Particle in a spherically symmetric potential

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File:Atomic-orbital-clouds spd m0.png

Hydrogen atomic orbitals of different energy levels. The more opaque areas are where one is most likely to find an electron at any given time.

In quantum mechanics, a spherically symmetric potential is a system of which the potential only depends on the radial distance from the spherical center and a location in space. A particle in a spherically symmetric potential will behave accordingly to said potential and can therefore be used as an approximation, for example, of the electron in a hydrogen atom or of the formation of chemical bonds.<ref>Template:Cite journal</ref>

In the general time-independent case, the dynamics of a particle in a spherically symmetric potential are governed by a Hamiltonian of the following form:<math display="block">\hat{H} = \frac{\hat{p}^2}{2m_0} + V({r})</math> Here, <math>m_0</math> is the mass of the particle, <math>\hat{p}</math> is the momentum operator, and the potential <math>V(r)</math> depends only on the vector magnitude of the position vector, that is, the radial distance from the origin (hence the spherical symmetry of the problem).

To describe a particle in a spherically symmetric system, it is convenient to use spherical coordinates; denoted by <math>r</math>, <math>\theta</math> and <math>\phi</math>. The time-independent Schrödinger equation for the system is then a separable, partial differential equation. This means solutions to the angular dimensions of the equation can be found independently of the radial dimension. This leaves an ordinary differential equation in terms only of the radius, <math>r</math>, which determines the eigenstates for the particular potential, <math>V(r)</math>.

Structure of the eigenfunctions

If solved by separation of variables, the eigenstates of the system will have the form:<math display="block">\psi(r, \theta, \phi) = R(r)\Theta(\theta)\Phi(\phi) </math> in which the spherical angles <math> \theta </math> and <math> \phi </math> represent the polar and azimuthal angle, respectively. Those two factors of <math>\psi</math> are often grouped together as spherical harmonics, so that the eigenfunctions take the form: <math display="block">\psi(r, \theta, \phi) = R(r)Y_{\ell m}(\theta,\phi). </math>

The differential equation which characterises the function <math>R(r)</math> is called the radial equation.

Derivation of the radial equation

The kinetic energy operator in spherical polar coordinates is:<math display="block">\frac{\hat{p}^2}{2m_0} = -\frac{\hbar^2}{2m_0} \nabla^2 = - \frac{\hbar^2}{2m_0\,r^2} \left[ \frac{\partial}{\partial r} \left(r^2 \frac{\partial}{\partial r}\right) - \hat{L}^2 \right].</math>The spherical harmonics satisfy<math display="block"> \hat{L}^2 Y_{\ell m}(\theta,\phi)\equiv \left\{ -\frac{1}{\sin^2\theta} \left[ \sin\theta \frac{\partial}{\partial\theta} \left(\sin\theta \frac{\partial}{\partial\theta}\right) +\frac{\partial^2}{\partial \phi^2}\right]\right\} Y_{\ell m}(\theta,\phi) = \ell(\ell+1)Y_{\ell m}(\theta,\phi).</math> Substituting this into the Schrödinger equation we get a one-dimensional eigenvalue equation,<math display="block"> \frac{1}{r^2}\frac{d}{dr} \left(r^2\frac{dR}{dr}\right) - \frac{\ell(\ell+1)}{r^2} R + \frac{2m_0}{\hbar^2} \left[E-V(r)\right]R = 0.</math>This equation can be reduced to an equivalent 1-D Schrödinger equation by substituting <math>R(r) = u(r)/r</math>, where <math> u(r)</math> satisfies<math display="block"> {d^2 u \over dr^2} + \frac{2m_0}{\hbar^2} \left[E-V_{\mathrm{eff}}(r)\right] u = 0</math>which is precisely the one-dimensional Schrödinger equation with an effective potential given by<math display="block"> V_{\mathrm{eff}}(r) = V(r) + {\hbar^2 \ell(\ell+1) \over 2m_0r^2},</math>where <math>r \in [0,\infty)</math>. The correction to the potential V(r) is called the centrifugal barrier term.

If <math display="inline">\lim_{r \to 0} r^2 V(r) =0</math>, then near the origin, <math>R \sim r^\ell</math>.

Spherically symmetric Hamiltonians

Since the Hamiltonian is spherically symmetric, it is said to be invariant under rotation, ie:

<math>{U(R)}^\dagger \hat{H} U(R)=\hat{H} </math>

Since angular momentum operators are generators of rotation, applying the Baker-Campbell-Hausdorff Lemma we get:

<math>{U(R)}^\dagger \hat{H} U(R) = e^{\frac{i\hat{n}\cdot \vec{L}\theta}{\hbar}} \hat{H} e^{\frac{-i\hat{n}\cdot \vec{L}\theta}{\hbar}} =\hat{H} + i\frac{\theta}{\hbar}\left[ \hat{n}\cdot \vec{L}, \hat{H}\right] +\frac 1 {2!}\left( i\frac{\theta}{\hbar}\right)^2\left[ \hat{n}\cdot \vec{L},\left[ \hat{n}\cdot \vec{L}, \hat{H}\right]\right] + \cdots = \hat H </math>

Since this equation holds for all values of <math> \theta </math>, we get that <math> [ \hat{n}\cdot \vec{L}, \hat{H}] =0 </math>, or that every angular momentum component commutes with the Hamiltonian.

Since <math> L_z </math> and <math> L^2 </math> are such mutually commuting operators that also commute with the Hamiltonian, the wavefunctions can be expressed as <math> |\alpha;\ell,m\rangle </math> or <math> \psi_{\alpha;\ell,m}(r,\theta,\phi) </math> where <math> \alpha </math> is used to label different wavefunctions.

Since <math display="inline"> L_\pm = L_x \pm i L_y </math> also commutes with the Hamiltonian, the energy eigenvalues in such cases are always independent of <math> m </math>.

<math display="block"> \hat H |\alpha; \ell,m\rangle = E_{\alpha; \ell}|\alpha; \ell,m\rangle </math>

Combined with the fact that <math display="inline"> L_\pm </math> differential operators only act on the functions of <math> \theta </math> and <math> \phi </math>, it shows that if the solutions are assumed to be separable as <math display="inline">\psi(r, \theta, \phi) = R(r) Y(\theta,\phi) </math>, the radial wavefunction <math>R(r)</math> can always be chosen independent of <math>m</math> values. Thus the wavefunction is expressed as:<ref>{{#invoke:citation/CS1|citation |CitationClass=web }}</ref>

<math display="block">\psi_{\alpha;\ell, m}(r, \theta, \phi) = R(r)_{\alpha;\ell}Y_{\ell m}(\theta,\phi). </math>

Solutions for potentials of interest

There are five cases of special importance:

1. <math>V(r) = 0</math>, or solving the vacuum in the basis of spherical harmonics, which serves as the basis for other cases.
2. <math>V(r)=V_0</math> (finite) for <math>r<r_0</math> and zero elsewhere.
3. <math>V(r) = 0</math> for <math>r < r_0</math> and infinite elsewhere, the spherical equivalent of the square well, useful to describe bound states in a nucleus or quantum dot.
4. <math>V(r) \propto r^{2}</math>for the three-dimensional isotropic harmonic oscillator.
5. <math>V(r) \propto \frac{1}{r}</math> to describe bound states of hydrogen-like atoms.

The solutions are outlined in these cases, which should be compared to their counterparts in cartesian coordinates, cf. particle in a box.

Vacuum case states

Let us now consider <math>V(r) = 0</math>. Introducing the dimensionless variables<math display="block">\rho\ \stackrel{\mathrm{def}}{=}\ kr, \qquad k\ \stackrel{\mathrm{def}}{=}\ \sqrt{2m_0E\over\hbar^2},</math>the equation becomes a Bessel equation for <math>J(\rho)\ \stackrel{\mathrm{def}}{=}\ \sqrt\rho R(r)</math>:<math display="block">\rho^2\frac{d^2 J}{d\rho^2}+\rho \frac{dJ}{d\rho}+\left[\rho^2-\left(\ell+\frac{1}{2}\right)^2 \right] J = 0</math>where regular solutions for positive energies are given by so-called Bessel functions of the first kind <math>J_{\ell+1/2}(\rho)</math> so that the solutions written for <math>R(r)</math> are the so-called spherical Bessel function

<math display="inline">R(r) = j_l(kr) \ \stackrel{\mathrm{def}}{=}\ \sqrt{\pi/(2kr)} J_{\ell+1/2}(kr)</math>.

The solutions of the Schrödinger equation in polar coordinates in vacuum are thus labelled by three quantum numbers: discrete indices ℓ and m, and k varying continuously in <math>[0,\infty)</math>:<math display="block">\psi(\mathbf{r}) = j_\ell(kr) Y_{\ell m}(\theta,\phi)</math>These solutions represent states of definite angular momentum, rather than of definite (linear) momentum, which are provided by plane waves <math>\exp(i \mathbf{k}\cdot\mathbf{r})</math>.

Sphere with finite "square" potential

Consider the potential <math>V(r)=V_0</math> for <math>r<r_0</math> and <math>V(r)=0</math> elsewhere - that is, inside a sphere of radius <math>r_0</math> the potential is equal to <math>V_0</math> and it is zero outside the sphere. A potential with such a finite discontinuity is called a square potential.<ref name ="Messiah">A. Messiah, Quantum Mechanics, vol. I, p. 78, North Holland Publishing Company, Amsterdam (1967). Translation from the French by G.M. Temmer</ref>

We first consider bound states, i.e. states which display the particle mostly inside the box (confined states). Those have an energy <math>E</math> less than the potential outside the sphere, i.e., they have negative energy. Also worth noticing is that unlike Coulomb potential, featuring an infinite number of discrete bound states, the spherical square well has only a finite (if any) number because of its finite range.

The resolution essentially follows that of the vacuum case above with normalization of the total wavefunction added, solving two Schrödinger equations — inside and outside the sphere — of the previous kind, i.e., with constant potential. The following constraints must hold for a normalizable, physical wavefunction:

1. The wavefunction must be regular at the origin.
2. The wavefunction and its derivative must be continuous at the potential discontinuity.
3. The wavefunction must converge at infinity.

The first constraint comes from the fact that Neumann and Hankel functions are singular at the origin. The physical requirement that <math>\psi</math> must be defined everywhere selected Bessel function of the first kind over the other possibilities in the vacuum case. For the same reason, the solution will be of this kind inside the sphere:<math display="block">R(r) = A j_\ell\left(\sqrt{\frac{2 m_0 (E-V_0)}{\hbar^2}}r\right), \qquad r < r_0.</math>Note that for bound states, <math>V_0 < E < 0</math>. Bound states bring the novelty as compared to the vacuum case now that <math>E<0</math>. This, along with the third constraint, selects the Hankel function of the first kind as the only converging solution at infinity (the singularity at the origin of these functions does not matter since we are now outside the sphere):<math display="block">R(r) = Bh^{(1)}_\ell\left(i\sqrt{\frac{-2 m_0 E}{\hbar^2}}r\right), \qquad r>r_0</math>The second constraint on continuity of <math>\psi</math> at <math>r=r_0</math> along with normalization allows the determination of constants <math>A</math> and <math>B</math>. Continuity of the derivative (or logarithmic derivative for convenience) requires quantization of energy.

Sphere with infinite "square" potential

In case where the potential well is infinitely deep, so that we can take <math>V_0=0</math> inside the sphere and <math>\infty</math> outside, the problem becomes that of matching the wavefunction inside the sphere (the spherical Bessel functions) with identically zero wavefunction outside the sphere. Allowed energies are those for which the radial wavefunction vanishes at the boundary. Thus, we use the zeros of the spherical Bessel functions to find the energy spectrum and wavefunctions. Calling <math>u_{\ell,k}</math> the k^th zero of <math>j_\ell</math>, we have:<math display="block">E_{kl} = \frac{u_{\ell,k}^2 \hbar^2}{2 m_0 r_0^2}</math>so that the problem is reduced to the computations of these zeros <math>u_{\ell,k}</math>, typically by using a table or calculator, as these zeros are not solvable for the general case.

In the special case <math>\ell = 0</math> (spherical symmetric orbitals), the spherical Bessel function is <math display="inline">j_0(x) = \frac{\sin x} {x}</math>, which zeros can be easily given as <math>u_{0,k} = k \pi</math>. Their energy eigenvalues are thus: <math display="block">E_{k0} = \frac{(k \pi)^2\hbar^2}{ 2 m_0 r_0^2} = \frac{k^2 h^2}{8 m_0 r_0^2}</math>

3D isotropic harmonic oscillator

The potential of a 3D isotropic harmonic oscillator is <math display="block"> V(r) = \frac{1}{2} m_0 \omega^2 r^2. </math> An N-dimensional isotropic harmonic oscillator has the energies <math display="block">E_n = \hbar \omega\left( n + \frac{N}{2} \right) \quad\text{with}\quad n=0,1,\ldots,\infty,</math> i.e., <math>n</math> is a non-negative integral number; <math>\omega</math> is the (same) fundamental frequency of the <math>N</math> modes of the oscillator. In this case <math>N=3</math>, so that the radial Schrödinger equation becomes, <math display="block">\left[-\frac{\hbar^2}{2m_0} \frac{d^2}{dr^2} + {\hbar^2 \ell(\ell+1) \over 2m_0r^2}+\frac{1}{2} m_0 \omega^2 r^2 - \hbar\omega\left(n+\tfrac{3}{2}\right) \right] u(r) = 0.</math>

Introducing <math display="block">\gamma \equiv \frac{m_0\omega}{\hbar}</math> and recalling that <math>u(r) = r R(r)</math>, we will show that the radial Schrödinger equation has the normalized solution, <math display="block">R_{n\ell}(r) = N_{n\ell} \, r^{\ell} \, e^{-\frac{1}{2}\gamma r^2}\; L^{\scriptscriptstyle\left(\ell+\frac{1}{2}\right)}_{\frac{1}{2}(n-\ell)}(\gamma r^2),</math> where the function <math>L^{(\alpha)}_k(\gamma r^2)</math> is a generalized Laguerre polynomial in <math>yr^2</math> of order <math>k</math>.

The normalization constant <math>N_{nl}</math> is, <math display="block"> N_{n\ell} = \left[\frac{ 2^{n+\ell+2} \,\gamma^{\ell+\frac{3}{2}} } {\pi^{\frac{1}{2}}} \right]^{\frac{1}{2}}

\left[\frac{ \left[\frac{1}{2} (n-\ell)\right]!\;\left[\frac{1}{2} (n+\ell)\right]!}{(n+\ell+1)!} \right]^{\frac{1}{2}} .</math>

The eigenfunction <math>R_{nl}(r)</math> is associated with energy <math>E_n</math>, where <math display="block"> \ell = n, n-2, \ldots, \ell_\min\quad \text{with}\quad \ell_\min = \begin{cases} 1 & \text{if}~ n~ \text{odd} \\ 0 & \text{if}~ n~ \text{even} \end{cases}</math> This is the same result as the quantum harmonic oscillator, with <math>\gamma = 2 \nu</math>.

Derivation

First we transform the radial equation by a few successive substitutions to the generalized Laguerre differential equation, which has known solutions: the generalized Laguerre functions. Then we normalize the generalized Laguerre functions to unity. This normalization is with the usual volume element Template:Math.

First we scale the radial coordinate <math display="block">y = \sqrt{\gamma}r \quad \text{with}\quad \gamma \equiv \frac{m_0\omega}{\hbar},</math> and then the equation becomes <math display="block">\left[\frac{d^2}{dy^2} - \frac{\ell(\ell+1)}{y^2} - y^2 + 2n + 3 \right] v(y) = 0 </math> with <math display="inline">v(y) = u \left(y / \sqrt{\gamma} \right)</math>.

Consideration of the limiting behavior of Template:Math at the origin and at infinity suggests the following substitution for Template:Math, <math display="block">v(y) = y^{\ell+1} e^{-y^2/2} f(y).</math> This substitution transforms the differential equation to <math display="block">\left[\frac{d^2}{dy^2} + 2 \left(\frac{\ell+1}{y}-y\right)\frac{d}{dy} + 2n - 2\ell \right] f(y) = 0,</math> where we divided through with <math>y^{\ell+1} e^{-y^2/2}</math>, which can be done so long as y is not zero.

Transformation to Laguerre polynomials

If the substitution <math>x = y^2</math> is used, <math>y = \sqrt{x}</math>, and the differential operators become <math display="block">\frac{d}{dy} = \frac{dx}{dy}\frac{d}{dx} = 2 y \frac{d}{dx} = 2 \sqrt{x} \frac{d}{dx},</math> and <math display="block">\frac{d^2}{dy^2} = \frac{d}{dy} \left( 2 y \frac{d}{dx} \right) = 4 x \frac{d^2}{dx^2} + 2 \frac{d}{dx}. </math>

The expression between the square brackets multiplying <math>f(y)</math> becomes the differential equation characterizing the generalized Laguerre equation (see also Kummer's equation): <math display="block">x\frac{d^2g}{dx^2} + \left( \left(\ell+\frac{1}{2}\right) + 1 - x\right) \frac{dg}{dx} + \frac{1}{2} (n - \ell) g(x) = 0</math> with <math>g(x) \equiv f(\sqrt{x}) </math>.

Provided <math>k \equiv (n-\ell)/2</math> is a non-negative integral number, the solutions of this equations are generalized (associated) Laguerre polynomials <math display="block"> g(x) = L_k^{\scriptscriptstyle\left(\ell+\frac{1}{2}\right)}(x).</math>

From the conditions on <math>k</math> follows: (i) <math>n \ge \ell</math> and (ii) <math>n</math> and <math>l</math> are either both odd or both even. This leads to the condition on <math>l</math> given above.

Recovery of the normalized radial wavefunction

Remembering that <math>u(r) = r R(r)</math>, we get the normalized radial solution: <math display="block">R_{n\ell}(r) = N_{n\ell} \, r^{\ell} \, e^{-\frac{1}{2}\gamma r^2}\; L^{\scriptscriptstyle\left(\ell+\frac{1}{2}\right)}_{\frac{1}{2}(n-\ell)}(\gamma r^2).</math>

The normalization condition for the radial wave function is: <math display="block">\int^\infty_0 r^2 |R(r)|^2 \, dr = 1.</math>

Substituting <math>q = \gamma r^2 </math>, gives <math>dq = 2 \gamma r \, dr</math> and the equation becomes: <math display="block">\frac{N^2_{n\ell}}{2\gamma^{\ell+\frac{3}{2}}} \int^\infty_0 q^{\ell + {1 \over 2}} e^{-q} \left [ L^{\scriptscriptstyle\left(\ell+\frac{1}{2}\right)}_{\frac{1}{2}(n-\ell)}(q) \right ]^2 \, dq = 1.</math>

By making use of the orthogonality properties of the generalized Laguerre polynomials, this equation simplifies to: <math display="block">\frac{N^2_{n\ell}}{2\gamma^{\ell+\frac{3}{2}}} \cdot \frac{\Gamma{\left[\frac{1}{2} (n+\ell+1)+1\right]}}{\left[\frac{1}{2}(n-\ell)\right]!} = 1.</math>

Hence, the normalization constant can be expressed as: <math display="block">N_{n\ell} = \sqrt{\frac{2 \, \gamma^{\ell+\frac{3}{2}} \, \left(\frac{n-\ell}{2}\right)! }{\Gamma{\left(\frac{n+\ell}{2}+\frac{3}{2}\right)}}} </math>

Other forms of the normalization constant can be derived by using properties of the gamma function, while noting that <math>n</math> and <math>l</math> are both of the same parity. This means that <math>n+l</math> is always even, so that the gamma function becomes: <math display="block">\Gamma \left[\frac{1}{2} + \left( \frac{n+\ell}{2} + 1 \right) \right] = \frac{\sqrt{\pi}(n+\ell+1)!!}{2^{\frac{n+\ell}{2}+1}} = \frac{\sqrt{\pi}(n+\ell+1)!}{2^{n+\ell+1}\left[\frac{1}{2}(n+\ell)\right]!},</math> where we used the definition of the double factorial. Hence, the normalization constant is also given by: <math display="block"> N_{n\ell} = \left [ \frac{2^{n+\ell+2} \,\gamma^{\ell+{3 \over 2}}\left[{1 \over 2}(n-\ell)\right]!\left[{1 \over 2}(n+\ell)\right]!}{\;\pi^{1 \over 2} (n+\ell+1)! } \right ]^{1 \over 2} = \sqrt{2} \left( \frac{\gamma}{\pi} \right )^{1 \over 4} \,({2 \gamma})^{\ell \over 2} \, \sqrt{\frac{2 \gamma (n-\ell)!!}{(n+\ell+1)!!}}.</math>

Hydrogen-like atoms

{{#invoke:Labelled list hatnote|labelledList|Main article|Main articles|Main page|Main pages}} A hydrogenic (hydrogen-like) atom is a two-particle system consisting of a nucleus and an electron. The two particles interact through the potential given by Coulomb's law: <math display="block">V(r) = -\frac{1}{4 \pi \varepsilon_0} \frac{Ze^2}{r}</math> where

• ε₀ is the permittivity of the vacuum,
• Z is the atomic number (eZ is the charge of the nucleus),
• e is the elementary charge (charge of the electron),
• r is the distance between the electron and the nucleus.

In order to simplify the Schrödinger equation, we introduce the following constants that define the atomic unit of energy and length:

<math display="block"> E_\textrm{h} = \mu \left( \frac{e^2}{4 \pi \varepsilon_0 \hbar}\right)^2 \quad\text{and}\quad a_0 = {{4\pi\varepsilon_0\hbar^2}\over{\mu e^2}}. </math>

where <math> \mu \approx m_e </math> is the reduced mass in the <math>m_e \ll m_{nucleus}</math> limit. Substitute <math> y = Zr/a_0</math> and <math>W = E/(Z^2 E_\textrm{h})</math> into the radial Schrödinger equation given above. This gives an equation in which all natural constants are hidden, <math display="block"> \left[ -\frac{1}{2} \frac{d^2}{dy^2} + \frac{1}{2} \frac{\ell(\ell+1)}{y^2} - \frac{1}{y}\right] u_\ell = W u_\ell .</math> Two classes of solutions of this equation exist:

(i) <math> W </math> is negative, the corresponding eigenfunctions are square-integrable and the values of <math> W </math> are quantized (discrete spectrum).

(ii) <math> W </math> is non-negative, every real non-negative value of <math> W </math> is physically allowed (continuous spectrum), the corresponding eigenfunctions are non-square integrable. Considering only class (i) solutions restricts the solutions to wavefunctions which are bound states, in contrast to the class (ii) solutions that are known as scattering states.

For class (i) solutions with negative W the quantity <math>\alpha \equiv 2\sqrt{-2W}</math> is real and positive. The scaling of <math> y </math>, i.e., substitution of <math>x \equiv \alpha y </math> gives the Schrödinger equation: <math display="block">\left[ \frac{d^2}{dx^2} -\frac{\ell(\ell+1)}{x^2} + \frac{2}{\alpha x} - \frac{1}{4} \right] u_\ell = 0, \quad \text{with } x \ge 0.</math>

For <math> x \rightarrow \infty</math> the inverse powers of x are negligible and the normalizable (and therefore, physical) solution for large <math> x </math> is <math>\exp[-x/2]</math>. Similarly, for <math> x \rightarrow 0</math> the inverse square power dominates and the physical solution for small <math> x </math> is x^ℓ+1. Hence, to obtain a full range solution we substitute <math display="block">u_l(x) = x^{\ell+1} e^{-x/2}f_\ell(x).</math>

The equation for <math> f_l(x) </math> becomes, <math display="block">\left[ x\frac{d^2}{dx^2} + (2\ell+2-x) \frac{d}{dx} +(n - \ell - 1)\right] f_\ell(x) = 0 \quad\text{with}\quad n = (-2W)^{-1/2}=\frac{2}{\alpha}.</math>

Provided <math>n-\ell-1</math> is a non-negative integer, this equation has polynomial solutions written as <math display="block"> L^{(2\ell+1)}_{k}(x),\qquad k=0,1,\ldots , </math> which are generalized Laguerre polynomials of order <math> k </math>. The energy becomes<math display="block"> W = -\frac{1}{2n^2}\quad \text{with}\quad n \equiv k+\ell+1 . </math>

The principal quantum number <math> n </math> satisfies <math> n \ge \ell+1</math>. Since <math>\alpha = 2/n</math>, the total radial wavefunction is <math display="block">R_{n\ell}(r) = \frac{u (r)}{r} = N_{n\ell} \left(\frac{2Zr}{n a_0}\right)^{\ell}\; e^{-{\tfrac{Zr}{n a_0}}}\; L^{(2\ell+1)}_{n-\ell-1}\left(\frac{2Zr}{n a_0}\right),</math> with normalization which absorbs extra terms from <math display="inline">\frac {1}{r}</math> <math display="block">N_{n\ell} = \left[\left(\frac{2Z}{n a_0}\right)^3 \cdot \frac{(n-\ell-1)!}{2n[(n+\ell)!]^3}\right]^{1 \over 2},</math> via<ref>H. Margenau and G. M. Murphy, The Mathematics of Physics and Chemistry, Van Nostrand, 2nd edition (1956), p. 130. Note that convention of the Laguerre polynomial in this book differs from the present one. If we indicate the Laguerre in the definition of Margenau and Murphy with a bar on top, we have <math>\bar{L}^{(k)}_{n+k} = (-1)^k (n+k)! L^{(k)}_n</math>.</ref>

<math display="block">\int_0^\infty x^{2\ell+2} e^{-x} \left[ L^{(2\ell+1)}_{n-\ell-1}(x)\right]^2 dx = \frac{2n (n+\ell)!}{(n-\ell-1)!} .</math>

The corresponding energy is <math display="block"> E = - \frac{Z^2}{2n^2}E_\textrm{h},\qquad n=1,2,\ldots . </math>

References

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