretion of [Li]/[Nb] ratio. The temperature effect of codoped Hf:Fe:LiNbO3 crystals was also studied, it was found that the exponential gain coefficient increase dramatically at about 55°C, 70°C and 110°C, this is due to the inner electric field which is resulted from structure phase change. (© 2007 WILEY ‐VCH Verlag GmbH & Co. KGaA, Weinheim)  相似文献   

11.
Zn:Mn:Fe:LiNbO3 crystals were prepared by Czochralski technique. Its microstructure was measured and analyzed by UV‐Vis absorption spectra. The optical damage resistance of Zn:Mn:Fe:LiNbO3 crystals was characterized by the transmitted beam pattern distortion method. It increases remarkably when the concentration of ZnO is over a threshold concentration. Its value in Zn(7.0 mol%):Mn:Fe:LiNbO3 crystal is about three orders of magnitude higher that in the Mn:Fe:LiNbO3 crystal. The dependence of the defects on the optical damage resistance was discussed. The non‐volatile holographic storage was realized in all crystals, and the sensitivity of the Zn(7.0 mol%):Mn:Fe:LiNbO3 crystal is much higher than that of others. (© 2006 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)  相似文献   

12.
A series of Zn:In:Fe:LiNbO3 crystals were prepared by Czochralski method. The crystal composition and defect structure were analyzed by ICP‐OE/MS, UV–vis and IR spectroscopy. The results show that with increasing In3+ doping concentration in melt, the segregation coefficients of both Zn and In ions decrease. The optical damage resistance of Zn:In:Fe:LiNbO3 crystals was studied by the transmitted beam pattern distortion method. It is found that the optical damage resistance of Zn:In(3mol%):Fe LiNbO3 crystals is two orders of magnitude higher than that of Zn:Fe:LiNbO3. (© 2009 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)  相似文献   

13.
Hf:Fe:LiNbO3 crystals were grown in air by the Czochralski technique with various ratios of [Li]/[Nb]=0.94, 1.05, 1.20 in melt. The defect structure and location of doped ions were analyzed by the UV‐visible and infrared spectroscopy. The optical damage resistance ability of Hf:Fe:LiNbO3 crystals was measured by the photo‐induced birefringence change and the transmitted light spot distortion method. The results show that the optical damage resistance ability of Hf:Fe:LiNbO3 crystals is enhanced with the increase of the [Li]/[Nb] ratio. The dependence of the optical damage resistance of Hf:Fe:LiNbO3 crystals on the defect structure is discussed in detail. (© 2010 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)  相似文献   

14.
Hf:Fe:LiNbO3 crystals were grown in air by the Czochralski technique with various [Li]/[Nb] ratios ([Li]/[Nb]=0.94, 1.05, 1.20) in melt. The defect structure and location of doped ions were analyzed by the UV‐visible absorption spectra. The optical damage resistance of Hf:Fe:LiNbO3 crystals was investigated by the photoinduced birefringence change and the transmitted light spot distortion method. The results show that the optical damage resistance ability of Hf:Fe:LiNbO3 crystals decreases with the increase of the [Li]/[Nb] ratio. The dependence of the optical damage resistance of Hf:Fe:LiNbO3 crystals on the defect structure is discussed in detail. (© 2011 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)  相似文献   

15.
Mg:Ce:Fe:LiNbO3 crystals were prepared with fixed concentrations of Fe2O3 and CeO2, and differing concentrations of MgO by the Czochralski technique. Their infrared transmission spectra were measured in order to investigate their defect structures and their optical damage resistance was characterized by the photoinduced birefringence change and transmission facula distortion method. The optical damage resistance of Mg:Ce:Fe:LiNbO3 crystals increases remarkably when the concentration of MgO exceeds a threshold concentration. The dependence of the optical damage resistance on the defect structure of Mg:Ce:Fe:LiNbO3 crystals is discussed in detail. (© 2010 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)  相似文献   

16.
Methods of Raman spectroscopy, laser conoscopy, optical microscopy, and electron spin resonance have been used to study the photorefractive properties and structural and optical homogeneity of the following lithium niobate (LiNbO3) crystals: nominally pure crystals of congruent composition (LiNbO3con); LiNbO3:Cu[0.015 wt %] crystals grown from a melt of congruent composition and nominally pure crystals of stoichiometric composition grown from a melt with 58.6 mol % Li2O (LiNbO3st). A small deformation of optical indicatrix and regular microdomain structures of fractal type are revealed for the LiNbO3:Cu[0.015 wt %]; the microdomain structures may be due to the nonuniform impurity incorporation into the structure. It is shown that oxygen octahedra in the LiNbO3:Cu[0.015 wt %] crystal are deformed in comparison with the octahedra in LiNbO3st and LiNbO3con crystals and that the main and impurity cations are clusterized along the polar axis. It is established that the LiNbO3:Cu[0.015 wt %] crystal exhibits photorefractive properties not only due to the presence of intrinsic defects with localized electrons, as in the case of LiNbO3st, but also due to the charge exchange in copper cations (Cu2+ → Cu+) under illumination.  相似文献   

17.
In:Zn:LiNbO3 crystals doped with different indium concentrations were grown by Czochralski technique. The optical damage threshold value and ultraviolet‐visible absorption spectra of the In:Zn:LiNbO3 crystals were measured. The In:Zn:LiNbO3 crystals were made into optical waveguide substrates using hexanedioic acid as proton exchange agent. The optical damage resistant ability of those optical waveguide substrates was investigated by the m‐line method. The optical damage threshold values of In(2mol.%):Zn(3mol.%):LiNbO3 crystal and optical waveguide substrate are two orders of magnitude higher than those of pure LiNbO3. (© 2007 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)  相似文献   

18.
Near‐stoichiometric Mn:Fe:LiNbO3 crystals doped with various concentration of ZrO2 were grown by top seed solution growth (TSSG) method in the air atmosphere. The Zr concentration in the crystal was determined by inductively coupled plasma optical emission spectrometer. The defect structures were analyzed by means of ultraviolet‐visible and infrared transmittance spectra. The appearance of vibration peak at 3466 cm‐1 in infrared spectra manifested that Li/Nb ratio in crystals approached to stoichiometric proportion. The fundamental absorption edge represented continuous red‐shift which was discrepancy with congruent doped LiNbO3 crystals showed that doping ions possessed different location mechanism. The light‐induced scattering of the doped stoichiometric LiNbO3crystals were quantitatively scaled via incident exposure energy. The results demonstrated that Zr(2 mol%):Mn:Fe:LiNbO3 crystal had the weakest light‐induced scattering and the mechanism related to their defect structures was discussed. (© 2012 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)  相似文献   

19.
The pure congruent LiNbO3, Er:LiNbO3 and Zn,Er co‐doped Li‐rich LiNbO3 crystals were grown by Czochralski method. The X‐ray diffraction method and ultraviolet‐visible absorption spectra of the crystals were used to analyze the structure of the crystals. The photo‐damage ability resistance of the crystals was measured. The Zn,Er co‐doped Li‐rich LiNbO3 crystals show a decrease in lattice constant values, a shift in absorption edge of ultraviolet‐visible absorption spectra towards shorter wavelength, and three orders of magnitude increase in photo‐damage resistance compared to congruent LiNbO3 crystal. The intrinsic and extrinsic defects are discussed to explain the enhance of the photo‐damage ability resistance  相似文献   

20.
Influence of defect structure on the infrared transmission spectra of OH in Zn:Fe:LiNbO3 crystals with various ZnO concentration and different Li/Nb ratios was investigated. It indicates that above the Zn concentration threshold the OH absorptions bands successively shift from 3482cm‐1 to 3504cm‐1 and 3529cm‐1. The intensity of the 3504cm‐1 band increases with ZnO concentration increasing. The optical damage resistance of the Zn:Fe:LiNbO3 crystals increases rapidly when the ZnO concentration exceeds a threshold value. This result contributed to the site alteration from the Li sites to Nb sites due to Zn‐doping in crystal. © 2006 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim  相似文献   

设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号