Mg2+对Fe:LiNbO3晶体光折变响应时间的影响

在Fe:LiNbO₃中掺进3mol%和6mol%MgO,生长了Mg:Fe:LiNbO₃晶体.测试了Mg:Fe:LiNbO₃晶体抗光致散射能力、衍射效率、响应时间和光电导.推导响应时间与光电导之间的关系.在Fe:LiNbO₃晶体中掺进6mol%的Mg²⁺,它的抗光致散射能力比Fe:LiNbO₃晶体提高一个数量级,响应速度比Fe:LiNbO₃晶体提高四倍.     

掺锌LiNbO3晶体的生长及其光学性能

在LiNbO₃中掺进3mol%、5mol%、7mol%ZnO生长Zn:LiNbO₃晶体.测试Zn:LiNbO₃晶体的吸收光谱,研究Zn:LiNbO₃晶体吸收边紫移的机制.测试Zn:LiNbO₃晶体的红外光谱,研究Zn(7mol%):LiNbO₃晶体OH 吸收峰由3484cm^-1移到3530cm^-1的机制.测试Zn:LiNbO₃晶体倍频转换效率和相位匹配温度,研究Zn:LiNbO₃晶体倍频转换效率增强的机制.     

Mg∶Fe∶LiNbO_3晶体的生长及光学性能研究

在Fe∶LiNbO3中掺进MgO和Fe2 O3以提拉技术生长Mg∶Fe∶LiNbO3晶体 对晶体进行极化和还原处理 测试晶体的吸收光谱 ,Mg∶Fe∶LiNbO3晶体吸收边相对Fe∶LiNbO3晶体发生紫移 测试晶体的红外光谱 ,Mg∶(5mol % )Fe∶LiNbO3晶体OH 吸收峰由Fe∶LiNbO3晶体的 3482cm- 1移到35 34cm- 1 采用锂空位模型阐述Mg∶Fe∶LiNbO3晶体 ,吸收边和OH- 吸收峰移动的机理 测试晶体的抗光致散射能力 Mg∶(5mol% )Fe∶LiNbO3晶体抗光致散射能力比Fe∶LiNbO3晶体提高一个数量级以上 测试晶体的衍射效率和响应时间 Mg∶Fe∶LiNbO3晶体响应速度比Fe∶LiNbO3晶体提高四倍     

In∶Nd∶LiNbO3晶体倍频性能的研究

在 LiNbO₃中掺进In₂O₃和Nd₂O₃, 以Czochralski技术生长了In∶Nd∶LiNO₃晶体. 通过光斑畸变法测得In∶Nd∶LiNbO₃晶体的光损伤阈值为1.98×104 W/cm², 比Nd∶LiNbO₃晶体的1.6×102 W/cm²高两个数量级以上;晶体吸收光谱的测试表明, In∶Nd∶LiNbO₃晶体的吸收边相对Nd∶LiNbO₃晶体发生紫移. 研究了In∶Nd∶LiNbO₃晶体的倍频性能, 结果表明, In∶Nd∶LiNbO₃晶体的相位匹配温度在室温附近, 倍频转换效率比Nd∶LiNbO₃晶体提高二倍.     

Mg2+对Fe∶LiNbO3晶体光折变响应时间的影响

在 Fe∶Li Nb O3 中掺进 3 mol%和 6mol% Mg O,生长了 Mg∶Fe∶L i Nb O3 晶体 .测试了 Mg∶Fe∶Li Nb O3 晶体抗光致散射能力、衍射效率、响应时间和光电导 .推导响应时间与光电导之间的关系 .在 Fe∶Li Nb O3 晶体中掺进 6mol%的 Mg2 + ,它的抗光致散射能力比Fe∶L i Nb O3 晶体提高一个数量级 ,响应速度比 Fe∶Li Nb O3 晶体提高四倍     

Zn:Fe:LiNbO3晶体全息存储性能研究

以提拉法生长Zn(1mol%):Fe:LiNbO3, Zn(4mol%):Fe:LiNbO3,Zn(7mol%):Fe:LiNbO3晶体.Zn:Fe:LiNbO3晶体随着Zn2+浓度的增加,抗光致散射能力增加,Zn(7mol%):Fe:LiNbO3晶体抗光致散射能力比Fe:LiNbO3晶体提高两个数量级以上.测试了Zn:Fe:LiNbO3晶体衍射效率、响应时间.以Zn(7mol%):Fe:LiNbO3晶体作为存储元件,Zn(4mol%):Fe:LiNbO3晶体作为位相共轭镜,进行全息关联存储试验.试验结果显示出成像质量好、图像清晰完整、噪音小等优点.研究了Zn:Fe:LiNbO3晶体全息存储性能增强的机理.Zn(4mol%):Fe:LiNbO3晶体具有全息存储性能最佳的综合指标.     

m线法研究掺杂LiNbO3晶体波导基片的光损伤

采用m线法研究了掺杂LiNbO₃晶体波导基片的光损伤,发现抗光损伤能力依次为Mg:LiNbO₃、LiNbO₃、Fe:LiNbO₃(氧化),Fe:LiNbO₃(还原).对于同样材料,质子交换光波导的抗光损伤能力高于钛扩散光波导。     

掺镁铌酸锂晶体抗光损伤机理的研究

通过测试Mg(5mol%):LiNbO₃、Mg(4m0l%):LiNbO₃和LiNbO₃等晶体的光损伤阈值、红外透射光谱、倍频性能等,研究了Mg²⁺在Mg:LiNbO₃晶体中所处的状态以及高掺镁抗光损伤能力增强的机理。     

Tb、Fe双掺LiNbO3晶体的生长及其光折变效应的研究

用提拉法从熔体中生长出Tb、Fe双掺LiNbO₃晶体,用二波耦合方法测试了晶体的指数增益系数、衍射效率和响应时间。Tb:Fe:LiNbO₃薄晶片中,由于光爬行作用,使得晶体的指数增益系数和衍射效率大大增强,掺入Tb后晶体的光电导值增大,响应时间缩短。     

Ce:Co:LiNbO3晶体光折变性能研究

在LiNbO₃中掺进CeO₂和Co₃O₄,以Czchralski技术首次生长Ce:Co:LiNO₃, Ce:LiNbO₃, Co:LiNbO₃晶体.通过测试Ce:LiNbO₃, Co:LiNbO₃和Ce:Co:LiNbO₃晶体的指数增益系数, 位相共轭反射率和响应时间,计算晶体的有效载流子浓度和光电导.Ce离子能提高LiNbO₃晶体光折变灵敏度,Co离子能提高LiNbO₃晶体的响应速度和抗光致散射能力,从而Ce:Co:LiNbO₃晶体具有较高的指数增益系数,位相共轭反射率,响应速度.Ce:Co:LiNbO₃晶体具有优良的光折变性能.     

Preparation and holographic storage properties of tri-doped Mg:Mn:Fe:LiNbO3 crystals

Doping MgO, MnO and Fe₂O₃ in LiNbO₃ crystals, tri-doped Mg:Mn:Fe:LiNbO₃ single crystals were prepared by the conventional Czochralski method. The UV-vis absorption spectra were measured and the shift mechanism of absorption edge was also investigated in this paper. In Mg:Mn:Fe:LiNbO₃ crystal, Mn and Fe locate at the deep level and the shallow level, respectively. The two-photon holographic storage is realized in Mg:Mn:Fe:LiNbO₃ crystals by using He-Ne laser as the light source and ultraviolet as the gating light. The results indicated that the recording time can be significantly reduced for introducing Mg²⁺ in the Mg:Mn:Fe:LiNbO₃ crystal.     

The effect of In doping on optical properties of Fe:LiNBO3 crystals

Fe:LiNbO₃ and In:Fe:LiNbO₃ crystals were grown by Czochralski method. The absorption spectra were measured to investigate their defect structure. The photo damage resistance and photorefractive properties were measured. The photo damage resistance of the In:Fe:LiNbO₃ crystal in which the In concentration is above the threshold value is one order of magnitude higher than that of the Fe:LiNbO₃ crystal. The mechanisms of the violet shift of the absorption edge and the enhancement of the photorefractive effect of In:Fe:LiNbO₃ crystals were investigated.     

Growth and photorefractive properties of near-stoichiometric In:Fe:Cu:LiNbO3 crystals

The near-stoichiometric LiNbO₃ crystal co-doped with In₂O₃, Fe₂O₃, and CuO has been grown from a Li-rich melt (Li/Nb = 1.38, atomic ratio) by the Czochralski method in air atmosphere for the first time. The OH⁻ absorption spectra were characterized to investigate the structure defects of the crystals. The appearance of the 3506 cm⁻¹ absorption peak manifests that the composition of the grown crystal is close to the stoichiometric ratio. The photorefractive properties were also measured by the two-wave coupling experiments. The results show that the near-stoichiometric In:Fe:Cu:LiNbO₃ crystal has a larger refractive index change, higher recording sensitivity and larger two-wave coupling gain coefficient than those obtained in the congruent In:Fe:Cu:LiNbO₃ crystal under the same experimental conditions. The material of near-stoichiometric In:Fe:Cu:LiNbO₃ crystal is a promising candidate for blue photorefractive holographic recording.     

Enhancement of blue holographic properties in Zr4+-doped near stoichiometric Fe:LiNbO3 crystals

The near stoichiometric LiNbO₃ crystals co-doped with ZrO₂ and Fe₂O₃ have been grown from a Li-rich melt (Li/Nb=1.38, atomic ratio) by the Czochralski method in air atmosphere at the first time. The OH^? absorption and UV–vis absorption spectra were characterized to investigate the defect structure of the crystals. The appearances of the 3479 cm^?1 absorption peak and 358 nm absorption edge manifest that the composition of the grown crystal is close to the stoichiometric ratio. The blue holographic properties were also measured by the two-wave coupling experiments. As a result, in the near stoichiometric Zr:Fe:LiNbO₃ crystals, photorefractive response speed, recording sensitivity, and two-wave coupling gain coefficient are significantly enhanced. Meanwhile, the high saturation diffraction efficiency is still maintained. These findings prove that the material of near stoichiometric Zr:Fe:LiNbO₃ crystals are a promising candidate for blue photorefractive holographic recording.     

Studies of absorption spectra and the photovoltaic effect in LiNbO3:Mg:Fe crystals

The absorption spectra, photoconductivities and photovoltaic currents of LiNbO₃:Fe crystals with different Mg doping levels and Li/Nb ratios in the oxidized state have been investigated at room temperature. The Fe²⁺ ions in LiNbO₃:Mg:Fe with Mg content above a critical value are more easily oxidized than in crystals with Mg content below a critical value. The photoconductivity of LiNbO₃:Mg:Fe crystals with Mg content above a critical value is one order of magnitude higher than those with Mg content below a critical value, however, the photovoltaic current of the former is one order of magnitude lower than the latter. The differences are postulated to be due to different sites of Fe in these two classes of crystals.     

Mg2+对Ce:Fe:LiNbO3晶体光折变性能的作用和影响

在Ce(0.1wt%):Fe(0.08wt%):LN中掺进摩尔分数为（0.2%,0.4%,0.6%）的MgO,采用提拉法生长Mg:Ce:Fe:LN晶体.测试晶体的吸收光谱,Mg:Ce:Fe:LN晶体的吸收边相对Ce:Fe:LiNbO3晶体发生紫移,Mg(6%):Ce:Fe:LN晶体OH－吸收峰移到3 532 cm－1,研究OH－吸收峰移动机理.以二波耦合光路测试Mg:Ce:Fe:LN晶体的指数增益系数和响应时间,发现Mg:Ce:Fe:LN晶片厚度减小时指数增益系数显著增加.首次采用光爬行效应解释指数增益系数增加机理.     

OH-吸收带作为铌酸锂晶体缺陷结构的探针

本文报道了一组不同Li/Nb比和另一组不同掺Mg浓度的LiNbO₃晶体室温OH^-吸收带的实验结果,观察到OH^-吸收带的三峰结构及其随Li/Nb比的变化,以及重掺Mg晶体中(6mol％MgO)OH^-吸收带转变为双峰结构,并向高能端移动54cm^-1。根据LiNbO₃的晶体结构以及Abrahams和Smyth的缺陷结构模型,对化学计量晶体、一致熔化晶体和掺Mg晶体分别进行讨论。并提出重掺Mg晶体中OH^-吸收带向高能端的移动可能是由于当掺Mg浓度超过阈值后Mg²⁺离子开始进入Nb位而引起的。 关键词：