Solutions of Schrodinger equation and thermodynamic properties of Iodine and Scandium Fluoride molecules based on Formula method

The study presents the thermodynamic properties of the Iodine and Scandium Flouride molecules with molecular Deng-Fan potential. The bound state energy solution of the radial Schrodinger equation is obtained via the formula method. The partition function and other thermodynamic properties are evaluated via the Poisson summation approach. The numerical values of energy of the I2 and ScF molecules are found to be in agreement with results obtained from other methods in the literature. The results further show that the partition function decreases, and then converges to a constant value as temperature increases.

Fourth derivative singularly P-stable method for the numerical solution of the Schrödinger equation

In this paper, we construct a method with eight steps that belongs to the family of Obrechkoff methods. Due to the explicit nature of the new method, not only does it not require another method as predictor, but it can also be considered as a suitable predictive technique to be used with implicit methods. Periodicity and error terms are studied when applied to solve the radial Schrödinger equation, considering different energy levels. We show its advantages in terms of accuracy, consistency, and convergence in comparison with other methods of the same order appearing in the literature.

Solutions of Schrodinger Equation And Thermodynamic Properties of Potassium Dimer Based On Formular Method

The study presents the thermodynamic properties of the XI Σ+g state of potassium (K2) dimer with molecular Deng-Fan potential. The bound state energy solution of the radial Schrodinger equation is obtained via the formula method. The partition function and other thermodynamic properties are evaluated. The numerical values of energy are found to be in agreement with results obtained from other methods in literature. The results further show that the partition function increases as temperature decreases, which implies a decrease in the probability of finding a particle in a state with quantum number, n.

Masses and Thermodynamic Properties of a Quarkonium System

Hulthen plus Hellmann potentials are adopted as the quark-antiquark interaction potential for studying the thermodynamic properties and the mass spectra of heavy mesons. We solved the radial Schrödinger equation analytically using the Nikiforov-Uvarov method. The energy eigenvalues and corresponding wave function in terms of Laguerre polynomials were obtained. The present results are applied for calculating the mass of heavy mesons such as charmoniumand cc and bottomonium bb, and thermodynamic properties such as the mean energy, the specific heat, the free energy, and the entropy. Four special cases were considered when some of the potential parameters were set to zero, resulting in Hellmann potential, Yukawa potential, Coulomb potential, and Hulthen potential, respectively. The present potential provides satisfying results in comparison with experimental data and the work of other researchers.

Exact Solution of the Schrödinger Equation for Composition of Coulomb and Oscillator Potentials

The spherically symmetric potential is considered whose dependence on the distance r is described by the smooth composition of Coulomb at r < r0 and oscillator at r > r0 potentials. The boundary distance r0 is determined by the parameters of these potentials. The exact continuous solution of the radial Schrödinger equation is expressed in terms of the confluent hypergeometric functions. The discrete energy levels are obtained. The graphic illustrations for the energy spectrum and the radial wave functions are presented.

Degenerate Canonical Forms of Ordinary Second-Order Linear Homogeneous Differential Equations

For each fundamental and widely used ordinary second-order linear homogeneous differential equation of mathematical physics, we derive a family of associated differential equations that share the same “degenerate” canonical form. These equations can be solved easily if the original equation is known to possess analytic solutions, otherwise their properties and the properties of their solutions are de facto known as they are comparable to those already deduced for the fundamental equation. We analyze several particular cases of new families related to some of the famous differential equations applied to physical problems, and the degenerate eigenstates of the radial Schrödinger equation for the hydrogen atom in N dimensions.

Approximate solutions of the Schrödinger equation with Hulthén-Hellmann Potentials for a Quarkonium system

Hulthén plus Hellmann potentials are adopted as the quark-antiquark interaction potential for studying the mass spectra of heavy mesons. We solved the radial Schrödinger equation analytically using the Nikiforov-Uvarov method. The energy eigenvalues and corresponding wave function in terms of Laguerre polynomials were obtained. The present results are applied for calculating the mass of heavy mesons such as charmonium and bottomonium. Four special cases were considered when some of the potential parameters were set to zero, resulting into Hellmann potential, Yukawa potential, Coulomb potential, and Hulthén potential, respectively. The present potential provides satisfying results in comparison with experimental data and the work of other researchers.

Approximate energy spectra and statistical mechanical functions of some diatomic molecular hydrides

In this study, we have investigated the statistical mechanical properties of the Varshni potential model for some diatomic molecular hydrides via the Euler–Maclaurin formula. This was done using the approximate analytical energy eigenvalues, which were obtained by solving the radial Schrödinger equation with the Greene–Aldrich approximation and suitable coordinate transformation schemes. The effect of high temperatures and upper bound vibration quantum number on the vibrational partition function and other thermodynamic functions of the selected diatomic molecular hydrides were studied. We also show that these effects on the thermodynamic functions considered were similar for all the diatomic molecular hydrides selected.