Generalized Rayleigh-Schrödinger perturbation theory

1972 ◽  
Vol 6 (4) ◽  
pp. 609-611 ◽  
Author(s):  
Ramón Carbó
Keyword(s):  
Perturbation Theory ◽  
Schrödinger Perturbation

Applicability of the schrödinger perturbation theory to bound states

1964 ◽  
Vol 10 (1) ◽  
pp. 73 ◽  
Author(s):  
K. Hausmann ◽  
W. Macke ◽  
P. Ziesche
Keyword(s):  
Perturbation Theory ◽  
Bound States ◽  
Schrödinger Perturbation

scholarly journals Quantum square-well with logarithmic central spike

2018 ◽  
Vol 33 (02) ◽  
pp. 1850009 ◽  
Author(s):  
Miloslav Znojil ◽  
Iveta Semorádová
Keyword(s):  
Perturbation Theory ◽  
Boundary Conditions ◽  
Closed Form ◽  
Wave Functions ◽  
Change Of Variables ◽  
State Dependent ◽  
Square Well ◽  
Strength Formula ◽  
Schrödinger Perturbation ◽  
Dependent Interaction

Singular repulsive barrier [Formula: see text] inside a square-well is interpreted and studied as a linear analog of the state-dependent interaction [Formula: see text] in nonlinear Schrödinger equation. In the linearized case, Rayleigh–Schrödinger perturbation theory is shown to provide a closed-form spectrum at sufficiently small [Formula: see text] or after an amendment of the unperturbed Hamiltonian. At any spike strength [Formula: see text], the model remains solvable numerically, by the matching of wave functions. Analytically, the singularity is shown regularized via the change of variables [Formula: see text] which interchanges the roles of the asymptotic and central boundary conditions.

APPROXIMATE MOLECULAR ORBITALS: III. THE 1sσ AND 2pπ STATES OF HeH++

1967 ◽  
Vol 45 (7) ◽  
pp. 2231-2238 ◽  
Author(s):  
M. Cohen ◽  
R. P. McEachran ◽  
Sheila D. McPhee
Keyword(s):  
Perturbation Theory ◽  
Molecular Orbitals ◽  
Wave Functions ◽  
Variational Techniques ◽  
Approximate Wave ◽  
Schrödinger Perturbation

A combination of Rayleigh–Schrödinger perturbation theory and variational techniques, previously used to calculate the wave functions of the lowest σ and π states of H2+ has been applied to the 1sσ and 2pπ states of HeH++. The accuracy of the resulting approximate wave functions is demonstrated by comparing a number of quantities calculated with them with the corresponding exact values.

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