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The chemical vapor deposition of polycrystalline silicon nitride films at low temperatures.

机译:在低温下化学气相沉积多晶硅氮化硅膜。

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Polycrystalline films of {dollar}rm Sisb3Nsb4{dollar} (silicon nitride) were deposited by CVD (chemical vapor deposition) at relatively low temperatures, as low as 1150{dollar}spcirc{dollar}C, and high growth rates, e.g, 450 {dollar}mu{dollar}m/hr at 1190{dollar}spcirc{dollar}C. Previously, crystalline growth at these rates has been reported only at temperatures above 1350{dollar}spcirc{dollar}C. The high growth rates, which were attained at technologically reasonable temperatures, makes CVD {dollar}rm Sisb3Nsb4{dollar} a more promising candidate for protective coatings for high temperature applications. Crystalline film growth was attained at low temperatures by manipulating the crystalline nucleation process. Mechanisms leading to low temperature crystalline nucleation were studied.; Crystalline film deposition occurred over a very narrow range of CVD process parameters, {dollar}rm SiHsb4{dollar} or NH{dollar}sb3{dollar} inlet concentrations or temperature. At these lower temperatures, crystalline film growth was nucleation limited. Invariably, nucleation occurred on a growing amorphous interlayer the composition of which gradually changed from Si-rich near the substrate to stoichiometric amorphous silicon nitride at its surface where the crystalline film nucleated abruptly. Detailed characterization of the nucleation process was performed with a combination of FT-IR, XPS, X-ray diffraction and TEM. Film nucleation on a growing interlayer complicates both classical and atomistic treatments of nucleation theory. It was proposed that the chemical and localized atomic structure of the interlayer controls the nucleation event.; In order to more easily control poly-crystalline film growth, a two step CVD process was developed which enabled low temperature, crystalline film growth on a variety of substrates, metal and ceramic. Additionally, the effect of CVD process conditions on film surface morphology and chemical composition were analyzed, and explanations, some of which were different than traditional CVD arguments, were proposed.; CVD was performed in an impinging jet configuration, a configuration in which mass transport is well defined and which allowed simple kinetic modeling of the growth process. Crystalline growth was first order dependent on SiH{dollar}sb4{dollar} concentration and not dependent on NH{dollar}sb3{dollar} concentrations greater than 0.2. An activation energy of 9600/R was measured which is remarkably similar to poly-crystalline Si growth. This could imply that SiH{dollar}sb{lcub}rm x{rcub}{dollar} species are rate limiting.; By coating the films with a silicon oxynitride layer, enhanced oxidation resistance was achieved. High diamond nucleation densities were obtained in a preliminary study.
机译:通过CVD(化学气相沉积)在相对低的温度(低至1150 {)和高生长速率(例如450)下通过化学气相沉积(CVD)沉积{rm} Sisb3Nsb4 {美元}的多晶膜(氮化硅)。 1190 {dol} mu {dollar} m / hr {sp} {dollar} C。以前,仅在高于1350℃的温度下才报道了以这些速率生长的晶体。在技​​术上合理的温度下获得的高生长速率使CVD {Sirm} Sisb3Nsb4 {USD}成为用于高温应用的保护涂层的更有希望的候选者。通过控制晶体成核过程,可以在低温下获得结晶膜的生长。研究了导致低温晶体成核的机理。结晶膜的沉积发生在非常窄的CVD工艺参数范围内,例如入口SiHsb4或NHsb3进口浓度或温度。在这些较低的温度下,结晶膜的生长受到成核作用的限制。不断地,成核发生在生长的非晶态中间层上,该非晶态中间层的组成从衬底附近的富硅逐渐变为表面成膜的化学计量的非晶态氮化硅。结合FT-IR,XPS,X射线衍射和TEM对成核过程进行了详细的表征。在不断增长的中间层上成膜的成核使成核理论的经典处理和原子处理都变得复杂。提出了中间层的化学和局部原子结构控制成核事件。为了更容易地控制多晶膜的生长,开发了一种两步CVD工艺,该工艺能够在各种基材(金属和陶瓷)上低温结晶膜的生长。此外,分析了CVD工艺条件对薄膜表面形貌和化学成分的影响,并提出了一些解释,其中一些解释与传统的CVD观点不同。 CVD是在撞击射流构型中进行的,该构型中定义了良好的质量传递,并允许对生长过程进行简单的动力学建模。晶体生长是一阶依赖于SiH {sb4 {dollar}的浓度,而不是依赖于NH {dollar} sb3 {dollar}的浓度大于0.2。测得的活化能为9600 / R,与多晶硅的生长非常相似。这可能意味着SiH {dollar} sb {lcub} rm x {rcub} {dollar}物种是限速的。通过用氮氧化硅层涂覆膜,获得增强的抗氧化性。在初步研究中获得了较高的金刚石成核密度。

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