Al-Raeei Marwan
Faculty of Sciences, Damascus University, Damascus, Syria.
J Phys Condens Matter. 2022 May 11;34(28). doi: 10.1088/1361-648X/ac6a9b.
Morse potential interaction is an important type of the vibrational potentials, especially, in the quantum mechanics which is used for the describing of general vibrational cases rather than the harmonic one. Morse potential has three fitting parameters, the depth of the Morse interaction, the distance of equilibrium bond and the range parameter which determines the range of the well. The Morse interaction specific bond volume is a three dimensional image of the bond length in its molar case, and this specific volume is the generalisation in three dimensions. In this study, the integral equation theory of the simple fluids has been applied for deriving a novel formula of the specific bond volume for Morse potential based on one of the approaches in the theory and based on the boundary conditions. We find that the specific bond volume of Morse potential depends on the absolute temperature via logarithmic function and square root function, besides, the specific bond volume of Morse potential decreases when the temperature decreases for different values of the molar volume and for different values of the depth of Morse well. In addition to that, the specific bond volume of Morse potential increases when the depth of the well decreases for different temperature values. Also, it is found from the formula which we derive that the specific bond volume of Morse potential increases via linear function with the molar volume of the system for different values of temperatures. We apply the formula of the specific bond volume of Morse potential for finding this specific volume for two molecules of the hydrogen halogens, which are the hydrogen chloride, and hydrogen fluoride. We find that the specific bond volume of the hydrogen chloride is greater than the one of the hydrogen fluoride. Also, we apply the formula for the two simple molecules gases which are the hydrogen molecules, and the nitrogen molecules. Besides, we apply the formula for the slab-slider system in two cases: hard and soft materials, and we concluded that the changes of the specific bond volume of the soft materials is faster than the hard materials. We believe that the formula which is found of the specific bond volume of Morse potential is general and can be applied for multiple materials.
莫尔斯势相互作用是振动势的一种重要类型,特别是在用于描述一般振动情况而非简谐振动情况的量子力学中。莫尔斯势有三个拟合参数,即莫尔斯相互作用深度、平衡键距以及决定势阱范围的范围参数。莫尔斯相互作用比体积是其摩尔情况下键长的三维图像,且这种比体积是三维的推广。在本研究中,基于简单流体的积分方程理论中的一种方法并依据边界条件,推导出了一个关于莫尔斯势比体积的新公式。我们发现,莫尔斯势的比体积通过对数函数和平方根函数依赖于绝对温度,此外,对于不同的摩尔体积值和不同的莫尔斯势阱深度值,当温度降低时,莫尔斯势的比体积会减小。除此之外,对于不同的温度值,当势阱深度减小时,莫尔斯势的比体积会增大。同样,从我们推导的公式中发现,对于不同的温度值,莫尔斯势的比体积随系统的摩尔体积呈线性函数增加。我们应用莫尔斯势比体积公式来计算两种卤化氢分子(即氯化氢和氟化氢)的这种比体积。我们发现氯化氢的比体积大于氟化氢的比体积。此外,我们将该公式应用于两种简单分子气体,即氢分子和氮分子。另外,我们将该公式应用于平板 - 滑块系统的两种情况:硬材料和软材料,并得出软材料比体积的变化比硬材料快的结论。我们认为所发现的莫尔斯势比体积公式具有通用性,可应用于多种材料。