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arXiv:1408.4003 · Journal of Mathematical Physics

Quantum mechanics without potential function

A. D. Alhaidari, M. E. H. Ismail

Published Jul 1, 2015• 41 citations
arXivHTMLPDF

Abstract

In the standard formulation of quantum mechanics, one starts by proposing a potential function that models the physical system. The potential is then inserted into the Schrödinger equation, which is solved for the wavefunction, bound states energy spectrum, and/or scattering phase shift. In this work, however, we propose an alternative formulation in which the potential function does not appear. The aim is to obtain a set of analytically realizable systems, which is larger than in the standard formulation and may or may not be associated with any given or previously known potential functions. We start with the wavefunction, which is written as a bounded infinite sum of elements of a complete basis with polynomial coefficients that are orthogonal on an appropriate domain in the energy space. Using the asymptotic properties of these polynomials, we obtain the scattering phase shift, bound states, and resonances. This formulation enables one to handle not only the well-known quantum systems but also previously untreated ones. Illustrative examples are given for two- and three-parameter systems.

DOI
10.1063/1.4927262

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In the standard formulation of quantum mechanics, one starts by proposing a potential function that models the physical system. The potential is then inserted into the Schrödinger equation, which is solved for the wavefunction, bound states energy spectrum, and/or scattering phase shift. In this work, however, we propose an alternative formulation in which the potential function does not appear. The aim is to obtain a set of analytically realizable systems, which is larger than in the standard formulation and may or may not be associated with any given or previously known potential functions. We start with the wavefunction, which is written as a bounded infinite sum of elements of a complete basis with polynomial coefficients that are orthogonal on an appropriate domain in the energy space. Using the asymptotic properties of these polynomials, we obtain the scattering phase shift, bound states, and resonances. This formulation enables one to handle not only the well-known quantum systems but also previously untreated ones. Illustrative examples are given for two- and three-parameter systems.
We propose a formulation of quantum mechanics for a finite level system whose potential function is not realizable and/or analytic solution of the wave equation is not feasible. The system's wavefunction is written as an infinite sum in a complete set of square integrable functions. Interaction in the theory is introduced in function space by a real finite tridiagonal symmetric matrix. The expansion coefficients of the wavefunction satisfy a three-term recursion relation incorporating the parameters of the interaction. Information about the structure and dynamics of the system is contained in the scattering matrix, which is defined in the usual way. The bound state energy spectrum (system's structure) is finite. Apart from the 2M − 1 dimensionless parameters of the interaction matrix, whose rank is M, the theory has one additional scale parameter. In the development, we utilize the kinematic tools of the J-matrix method.
We present a formulation of quantum mechanics based on orthogonal polynomials. The wavefunction is expanded over a complete set of square integrable basis in configuration space where the expansion coefficients are orthogonal polynomials in the energy. Information about the corresponding physical systems (both structural and dynamical) are derived from the properties of these polynomials. We demonstrate that an advantage of this formulation is that the class of exactly solvable non-relativistic quantum mechanical problems becomes larger than in the conventional formulation (see, for example, Table 1 in the text).
Following the celebrated postulates of quantum mechanics, we write the quantum mechanical wavefunction as a convergent series of suitably selected complete square-integrable basis functions in configuration space. The expansion coefficients of the series are energy orthogonal polynomials that contain all spectral information about the system. We exploit the properties of these polynomials to introduce physical systems with rich and highly nontrivial energy spectra. In this approach, no reference is made at all to the usual potential energy function. We consider, in this new approach, a few representative problems at the level of undergraduate students who took at least two courses in quantum mechanics and are familiar with the basics of orthogonal polynomials. Our aim is to expose students to quantum systems with rich energy spectra that goes beyond the very limited textbook examples of systems with very simple energy spectra (e.g., the harmonic oscillator, Coulomb, Morse, Pöschl–Teller, etc.) illustrating the physical significance of these energy polynomials in the description of a quantum system. To assist students, partial solutions are given in an appendix as tables and figures.
Abstract We present a formulation of quantum mechanics based on the theory of orthogonal polynomials. The wavefunction is expanded over a complete set of square integrable basis where the expansion coefficients are orthogonal polynomials in the energy and physical parameters. Information about the corresponding physical systems (both structural and dynamical) are derived from the properties of these polynomials. We demonstrate that an advantage of this formulation is that the class of exactly solvable quantum mechanical problems becomes larger than in the conventional formulation (see, for example, table 3 in the text). We limit our investigation in this work to the Askey classification scheme of hypergeometric orthogonal polynomials and focus on the Wilson polynomial and two of its limiting cases (the Meixner–Pollaczek and continuous dual Hahn polynomials). Nonetheless, the formulation is amenable to other classes of orthogonal polynomials.