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Chemical Vapour Deposition for Optical Fibre Technology 光纤技术中的化学气相沉积
Pub Date : 1995-06-01 DOI: 10.1051/JPHYSCOL:19955115
L. Cognolato
At the beginning of the seventies, a break-through took place in the telecommunication research. The introduction of Chemical Vapour Deposition technology in the manufacture of optical fibres allowed both technical quality and economical convenience to realise optical networks, thus beginning the telecommunication revolution. Since that moment, a great development of the CVD techniques has been performed, introducing several methods to produce fibres with geometry and optical properties optimised for different applications. An overview of the different methods is given, and the problems which have been to be solved in these years are described.
七十年代初,电信研究取得了突破性进展。化学气相沉积技术在光纤制造中的引入,使得实现光网络在技术质量和经济上都很方便,从而开始了电信革命。从那时起,CVD技术有了很大的发展,引入了几种方法来生产具有不同应用优化的几何和光学特性的纤维。对不同的方法进行了概述,并对近年来需要解决的问题进行了描述。
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引用次数: 25
Growth of (YBaCuO)m/(PrBaCuO)n Superlattices by MOCVD MOCVD法生长(YBaCuO)m/(PrBaCuO)n超晶格
Pub Date : 1995-06-01 DOI: 10.1051/JPHYSCOL:1995549
N. Didier, B. Chenevier, O. Thomas, J. Sénateur, F. Weiss, A. Gaskov
[(YBaCuO) m /(PrBaCuO) n ] 10 multilayers have been deposited by Metal Organic Chemical Vapor Deposition (MOCVD). The films grow on SrTiO 3 (100) and MgO (100) substrates and have c-axis perpendicular to the substrate. A serie of superlattices has been synthesised with different deposition temperatures ranging between 700 and 850°C with different modulations (the thickness of YBCO layers staying unchanged and equal to 100A). The elements concentrations profiles at the interfaces and the interdiffusion were determined by secondary neutral mass spectroscopy (SNMS). X-ray diffraction show satellite peaks (characteristic of superlattice modulation) around 001 and 002 reflections. Moreover, the samples show a good in-plane orientation. The superconducting properties are analysed by AC screening. The critical temperature reaches 88K in the case of m=8 and n=2 (n and m being the numbers of units cells along c-axis for YBCO layer and PBCO one respectively).
采用金属有机化学气相沉积(MOCVD)技术沉积了[(YBaCuO) m /(PrBaCuO) n] 10多层膜。薄膜生长在srtio3(100)和MgO(100)衬底上,其c轴垂直于衬底。在不同的沉积温度(700 ~ 850℃)和不同的调制下合成了一系列的超晶格(YBCO层的厚度保持不变,等于100A)。用二次中性质谱(SNMS)测定了界面和相互扩散处的元素浓度谱。x射线衍射在001和002反射附近显示卫星峰(超晶格调制的特征)。此外,样品具有良好的面内取向。用交流筛选法对其超导性能进行了分析。当m=8和n=2 (n和m分别为YBCO层和PBCO层沿c轴的单位胞数)时,临界温度达到88K。
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引用次数: 0
Preparation of YBCO on YSZ Layers Deposited on Silicon and Sapphire by MOCVD : Influence of the Intermediate Layer on the Quality of the Superconducting Film 在硅和蓝宝石表面沉积YSZ层上MOCVD制备YBCO:中间层对超导膜质量的影响
Pub Date : 1995-06-01 DOI: 10.1051/JPHYSCOL:1995551
G. Garcia, J. Casado, J. Llibre, M. Doudkowski, J. Santiso, A. Figueras, S. Schamm, D. Dorignac, C. Grigis, M. Aguiló
YSZ buffer layers were deposited on silicon and sapphire by MOCVD. The layers deposited on silicon were highly oriented along [100] direction without in-plane orientation, probably because the existence of the SiO2 amorphous interlayer. In contrast, epitaxial YSZ was obtained on (1-102) sapphire showing an inplane texture defined by the following relationships : (100) YSZ // (1-102) sapphire and (110) YSZ // (01-12) sapphire. Subsequently, YBCO films were deposited on YSZ by MOCVD. Structural, morphological and electrical characterization of the superconducting layers were correlated with the in-plane texture of the buffer layers.
利用MOCVD技术在硅和蓝宝石表面沉积了YSZ缓冲层。沉积在硅上的层沿[100]方向取向高,无面内取向,可能是由于SiO2非晶夹层的存在。相反,在(1-102)蓝宝石上获得外延YSZ,显示出由以下关系定义的面内纹理:(100)YSZ //(1-102)蓝宝石和(110)YSZ //(01-12)蓝宝石。随后,利用MOCVD在YSZ表面沉积YBCO薄膜。超导层的结构、形态和电学特性与缓冲层的面内织构有关。
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引用次数: 2
Atomic Layer Epitaxy Growth of AIN Thin Films AIN薄膜的原子层外延生长
Pub Date : 1995-06-01 DOI: 10.1051/JPHYSCOL:19955120
Kai-Erik Elers, M. Ritala, M. Leskelä, Leena‐Sisko Johansson
AlN thin films were grown by the Atomic Layer Epitaxy (ALE) technique employing AlCl 3 and NH 3 as precursors. A growth rate of 1.0 A/cycle was obtained in experiments carried out at 500 °C. The films deposited onto soda lime glass substrates were polycrystalline exhibiting a strong preferred orientation in the [001] direction. X-ray Photoelectron Spectroscopy (XPS) measurements revealed that the films contained oxygen and chlorine as impurities.
以alcl3和nh3为前驱体,采用原子层外延(ALE)技术制备了AlN薄膜。在500℃条件下的生长速率为1.0 A/循环。沉积在钠石灰玻璃衬底上的薄膜是多晶的,在[001]方向上表现出强烈的优先取向。x射线光电子能谱(XPS)测量表明,薄膜中含有氧和氯作为杂质。
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引用次数: 10
Investigation of the substrate/epitaxial interface of Si/Si1−xGex layers grown by LPCVD LPCVD生长Si/Si1−xGex层衬底/外延界面的研究
Pub Date : 1995-06-01 DOI: 10.1051/JPHYSCOL:19955106
R. Loo, L. Vescan, C. Dieker, D. Freundt, A. Hartmann, A. Mück
The paper reports a study of the quality of the substrate/epilayer interface. Before growing the Si or Si/Si 1-x Ge x structures by low pressure chemical vapour deposition, Si(100) substrates were cleaned by a modified RCA-cleaning and just before epitaxy different ex-situ and in-situ processes were applied to remove the oxide layer grown on the wafer substrates in the last step of the RCA-cleaning. The effect of interfacial contamination on electrical and optical properties were studied. By a wet-chemical removal of the oxide layer an interfacial oxygen level of 1.3 x 10 13 atoms/cm 2 is found, while a thermal removal leads to an interfacial oxygen level below 6 x 10 12 atoms/cm 2 . In both cases carbon levels of (1-2)x10 14 atoms/cm 2 have been detected. By electrochemical capacitance-voltage profiling it was found that these contaminations are connected with electrically active donors. According to our investigations, electrochemical capacitance-voltage profiling is suitable to give a quick indication on the quality of the substrate/epitaxial interface. In addition, the removal of the oxide layer was investigated by high resolution electron energy loss spectroscopy on cleaned Si-surfaces.
本文报道了衬底/脱膜界面质量的研究。在通过低压化学气相沉积生长Si或Si/Si 1-x Ge x结构之前,用改良的rca清洗方法清洗Si(100)衬底,在外延之前,在rca清洗的最后一步,采用不同的非原位和原位工艺去除生长在晶圆衬底上的氧化层。研究了界面污染对材料电学和光学性能的影响。通过湿法化学去除氧化层,发现界面氧水平为1.3 x 1013原子/ cm2,而热去除导致界面氧水平低于6 x 1012原子/ cm2。在这两种情况下,碳水平均为(1-2)× 10 14原子/平方厘米。通过电化学电容电压谱分析,发现这些污染物与电活性供体有关。根据我们的研究,电化学电容电压谱适合于快速指示衬底/外延界面的质量。此外,用高分辨电子能量损失谱法研究了氧化层的去除。
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引用次数: 0
Thermodynamic Analysis of the Chemical Vapor Deposition of Phosphorus Nitride (P3N5) Thin Films 化学气相沉积氮化磷(P3N5)薄膜的热力学分析
Pub Date : 1995-06-01 DOI: 10.1051/JPHYSCOL:1995506
S. Eroglu
Thermodynamic analysis of the chemical vapor deposition (CVD) of P 3 N 5 has been performed using the method of the minimization of the Gibbs' free energy in order to evaluate the PH 3 -NH 3 -N 2 , PCl 3 -NH 3 -H 2 and PBr 3 -NH 3 -H 2 gaseous mixtures for their potential to synthesize single-phase P 3 N 5 films at high yields. The conditions for the deposition of P 3 N 5 have been determined as a function of input reactant gas ratio of PX 3 /(PX 3 +NH 3 ) (X=H or Cl or Br) and deposition temperature at atmospheric pressure. A single phase P 3 N 5 is deposited at almost all reactant ratios and at temperatures below about 700 K when the PH 3 -NH 3 -N 2 system is used. The use of halide gas mixtures limits the formation of single phase P 3 N 5 to narrow regions of temperature and input reactant gas ratio. The gaseous species generally present in greatest abundance are H 2 , N 2 , NH 3 , PH 3 , HCl, P 4 , PCl 3 , P 2 , HBr, PBr 3 and PN. The thermodynamic analysis suggests that among the systems investigated here, the PH 3 -NH 3 -N 2 mixture is the most promising because simultaneously it gives the highest P 3 N 5 deposition yield and allows better control of the CVD process for the synthesis of P 3 N 5 films.
采用最小吉布斯自由能法对p3n5的化学气相沉积(CVD)进行了热力学分析,以评价ph3 - nh3 - n2、PCl 3 - nh3 - h2和PBr 3 - nh3 - h2气体混合物高产率合成单相p3n5薄膜的潜力。确定了p3n5的沉积条件为p3n5的输入反应物气体比p3n3 /(p3n3 + nh3) (X=H或Cl或Br)和常压下沉积温度的函数。当使用ph3 - nh3 - n2体系时,在几乎所有的反应物比和低于约700 K的温度下都能沉积单相p3n5。卤化物气体混合物的使用限制了形成单相p3n5的温度和输入反应物气体比的狭窄区域。通常丰度最高的气态物质有h2、n2、nh3、ph3、HCl、p4、pcl3、p2、HBr、pbr3和PN。热力学分析表明,在本文研究的体系中,ph3 - nh3 - n2混合物是最有前途的,因为它同时提供了最高的p3n5沉积收率,并且可以更好地控制CVD过程来合成p3n5薄膜。
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引用次数: 0
Physical Properties of Gallium Indium Nitride Films Prepared by Photo-Assisted MOVPE 光辅助MOVPE制备氮化镓铟薄膜的物理性质
Pub Date : 1995-06-01 DOI: 10.1051/JPHYSCOL:19955139
T. Nagatomo, O. Omoto
The optical and electrical properties, crystallinity, and photoluminescence of GaInN epitaxial films were remarkably improved by photo-assited MOVPE using ultraviolet (UV) light from a deuterium (D 2 ) lamp. The dissociation of NH 3 is promoted by irradiation with a D 2 lamp and indiun atoms are effectively incorporated into the crystal lattice of GaInN. Good-quality epitaxial GaInN films were obtained at higher growth temperature of 800°C increasing the now rate of trimethylindium (TMIn). The photoluminescence peak intensity (band-edge emission) of GaInN films grown at 800°C is 14 times as great as that of 675°C.
利用氘(d2)灯的紫外(UV)光辅助MOVPE,可以显著提高GaInN外延膜的光学和电学性能、结晶度和光致发光性能。在d2灯的照射下,nh3的解离被促进,独立原子被有效地结合到GaInN的晶格中。在800℃的生长温度下获得了高质量的外延GaInN薄膜,提高了三甲基lindium (TMIn)的现收率。800℃下生长的GaInN薄膜的光致发光峰值强度(带边发射)是675℃时的14倍。
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引用次数: 0
Mass Spectrometric Study of Copper(II) β-Diketonates Vapour Thermolysis Mechanism and Kinetics 铜(II) β-二酮酸酯蒸气热裂解机理及动力学的质谱研究
Pub Date : 1995-06-01 DOI: 10.1051/JPHYSCOL:1995525
A. E. Turgambaeva, A. Bykov, I. Igumenov
Vapour thermolysis processes of copper(II) bis-chelate complexes with different β-diketones in the 160-640°C temperature range were studied by using the high-temperature source of a molecular beam with mass spectrometric recording of the gas phase composition directly at the outlet from the thermal reactor. Schemes of a heterogeneous decomposition of these compounds vapour were suggested on the basis of temperature dependences of the thermolysis gaseous products composition. It was established that the mechanisms of thermal conversion of copper(II) complexes with fluorinated and non-fluorinated ligands were not similar. A comparison of the thermal behaviour of the complexes with fluorinated and non-fluorinated ligands in vacuum, hydrogen and oxygen was carried out. Effective values of kinetic parameters in the Arrhenius equation were calculated for the first-order reaction on initial compound from the temperature dependence of the rate constant. The sequence of copper(II) complexes with β-diketones having different end substituents according to the thermal stability was revealed from the values of the thermal decomposition activation energy.
采用分子束高温源,研究了不同β-二酮铜(II)双螯合物在160 ~ 640℃温度范围内的蒸汽热裂解过程,并在热反应器出口直接用质谱法记录了气相组成。根据热分解产物组成的温度依赖性,提出了这些化合物蒸汽的非均相分解方案。结果表明,铜(II)配合物与氟化配体和非氟化配体的热转化机理不相似。比较了含氟和非氟配体配合物在真空、氢和氧条件下的热行为。根据反应速率常数的温度依赖性,计算了初始化合物一级反应的动力学参数有效值。根据热分解活化能的值,揭示了铜(II)配合物与端取代基不同的β-二酮配合物的热稳定性顺序。
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引用次数: 7
Modelling binary, Knudsen and transition regime diffusion inside complex porous media 复杂多孔介质内二元扩散、Knudsen扩散和过渡扩散模型
Pub Date : 1995-06-01 DOI: 10.1051/JPHYSCOL:1995517
G. Vignoles
The problem of gaseous diffusion inside complex porous media arises in the modeling of many chemical processes (e.g. Chemical Vapor Infiltration (CVI), heterogeneous catalysis in porous catalysts, filtration, etc...). A program computing effective diffusivities in the bulk, Knudsen and transition regimes has been designed and tested, which uses a Monte-Carlo mean-square-displacement algorithm. The porous medium has been represented from a special interpretation of a computer 3D discretized image. Simulations were carried out in a typical case of complex structured porous medium: a stacking of tissues (e. g. 2D woven fiber preform for CVI-densified composite materials). The results are presented as tortuosity factors, i.e. deviations from an equivalent medium made of straight cylindrical pores. The evolution of the diffusivities with the geometrical parameters of the tissues, and with the stacking mode has also been studied. It appears that the perpendicular diffusivity is closely related to the proportion of matching holes between different layers of tissue. The intermediate regime appears for Knudsen numbers lying between 100 and 10 -1 . In this domain, the Bosanquet formula only gives a good description if the Knudsen number is multiplied by a factor γ = 1/4. This phenomenon had been reported, to a lesser extent, for unidirectional random fiber packings.
复杂多孔介质中的气体扩散问题出现在许多化学过程的建模中(例如化学蒸汽渗透(CVI)、多孔催化剂中的非均相催化、过滤等)。一个程序计算有效扩散在大块,Knudsen和过渡制度已经设计和测试,它使用蒙特卡罗均方位移算法。通过对计算机三维离散图像的特殊解释来表示多孔介质。在复杂结构多孔介质的典型情况下进行了模拟:组织堆积(例如用于cvi致密复合材料的二维编织纤维预制体)。结果表现为扭曲因子,即与由直圆柱孔组成的等效介质的偏差。研究了扩散系数随组织几何参数和堆积方式的变化规律。结果表明,垂直扩散系数与不同组织层间匹配孔的比例密切相关。中间状态出现在克努森数介于100和10 -1之间。在这个域中,只有当Knudsen数乘以一个因子γ = 1/4时,Bosanquet公式才能给出一个很好的描述。这种现象在较小程度上也见于单向随机纤维填料。
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引用次数: 42
Plasma-Assisted Deposition at Atmospheric Pressure 大气压下等离子体辅助沉积
Pub Date : 1995-06-01 DOI: 10.1051/JPHYSCOL:1995569
J. Salge
In plasma-assisted deposition methods the activation energy necessary for the initiation of chemical reactions is transferred via charged particles. Due to this fact in many cases the process temperature can be kept small, if gas discharges at pressures below 1 hPa are used. On the other hand low pressure requires a great deal of vacuum equipment. Processes at atmospheric pressure are more favourable, if similar results compared to existing methods can be achieved. Basis for a new plasma-assisted deposition method at atmospheric pressure are barrier discharges. Those discharges consist of a large number of transient microdischarges in parallel which are distributed statistically on the surface to be coated. Starting with some basic considerations on the repetitive generation of microdischarges, the deposition of thin polymeric films on glass surfaces is described, using barrier discharges at atmospheric pressure and acetylene. Uniform polymeric films up to 1 μm are obtained, if trains of voltage pulses are used. Parameters influencing the deposition rate and the film quality are discussed. In addition, it is estimated whether further improvements of the deposition process are possible.
在等离子体辅助沉积方法中,引发化学反应所需的活化能通过带电粒子传递。由于这一事实,在许多情况下,如果气体排放压力低于1hpa,则可以保持较小的工艺温度。另一方面,低压需要大量的真空设备。如果能获得与现有方法相似的结果,在常压下的过程是更有利的。一种新的常压等离子体辅助沉积方法的基础是阻挡放电。这些放电由大量并联的瞬态微放电组成,这些微放电统计分布在待涂覆表面上。从重复产生微放电的一些基本考虑开始,描述了在常压和乙炔下使用阻挡放电在玻璃表面沉积聚合物薄膜。如果使用电压脉冲串,可以得到厚度达1 μm的均匀聚合物薄膜。讨论了影响沉积速率和薄膜质量的参数。此外,估计是否有可能进一步改进沉积工艺。
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引用次数: 73
期刊
Le Journal De Physique Colloques
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