The rotating Morse potential model for diatomic molecules in the J-matrix representation: II. The S-matrix approach
arXiv:0810.1322 · doi:10.1088/0953-4075/41/21/215001
Abstract
This is the second article in which we study the rotating Morse potential model for diatomic molecules using the tridiagonal J-matrix approach. Here, we improve further the accuracy of computing the bound states and resonance energies for this potential model from the poles of the S-matrix for arbitrary angular momentum. The calculation is performed using an infinite square integrable basis that supports a tridiagonal matrix representation for the reference Hamiltonian, which is included in the computations analytically without truncation. Our method has been applied to both the regular and inverted Morse potential with favorable results in comparison with available numerical data. We have also shown that the present method adds few significant digits to the accuracy obtained from the finite dimensional approach (e.g. the complex rotation method). Moreover, it allows us to handle easily both analytic and non-analytic potentials as well as 1/r singular potentials.
11 pages, 4 tables, and 1 color figure
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Cited by in corpus (5)
- Resonant states and pseudospin symmetry in the Dirac Morse potential
- Singular Short Range Potentials in the J-Matrix Approach
- Analytical Treatment of the Oscillating Yukawa Potential
- Energy spectrum of a generalized Scarf potential using the Asymptotic Iteration Method and the Tridiagonal Representation Approach
- J-matrix method of scattering for potentials with inverse square singularity: The real representation