CVD-COMPOSITES AND SALINE SOLUTIONS-MELTS: SIMILARITY AND DIFFERENCES

V. Zinchenko, V. V. Menchuk
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Abstract

The general features and specific peculiarities of the thermodynamics of the processes occurring during the evaporation of CVD (Chemical Vapor Deposition) – composites based on germanium – metal chalcogenide systems and dissolution of poorly soluble compounds in salt melts are considered. The essence of both processes consists in the occurrence of exchange reactions between the initial components with the formation of highly volatile substances in the first case and highly soluble compounds in the second. Both processes are endothermic in their thermochemical essence, and their course is facilitated by the entropy component, the role of which increases with increasing temperature, deepening of the vacuum in the case of CVD composites, and dilution of the saline solution – melt. The peculiarities due to the difference between vacuum and salt melt in nature have also been established. If the interaction of molecules in a rarefied molecular vapor of evaporation products can be practically neglected, then in a salt solution-melt, as in a highly concentrated system, secondary reactions of complexation of ions and molecules of the dissolved compound and the main ions of the melt are characteristic. The latter factor significantly affects the solubility in the salt melt due to the shift in equilibrium. Kinetic factors, which differ significantly in both processes, are essential in the reverse reactions of condensation of a CVD‑composite vapor on a substrate and in the deposition of crystals during the crystallization of a solute from a salt melt. Due to the much higher rate of vapor condensation on the substrate, more significant vapor saturation is achieved and, accordingly, the nucleation rate than during crystallization of the salt melt. Therefore, the probability of nanostructuring or complete amorphization of a coating obtained from a CVD‑composite is much higher than for a salt solution-melt, in which the ability to form nanostructures is more limited.
cvd -复合材料与盐溶液-熔体:异同
讨论了锗-金属硫族化物体系CVD(化学气相沉积)-复合材料蒸发过程和难溶性化合物在盐熔体中溶解过程热力学的一般特征和特殊特点。这两个过程的本质在于初始组分之间发生交换反应,在第一种情况下形成高挥发性物质,在第二种情况下形成高可溶性化合物。从热化学本质上讲,这两个过程都是吸热过程,熵分量促进了这一过程,熵分量的作用随着温度的升高、CVD复合材料真空度的加深和盐溶液熔体的稀释而增加。由于真空和盐熔体在自然界中的不同而产生的特性也得到了证实。如果在稀薄的蒸发产物的分子蒸气中分子的相互作用实际上可以忽略不计,那么在盐溶液-熔体中,就像在高度浓缩的系统中一样,溶解化合物的离子和分子以及熔体的主要离子的络合的二次反应是有特点的。后一个因素由于平衡的转移而显著影响盐熔体中的溶解度。动力学因素在两种过程中都有很大的不同,但在CVD复合气相在衬底上凝结的反反应和盐熔体中溶质结晶过程中晶体沉积的过程中,动力学因素是必不可少的。由于基材上的蒸汽冷凝速率高得多,因此实现了更显著的蒸汽饱和,相应地,比盐熔体结晶期间的成核速率高。因此,CVD -复合材料涂层形成纳米结构或完全非晶化的可能性比盐溶液-熔体涂层高得多,而盐溶液-熔体形成纳米结构的能力更有限。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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