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arXiv:1504.00030 · Revista Mexicana de Física

Solution of the Schrödinger equation making use of time-dependent constants of motion

G. F. Torres del Castillo

Published Jan 1, 2015• 1 citation
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Abstract

It is shown that if a complete set of mutually commuting operators is formed by constants of motion, then, up to a factor that only depends on the time, each common eigenfunction of such operators is a solution of the Schrödinger equation. In particular, the operators representing the initial values of the Cartesian coordinates of a particle are constants of motion that commute with each other and from their common eigenfunction one readily obtains the Green function.

DOI
10.31349/revmexfis.61.5.376

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•Jan 1, 2014•0 citations
It is shown that if a complete set of mutually commuting operators is formed by constants of motion, then, up to a factor that only depends on the time, each common eigenfunction of such operators is a solution of the Schrödinger equation. In particular, the operators representing the initial values of the Cartesian coordinates of a particle are constants of motion that commute with each other and from their common eigenfunction one readily obtains the Green function.
The postulates of quantum mechanics associate the time-evolution of a system with its time-dependent Schrödinger equation. We start by examining different solutions to this equation for a particle, represented in terms of a Gaussian wave packet, in different scenarios: free, scattered from a potential energy barrier, or trapped in a potential energy well. In some cases, we encounter stationary solutions, in which the probability density does not change in time (a standing wave). These solutions are identified as eigenfunctions of a system Hamiltonian. The properties of the Hamiltonian as a Hermitian operator are introduced, and particularly, the fact that its proper eigenfunctions can compose an orthonormal set, and that the corresponding eigenvalues are real-valued. Learning that all operators that relate to measurables are Hermitian, and that their eigenvalues relate to the measured values, we conclude that the eigenvalues of the energy operator (Hamiltonian) are the energy levels of the quantum system.
Stationary states General properties We shall consider first some general characteristics of the ‘stationary states’. These are eigenfunctions of the Hamiltonian operator: The requirement that ψ satisfies the Schrödinger equation fixes its time dependence: Notice that (4.1.2) can only be a solution if the external potential V is independent of the time: V = V ( x ). The initial function ψ 0 is not arbitrary but must satisfy the time-independent Schrödinger equation (4.1.1). Writing ψ = R e iS /ħ one thus has The following deductions may be made from (4.1.3): ( a ) The probability density is independent of the time: |ψ| 2 = R 2 0 ( X ). ( b ) The quantum potential Q = (- ħ2/2 mR 0 )∇ 2 R 0 is time-independent. Therefore so is the total effective potential: ( c ) The velocity field v = (l/ m )∇ S 0 is independent of time and hence the trajectories, found by solving m = v ( x )| x = x ( t ) , are solutions of Moreover, ψ 0 ( x ) is often a real function for many bound state problems of interest (although not for scattering states) which implies that the velocity is zero. The particle is at rest where one would classically expect it to move since the quantum force (- ∇ Q ) cancels the classical force (- ∇ K ). ( d ) The energy of all particles in the ensemble, -∂ S /∂ t , is a constant of the motion and equal to the energy eigenvalue: with (4.1.4), we have an example of the conservation of energy (cf. §3.9.3). ( e ) The total field energy is conserved: 〈Ĥ〉 = E . […]
In the past few chapters, the Schrödinger equation has been developed and applied to the solution of a number of quantum mechanical problems, mainly to develop experience with the results of simple and common systems. The results from these examples can be summarized relatively simply. In general, quantization enters the problem through the non-commuting nature of conjugate operators such as position and momentum as well as from classical boundary quantization. This has led to the Schrödinger equation itself being the primary equation of motion for the wave function solution to the problem. In essence, duality is incredibly important and is the basic method by which the electron is treated as a wave, rather than as a particle, and the wave equation of interest is the Schrödinger equation. When boundary conditions are applied, either through potential barriers or through the form of the potential (as in the harmonic oscillator), the time-independent Schrödinger equation yields solutions that are often special functions. Examples of this are the sines and cosines in the rectangular-barrier case, the Airy functions in the triangular-well case, and the Hermite polynomials in the harmonic oscillator case.
The time-dependent Schrödinger equation (TDSE) contains two variables: position and time. Therefore, the solutions are functions of both space and time (x and t, if we limit ourselves to particles moving in one dimension). It turns out that the easiest way to "solve" such an equation of two variables is to perform a separation of variables. We show that if the potential does not change with time, then certain special solutions (eigenfunctions) can be written as a product of a space function and a time function: Ψ(x,t) = ψ(x) f(t). By assuming a "separable" solution of this form, and plugging into the TDSE, the TDSE itself can be separated into two equations: the time-independent Schrödinger equation (TISE) with solution ψ(x), and the space-independent Schrödinger equation (SISE) with solution f(t). Furthermore, f(t) always equals e -iωt , while ψ(x) depends on the potential. So, for potentials that do not vary with time, we need only solve the much simpler TISE in order to investigate the energy, momentum, and so on of the particle. This is why, for the remainder of this book, we only use the TISE.
An important feature of the wave equation is that its solutions q(r, t) are uniquely specified once the initial values q(r, 0) and (del)q(r, 0)/@t are specified. As was mentioned before, if we view the wave equation as describing a continuum limit of a network of coupled oscillators, then this result is very reasonable since one must specify the initial position and velocity of an oscillator to uniquely determine its motion. It is possible to write down other “equations of motion” that exhibit wave phenomena but which only require the initial values of the dynamical variable — not its time derivative — to specify a solution. This is physically appropriate in a number of situations, the most significant of which is in quantum mechanics where the wave equation is called the Schrodinger equation. This equation describes the time development of the observable attributes of a particle via the wave function (or probability amplitude) . In quantum mechanics, the complete specification of the initial conditions of the particle’s motion is embodied in the initial value of . The price paid for this change in the allowed initial data while asking for a linear wave equation is the introduction of complex numbers into the equation for the wave. Indeed, the values taken by are complex numbers. In what follows we shall explore some of the elementary features of the wave phenomena associated with the Schrodinger equation.