964 resultados para Nd^3 :GGG


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用提拉法生长了掺铬、钕的钆镓石榴石(Cr^4+,Nd^3+:GGG)自调Q激光品体。报道了室温下的吸收光谱和荧光光谱特性。分析了Cr离子浓度对光谱性质的影响。比较了Cr^4+:GGG,Nd^3+:GGG和(Cr^4+,Nd^3+):GGG晶体吸收光谱的关系。测量了(Cr^4+,Nd^3+):GGG晶体和Nd^3+:GGG晶体的荧光寿命,它们分别是33μs和250μs。实验表明,(Cr^4+,Nd^3+):GGG晶体是一种非常有潜力的自调Q激光晶体,可以实现大功率激光器的小型化和全固态化。

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用提拉法生长了掺铬、钕的钆镓石榴石(Cr^4+,Nd^3+:GGG)晶体,研究了室温下的吸收光谱和荧光光谱性质,以及晶体中Cr离子浓度对Nd离子光谱性质的影响。应用Judd—ofelt理论计算了强度参数Ωt(t=2,4,6),自发辐射跃迁几率、荧光分支比和辐射辱命等光谱参数。应用McCumber理论计算^4F3/2→^4I11/2能级跃迁的受激发射截面。结果表明:Cr^3+在300~900nm之间较强地增加了吸收截面,尤其是伴随Cr^3+→Nd^3+有效的能量转移。Cr^4+在1.06μm附近的吸收减弱了

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将SiO2含量超过97wt%的具有纳米级微孔的多孔高硅氧玻璃浸泡在含有Nd^3+离子的溶液后取出,在1100℃烧结成透明无孔高硅氧玻璃。在800nm的激光抽运下,这种Nd^3+离子掺杂的高硅氧玻璃微片激光器实现了斜率效率为62%,光-光转换效率为42%,波长为1064nm的激光输出。

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采用传统无压烧结工艺制备Nd^3 +掺杂的氧化镧钇透明激光陶瓷,测试了其吸收和荧光光谱.采用Judd-Ofelt理论对Nd^3 +掺杂量为1 .5at %的样品光谱参量进行了计算.根据吸收光谱,拟合得到三个强度参量分别为:Ω2=6 .57×10^-20cm^2,Ω4=2 .04×10^-20cm^2,Ω6=4 .38×10^-20cm^2.根据这三个参量计算了样品的辐射寿命,跃迁几率,荧光分支比,量子效率和品质因子,并对结果作了分析.

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于2010-11-23批量导入

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采用两步加热高温固相法合成了掺杂Nd3+的LiFe1-xNdxPO4/C复合材料(x=0,0.01,0.02,0.04,0.06,0.08)。用TG-DSC对前驱体进行分析和SQUID(超导量子干涉仪)对样品中Fe3+的磁性测定,优化了合成工艺条件;采用XRD、FE-SEM、EDS等方法分析了样品的结构并对其电化学性能进行了测试。结果表明:LiFe1-xNdxPO4/C复合材料具有橄榄石型结构;当Nd3+的掺杂量6%(物质的量分数)、煅烧温度700℃、煅烧时间16 h时,样品在0.2C(1C=170.0 mA.g-1)电流密度下的最大放电比容量可达165.2 mAh.g-1,循环100次后的容量保持率仍为92.8%,在1C、2C、5C下的最大放电比容量分别为146.8、125.7和114.8 mAh.g-1。通过测定样品在不同较低倍率下的放电比容量,采用外推法得出制备样品的实测理论比容量为168.7 mAh.g-1。

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利用研究复杂晶体化学键的理论方法,计算了一组ABO4型基质晶体的结构参数和化学键参数,发现Nd3+离子的总晶场劈裂能ΔE与晶体的平均共价性有线性关系.

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用循环伏安法和恒电流电解后的电位时间曲线法,研究了LiClKCl熔体中Nd3+和Ho3+在Mo电极上的电化学行为。结果表明,Nd3+和Ho3+在Mo电极上的还原都为一步3电子可逆过程。其扩散系数分别为:113×10-6和2142×10-5cm2·s-1(450℃),450℃下Ho3+/Ho电极对的标准氧化还原电位为2987V(vs·Cl/Cl-1),并讨论了实验值较理论值偏负的原因。

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本文利用循环V-A法(CV)研究了Nd~(3+)在液体Ga电极上还原的电化学反应动力学。结果表明,Nd~(3+)在Ga电极上的还原是分步进行的。第一步在较高的电位扫描速度下为扩散控制的可逆电荷传递反应,即Nd~(3+)+e?Nd~(2+);在电位扫描速度较低时,随后的化学反应为第一步反应的控制步骤,即Nd~(3+)+e?快Nd~(2+)+mCl→慢NdCl_m~(2-m)。第二步为不可逆的电荷传递反应,即沉积的金属Nd与Ga合金化,Nd~(2+)+2e→Nd(Ga)。估算了该反应的标准反应速度常数为7.0×10~(-3)cm/s。

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Neodymium based fluorescence presents several advantages in comparison to conventional rare earth or enzyme-substrate based fluorescence emitting sources (e.g.Tb, HRP). Based on this fact we have herein explored a Nd-based fluoroimmunoassay. We efficiently detected the presence of an oxidized low-density lipoprotein (oxLDL) in human plasma a well-known marker for cardiovascular diseases, which causes around 30% of deaths worldwide. Conventional fluoroimmunoassay uses time-resolved luminescence techniques, with detection in the visible range, to eliminate the fluorescence background from the biological specimens. By using an immunoassay based on functionalized Y(2)O(3):Nd(3+) nanoparticles, where the excitation and emission processes in the Nd(3+) ion occur in the near-infrared (NIR) region, we have succeeded in eliminating the interferences from the biological fluorescence background, avoiding the use of time-resolved techniques. This yields higher emission intensity from the Nd(3+)-nanolabels and efficient detection of anti-oxidized low-density lipoproteins (anti-oxLDL) by Y(2)O(3):Nd(3+)-antibody-antigen conjugation, leading to a novel biolabeling method. (C) 2010 Elsevier B.V. All rights reserved.

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The effect of the sintering method on the microstructural and electrical properties of (Pb(0.89)Nd(0.02)La(0.09))(Zr(0.65)Ti(0.35))O(3) (PNLZT) ceramics was studied by impedance spectroscopy. Structural and microstructural analyses were performed using x-ray and scanning electron microscopy techniques. Two different sintering routes were employed: the conventional and the hot-pressing sintering methods. The impedance analysis provided a convincing evidence for the existence of both grain (g) and grain boundary (gb) contributions to the conduction process. An equivalent circuit for the impedance behaviour has been proposed and discussed. The variation in the sintering method produces significant changes in the grain and grain boundary conductivities. For the grain effect, the main conduction mechanism has been associated with oxygen vacancy migration. Otherwise, for grain boundary conductivity the impedance behaviour has been discussed in terms of the brick-layer and the constriction resistance models (BLM and CRM, respectively).

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In rare earth ion doped solids, a resonant non-linear refractive index, n2, appears when the laser pumps one of the ion excited states and the refractive index change is proportional to the excited state population. In these solids there are usually thermal and non-thermal lensing effects, where the non-thermal one is due to the polarizability difference, Δα, between excited and ground states of the ions. We have used the time resolved Z-scan and a mode-mismatched thermal lens technique with an Ar+ ion laser in Er+3 (20ZnF2-20SrF2-2NaF-16BaF2-6GaF3-(36 - x)InF3-xErF3, with x= 1, 2, 3 and 4 mol%) and Nd+3 (20SrF2-16BaF2-20ZnF2-2GdF3-2NaF-(40 - x)InF3-xNdF3, with x = 0.1, 0.25, 0.5-1 mol%) doped fluoroindate glasses. In both samples we found that the non-linear refraction is due to the thermal effect, while the non-thermal effect is negligible. This result indicates that in fluoride glasses Δα is very small (less than 10-26 cm3). We also measured the imaginary part of the non-linear refractive index (n″2) due to absorption saturation.

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We investigated near-infrared-to-blue upconversion from thulium (Tm 3+) doped in tellurite glasses upon continuous wave excitation near 800 nm. We observed an enhancement of over two orders of magnitude of the upconverted emission at ∼480nm when neodymium (Nd 3+) ions were codoped with Tm 3+ ions. For comparison, using a Tm 3+:Nd 3+ codoped fluorozirconate glass as a reference material we observed a 40-fold enhancement of the blue emission. Analysis of the blue emission for samples with different doping levels of Nd 3+ ions showed that energy transfer between Nd 3+ and Tm 3+ is the mechanism responsible for the enhancement in upconversion. © 2002 American Institute of Physics. © 2002 American Institute of Physics.

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An upconversion random laser (RL) operating in the ultraviolet is reported for Nd 3+ doped fluoroindate glass powder pumped at 575 nm. The RL is obtained by the resonant excitation of the Nd 3+ state 2G 7/2 followed by energy transfer among two excited ions such that one ion in the pair decays to a lower energy state and the other is promoted to state 4D 7/2 from where it decays emitting light at 381 nm. The RL threshold of 30 kW/cm 2 was determined by monitoring the photoluminescence intensity as a function of the pump laser intensity. The RL pulses have time duration of 29 ns that is 50 times smaller than the decay time of the upconversion signal when the sample is pumped with intensities below the RL laser threshold. © 2011 Optical Society of America.