Quantum Mechanics, Volume 3. Claude Cohen-Tannoudji
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As we now show, the following relation is always true:
We first note that the function x lnx, defined for x ≥ 0, is always larger than the function x – 1, which is the equation of its tangent at x = 1 (Fig. 1). For positive values of x and y we therefore always have:
(9)
or, after multiplying by y:
the equality occurring only if x = y.
Figure 1: Plot of the function x lnx. At x = 1, this curve is tangent to the line y = x – 1 (dashed line) but always remains above it; the function value is thus always larger than x – 1.
Let us call pn the eigenvalues of ρ corresponding to the normalized eigenvectors |un〉, and
We now multiply this relation by the square of the modulus of the scalar product:
and sum over m and n. For the term in pn lnpn of (11), the summation over m yields in (12) the identity operator expanded on the basis {|vm〉}; we then get 〈un|un〉 = 1, and are left with the sum over n of pn lnpn, that is the trace Tr{ρ lnρ}. As for the term in pn ln
(13)
and we get:
(14)
As for the terms on the right-hand side of inequality (11), the term in pn yields:
(15)
and the one in
which proves (8).
Comment:
One may wonder under which conditions the above relation becomes an equality. This requires the inequality (11) to become an equality, which means
1-c. Minimization of the thermodynamic potential
The entropy S associated with any density operator ρ having a trace equal to 1 is defined by relation (6) of Appendix VI:
(17)
The thermodynamic potential of the grand canonical ensemble is defined by the “grand potential” Φ, which can be expressed as a function of ρ by relation (Appendix VI, § 1-c-β):
Inserting (5) into (18), we see that the value of Φ at equilibrium, Φeq, can be directly obtained from the partition function Z:
(19)
We therefore have:
Consider now any density operator ρ and its associated function Φ obtained from (18).