In quantum chemistry and physics, the Lieb–Oxford inequality provides a lower bound for the indirect part of the Coulomb energy of a quantum mechanical system. It is named after Elliott H. Lieb and Stephen Oxford.
In classical physics, one can calculate the Coulomb energy of a configuration of charged particles in the following way. First, calculate the charge density ρ, where ρ is a function of the coordinates x ∈ ℝ3. Second, calculate the Coulomb energy by integrating:
In other words, for each pair of points x and y, this expression calculates the energy related to the fact that the charge at x is attracted to or repelled from the charge at y. The factor of 1⁄2 corrects for double-counting the pairs of points.
In quantum mechanics, it is also possible to calculate a charge density ρ, which is a function of x ∈ ℝ3. More specifically, ρ is defined as the expectation value of charge density at each point. But in this case, the above formula for Coulomb energy is not correct, due to exchange and correlation effects. The above, classical formula for Coulomb energy is then called the "direct" part of Coulomb energy. To get the actual Coulomb energy, it is necessary to add a correction term, called the "indirect" part of Coulomb energy. The Lieb–Oxford inequality concerns this indirect part. It is relevant in density functional theory, where the expectation value ρ plays a central role.
Statement of the inequality
For a quantum mechanical system of N particles, each with charge e, the N-particle density is denoted by
The function P is only assumed to be non-negative and normalized. Thus the following applies to particles with any "statistics". For example, if the system is described by a normalised square integrable N-particle wave function
More generally, in the case of particles with spin having q spin states per particle and with corresponding wave function
the N-particle density is given by
Alternatively, if the system is described by a density matrix γ, then P is the diagonal
The electrostatic energy of the system is defined as
For x ∈ ℝ3, the single particle charge density is given by
and the direct part of the Coulomb energy of the system of N particles is defined as the electrostatic energy associated with the charge density ρ, i.e.
The Lieb–Oxford inequality states that the difference between the true energy IP and its semiclassical approximation D(ρ) is bounded from below as
where C ≤ 1.68 is a constant independent of the particle number N. EP is referred to as the indirect part of the Coulomb energy and in density functional theory more commonly as the exchange plus correlation energy. A similar bound exists if the particles have different charges e1, ... , eN. No upper bound is possible for EP.
The optimal constant
While the original proof yielded the constant C = 8.52, Lieb and Oxford managed to refine this result to C = 1.68. Later, the same method of proof was used to further improve the constant to C = 1.64. With these constants the inequality holds for any particle number N.
The constant can be further improved if the particle number N is restricted. In the case of a single particle N = 1 the Coulomb energy vanishes, IP = 0, and the smallest possible constant can be computed explicitly as C1 = 1.092. The corresponding variational equation for the optimal ρ is the Lane–Emden equation of order 3. For two particles (N = 2) it is known that the smallest possible constant satisfies C2 ≥ 1.234. In general it can be proved that the optimal constants CN increase with the number of particles, i.e. CN ≤ CN + 1, and converge in the limit of large N to the best constant CLO in the inequality (1). Any lower bound on the optimal constant for fixed particle number N is also a lower bound on the optimal constant CLO. The best numerical lower bound was obtained for N = 60 where C60 ≥ 1.41. This bound has been obtained by considering an exponential density. For the same particle number a uniform density gives C60 ≥ 1.34.
The largest proved lower bound on the best constant is CLO ≥ 1.4442. It has been obtained in using a uniform electron gas, melted in the neighborhood of its surface. The same lower bound CLO ≥ 1.4442 had been proved earlier in, and acknowledged as such in. Hence, to summarise, the best known bounds for C are 1.44 ≤ C ≤ 1.64.
The Dirac constant
Historically, the first approximation of the indirect part EP of the Coulomb energy in terms of the single particle charge density was given by Paul Dirac in 1930 for fermions. The wave function under consideration is
With the aim of evoking perturbation theory, one considers the eigenfunctions of the Laplacian in a large cubic box of volume |Λ| and sets
where χ1, ..., χq forms an orthonormal basis of ℂq. The allowed values of k ∈ ℝ3 are n/|Λ|1⁄3 with n ∈ ℤ3
+. For large N, |Λ|, and fixed ρ = N |e|/|Λ|, the indirect part of the Coulomb energy can be computed to be
with C = 0.93.
This result can be compared to the lower bound (1). In contrast to Dirac's approximation the Lieb–Oxford inequality does not include the number q of spin states on the right-hand side. The dependence on q in Dirac's formula is a consequence of his specific choice of wave functions and not a general feature.
The constant C in (1) can be made smaller at the price of adding another term to the right-hand side. By including a term that involves the gradient of a power of the single particle charge density ρ, the constant C can be improved to 1.45. Thus, for a uniform density system C ≤ 1.45.
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