Abstract
It is shown that calculation of the momentum Fisher information of the quasi-one-dimensional hydrogen atom recently presented by Saha et al (2017 Eur. J. Phys. 38 025103) is wrong. A correct derivation is provided and its didactical advantages and scientific significances are highlighted.
Export citation and abstract BibTeX RIS
Recently, a calculation of the position Iρ and momentum Iγ Fisher information was presented for (i) a linear harmonic oscillator, (ii) a quasi-one-dimensional hydrogen atom and (iii) an infinite potential well [1]. By general definition [2, 3], these quantum-information measures for arbitrary one-dimensional (1D) structures are defined as
where a position integration is carried out over all available interval x and positive integer index n counts all possible quantum states. In these equations, and are position and momentum probability density, respectively:
and corresponding waveforms and are related through the Fourier transformation:
Both of them satisfy orthonormality conditions:
where is a Kronecker delta, . Real position wave function and associated eigen energy En are found from the 1D Schrödinger equation:
with mp being a mass of the particle and V(x) being an external potential.
First, we point out that for the infinite potential well of the width a the Fisher informations were calculated before [4] where the position component was evaluated directly from equation (1a) whereas for finding an elegant and didactically instructive method was used; namely, since for this geometry both and are real, the integrand in equation (1b) becomes , and using the reciprocity between position and momentum spaces, equation (3), one replaces infinite p integration by the finite x one:
Turning to the discussion of the quasi-1D hydrogen atom, it has to be noted that a problem of the quantum motion along the whole x axis, , in the potential , despite its long history, still remains (owing to the strong singularity at the origin and concomitant difficulty of matching right and left solutions at x = 0) a topic of debate and controversy, see, e.g., [5, 6] and literature cited therein. A situation is somewhat simplified when one confines the motion only to the right half space terminated at x = 0 by the infinite barrier. Accordingly, let us consider solutions of the Schrödinger equation (5) with the potential [1]
. Upon introducing Coulomb units where energies and distances are measured in terms of and , respectively [7], and momenta—in units of , one arrives at the differential equation
whose general solution for the negative energies, , corresponding to the bound states, reads:
Here, and are Kummer, or confluent hypergeometric, functions (we follow the notation adopted in [8]), and c1 and c2 are normalisation constants. Physically, this mathematical solution vanishes at the origin and, since the second item in the square brackets of the right-hand side of equation (9) diverges at [8], it has to be neglected, . Remaining part must decay sufficiently fast at infinity. From the properties of the Kummer function [8] it follows that it is possible only when its first parameter is equal to the nonpositive integer what immediately leads to the energy spectrum coinciding with the 3D hydrogen atom [7]
whereas the corresponding waveform simplifies to
with , , being a generalised Laguerre polynomial [8]. Figure 1 shows waveforms of the first four levels. Didactically, a representation of the solution in the form of the Laguerre polynomials is much more advantageous compared to that of the confluent hypergeometric functions, equation (16) in [1]; in particular, utilising properties of the Laguerre polynomials (see equation 2.19.14.18 in [9]), one instantly confirms that equation (11) does satisfy the orthonormality condition, equation (4a), for .1 Moreover, the form of solution from equation (11) allows an instructive calculation from equation (3) of the momentum waveform. For doing this, one recalls Rodrigues formula for Laguerre polynomials [8]:
Then, becomes:
Successive integrations by parts simplify this to:
An elementary deformation of the integration contour in this equation yields ultimately:
Observe that this complex solution is completely different from the real one provided by equation (17) from [1]. With the help of residue theorem applied to calculation of the integrals with infinite limits [10], it is elementary to check that the set from equation (15) does obey equation (4b), as expected. The dependencies of the real and imaginary parts of the waveforms on the momentum are shown in figure 2. It is seen that the number and amplitude of the oscillations increase for the higher quantum indices n.
Download figure:
Standard image High-resolution imageKnowledge of the functions and and, accordingly, of the corresponding densities
paves the way to calculating the associated Fisher informations. Dropping quite simple intermediate computations (which in the case of the position component rely on the properties of the Laguerre polynomials [8, 9] while for its momentum counterpart elementary properties of the integrals of the product of the power and algebraic functions are employed), the ultimate results are given as
what leads to the index independent product
Note that position Fisher information whose expression, equation (17a), does coincide with its counterpart from [1] is proportional to the absolute value of energy what is its general property while the momentum component is just the inverse of . As a result, the product of the two informations stays the same for all levels. This n independence singles out the hydrogen atom from other two structures studied in [1] for which is a quadratic function of the quantum index.
Footnotes
- 1