ROTATIONAL-VIBRATIONAL EIGEN SOLUTIONS OF THE D-DIMENSIONAL SCHRÖDINGER EQUATION FOR THE IMPROVED WEI POTENTIAL

In this present study, we have employed the techniques of exact quantization rule and ansatz solution method to obtain closed form expressions for the rotational-vibrational eigensolutions of the D-dimensional Schrödinger equation for the improved Wei potential, for cases of h′ ≠ 0 and h′ = 0. By using our derived energy equation and choosing arbitrary values of n and ℓ, we have computed the bound state rotational-vibrational energies of CO, H2 and LiH for various quantum states. The mean absolute percentage deviation (MAPD) and the Lippincott criterion ware used as a goodness-of-fit indices to compare our result with the Rydberg-Klein-Rees (RKR) and improved Tietz potential data in the literature. MAPD of 0.2862%, 0.2896% and 0.0662% relative to the RKR data for CO ware obtained. For the improved Wei and Morse potential, our computed energy eigenvalues for CO, H2 and LiH are in excellent agreement with existing results in the literature

Approximate analytical solutions for arbitrary l-state of the Hulthén potential with an improved approximation of the centrifugal term

An approximate analytical solution of the radial Schrödinger equation for the generalized Hulthén potential is obtained by applying an improved approximation of the centrifugal term. The bound state energy eigenvalues and the normalized eigenfunctions are given in terms of hypergeometric polynomials. The results for arbitrary quantum numbers n r and l with different values of the screening parameter δ are compared with those obtained by the numerical method, asymptotic iteration, the Nikiforov-Uvarov method, the exact quantization rule, and variational methods. The results obtained by the method proposed in this work are in a good agreement with those obtained by other approximate methods.

Application of the exact quantization rule for some noncentral separable potentials

The energy spectrum of some noncentral separable potentials are obtained using the exact quantization rule in r and θ dimensions. The results are consistent with those obtained by other methods. PACS Nos.: 03.65.Ca, 03.65.Ge

Arbitrary /-state approximate solutions of the Hulthén potential through the exact quantization rule

In this paper, using the Exact Quantization Rule, we present approximate analytical solutions of the radial Schrödinger equation with non-zero l values for the Hulthén potential in the frame of an approximation to the centrifugal potential for any l states. The energy levels of all bound states can be easily calculated from the Exact Quantization Rule. Specifically, the normalized analytical wave functions are also obtained. Some energy eigenvalues are numerically calculated and compared with those obtained by other methods such as asymptotic iteration, supersymmetry, numerical integration methods, and the schroedinger Mathematica package.

EXACT QUANTIZATION RULE AND ITS APPLICATIONS TO PHYSICAL POTENTIALS

By using the exact quantization rule, we present analytical solutions of the Schrödinger equation for the deformed harmonic oscillator in one dimension, the Kratzer potential and pseudoharmonic oscillator in three dimensions. The energy levels of all the bound states are easily calculated from this quantization rule. The normalized wavefunctions are also obtained. It is found that the present approach can simplify the calculations.