159 resultados para fluoride varnish
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利用漫反射率、X射线光电能谱和质谱等测量方法,研究了固态和气态四氧化二氮(N2O4)对漫反射试片氟化镁(MgF2)涂层表面的污染情况.实验表明,固态N2O4对MgF2涂层有严重侵蚀作用,N2O4固粒污染后的涂层表面漫反射率下降了20%~30%.在一定的时间内,气态N2O4对涂层表面的影响显著地依赖它的压力.试片在压力为6.9×104 Pa和200Pa的N2O4蒸气中分别放置10 min,前者厚度为40μm的MgF2涂层基本消失,表面漫反射率下降约20%;后者涂层表面的原子组成和漫反射率变化很小.还给出了MgF2涂层表面N2O4分子吸附摩尔密度,以及与涂层表面碰撞的N2O4分子通过化学吸附过程提取MgF2的几率.
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研究了超短脉冲激光照射下LiF晶体的破坏机理及其超快动力学过程,利用扫描电镜和原子力显微镜等测试手段,观测了飞秒激光照射下LiF晶体的烧蚀形貌。利用烧蚀面积与激光脉冲能量的对数关系确定了LiF晶体的破坏阈值,并利用非线性玻璃棒展宽脉宽,得到了800nm激光作用下LiF破坏阈值对激光脉宽(50~1000fs)的依赖关系;利用抽运一探针超快探测平台,探测了LiF烧蚀过程中反射率的变化。采用雪崩击穿模型,并根据晶体材料反射率与材料的介电常量的依赖关系,通过数值计算,模拟了材料烧蚀阈值与脉宽的依赖关系及材料激发过
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用扫描电镜(SEM)研究了氟化镁在800nm超短脉冲激光作用下的单枪表面烧蚀形貌.根据烧蚀斑面积与激光脉冲能量间的对数关系,测得烧蚀阈值与激光脉宽的关系曲线(55—750fs).计算了导带电子的双光子吸收,改进了多速率方程模型.很好地解释了实验结果.
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Fluorescence of Tm3+/Er3+ codoped bismuth-silica (BS) glasses and the sensitization of Ce3+ are investigated. It shows that Ce3+ codoping with Tm3+/Er3+ in BS glasses results in a quenching of Tm3+ ion emission from F-3(4) to the H-3(6) level. Consequently, the 1.47 mu m emission occurs after the population inversion between the H-3(4) and F-3(4) levels. Furthermore, the codoped glasses show the broad emission spectra over the whole S and C bands with full-width at half-maximum (FWHM) up to about 119nm, as it combines 1.55 mu m emission band of Er3+ with 1.47 mu m emission band of Tm3+ under 800nm excitation.
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在摩尔分数组成x(BaO),r(Ga2O),r(GeO2)为0.20,0.15,0.65的玻璃中,分别以摩尔分数0.05,0.10.0.15和0.20的BaF2替代BaO,研究了氟化物对玻璃折射率和光吸收性质的影响。结果表明,在玻璃中加入氟化物.玻璃折射率和色散降低,玻璃的紫外吸收边向短波侧迁移,而红外吸收边无明显变化。不含氟化物的氧化物玻璃中含有大量的OH基.这些OH基在2.24μm、2.97μm和4.23μm附近引起光吸收.在含氟化物的玻璃中,2.24μm的吸收峰消失,而2.97μm和4.23μm附近
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以摩尔组成为8.7MgF2-17.4CaF2-8.7SrF2-13.3BaF2-13.0YF3-31.6.AlF3-7.3ZrF4的氟化物玻璃为对象,研究了玻璃的分相和析晶.研究表明,玻璃中同时含有AlF3和ZrF4时,玻璃产生明显的分相,玻璃在高温下对水比较敏感,容易产生表面析晶.玻璃内部的析晶主要来自稳定性较差的富Al相,受空气中水分的影响,玻璃表面的析晶首先产生于富Zr相.依据玻璃的分相和析晶表现,讨论了含AlF3和ZrF4氟化物玻璃的表面析晶机理.
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研究了掺铒氟(卤)磷碲酸盐玻璃的吸收光谱和上转换荧光光谱,探讨了Er^2+在氟(卤)磷碲酸盐玻璃中的上转换发光机理.在975nm激光二极管抽运下产生强烈的上转换红光及绿光。且红光的发光强度要远远大于绿光.以PbCl2取代PbF2后,红光的发光强度下降,而绿光却没有明显变化;以ZnCl2取代ZnF2达5mol%时,红光和绿光的发光强度均明显增大.
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探求新的具有优良的热学和光学性能的基质玻璃系统,是获得具有宽带宽和增益平坦的掺Er^3+光纤放大器(EDFA)的一种有效途径。制备了一种新型氧氟碲酸盐玻璃TeO2-BaF2-LaF3,并对其热学性能和光学性质进行了测试。应用乍得-奥菲尔特(Judd-Ofelt)理论计算了Er^3+离子的J-O理论参量和荧光寿命r。探讨了氟化物的引入对碲酸盐玻璃结构的改变的影响,并分析了其对玻璃的热学性质和光学性质的影响。实验发现,获得的氧氟碲酸盐玻璃具有优良的热学稳定性(△T=156.6C),宽的荧光半峰全宽(72nm)
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锗酸盐和氟铝酸盐透红外玻璃材料作为窗口或头罩材料具有广泛的应用前景。结合锗酸盐玻璃含有少量水的问题,在成分中引入氟化物,实验表明:随氟化物含量增加.玻璃中羟基含量逐渐降低。同时通过对熔制温度的调整,获得了不合羟基的红外玻璃。针对氟铝酸盐玻璃在冷却过程中易析晶的问题,在氟化物组分中加入少量重金属氧化物TeO2,得到析晶性能好的氧氟铝酸盐玻璃。同时给出了两类红外材料的一些物理、化学性质。
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Optical spectroscopic properties of Er3+-doped alkaline-earth metal modified fluoropho sphate glasses have been investigated experimentally for developing broadband fiber and planar amplifiers. The results show a strong correlation between the alkaline-earth metal content and the spectroscopic parameters such as absorption and emission cross sections, full widths at half-maximum and Judd-Ofelt intensity parameters. It is found that strontium ions could have more influences on the Judd-Ofelt intensity parameters and the absorption and emission cross sections than other alkaline-earth metal ions such as Mg2+, Ca2+, Ba2+. The sample containing 23 mol% strontium fluoride exhibits the maximum emission cross section of 7.58 x 10(-21) cm(2), the broadest full width at half-maximum of 65 nm and the longer lifetime of 8.6 ms among the alkaline-earth metal modified fluorophosphates glasses studied. The Judd-Ofelt intensity parameter Omega(6)s, the emission cross sections and the full widths at half-maximum in the Er3+-doped fluorophosphate glasses studied are larger than in the silicate and phosphate glasses.
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在氟铝酸盐玻璃组分中加入适量声子能量低的重金属氧化物TeO2,得到一种新的氧氟化物玻璃。该材料具有良好的成玻璃性能,适合制作大尺寸红外窗口镜。研究了TeO2含量对玻璃特征温度、阿贝数和红外透过性能的影响。同时测试了这种玻璃的抗DF激光能力,结果表明:TeO2含量为15%的玻璃,DF激光破坏阈值达14.95kW·cm^-2。分析显示,由于玻璃基质的多声子吸收,对激光能量的吸收而引起的热冲击是导致玻璃破坏的主要原因。进一步降低玻璃中水分,可以提高玻璃抗激光破坏性能。
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研究了掺铒TeO2-ZnO-PbCl2碲酸盐基氧卤玻璃在977nm激光二极管抽运下的发光和上转换发光特性,结果发现除红外1.53μm^4I13.2→^4I15/2发光外(荧光半高宽高达69nm),该玻璃还存在很强的^2H11/2→^4I15/2(527nm),^4S3/2→^4I15/2(549nm)和^4R9/2→^4I15/2(666nm)可见上转换发光.应用Judd-Ofelt理论计算得到玻璃强度参数Ω1(t=2,4,6)分别为Ω2=5.87×10^20cm^2,Ω4=2.08×10^2-cm^2,
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Er3+:Yb3+ codoped tellurite-fluorophosphate (TFP) glass ceramic exhibits much stronger upconversion luminescence. The intensity of the 540 nm green light and 651 nm red light of the TFP glass ceramic is 120 times and 44 times stronger than that of the fluorophospahte (FP) glass, respectively. XRD analysis shows that the nanocrystal in TFP glass ceramic is SrTe5O11. TFP glass ceramic also displays much higher upconversion fluorescence lifetime and crystallization stability. The narrow and strong peak at 540 nm is very ideal for practical upconversion luminescence realization. This work is a new trial for exploring non-PbF2 involved nanocrystal upconversion glass ceramics.
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Er3+ doped multicomponent fluoride based glass was prepared. These precursor fluoride glass samples were then heated using different schedules. Crystalline phase particles were successfully precipitated in the multicomponent fluoride glass samples after heat treatment. The influence of heat treatment on the spectroscopic properties of Er3+ in multicomponent fluoride based glass samples were discussed. Small changes of the Judd-Ofelt parameters Omega(i) (i = 2,4,6) were found in multicomponent fluoride glass samples before and after heat treatment compared to oxyfluoride telluride glass. Preparation conditions used to produce transparent multicomponent fluoride glass ceramics doped with rare-earth ions are discussed. (c) 2007 Elsevier B.V. All rights reserved.
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We demonstrate broadband optical amplification at 1.3 mu m in silicate glass-ceramics containing beta-Ga2O3:Ni2+ nanocrystals with 980 nm excitation for the first time. The optical gain efficiency is calculated to be about 0.283 cm(-1) when the excitation power is 1.12 W. The optical gain shows similar wavelength dependence to luminescence properties. (C) 2007 Optical Society of America.