KMS state

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Kubo–Martin–Schwinger condition as featured on a monument in front of Warsaw University's Centre of New Technologies

In the statistical mechanics of quantum mechanical systems and quantum field theory, the properties of a system in thermal equilibrium can be described by a mathematical object called a Kubo–Martin–Schwinger (KMS) state: a state satisfying the KMS condition.

thermodynamic Green's functions,[2] and Rudolf Haag, Marinus Winnink and Nico Hugenholtz used the condition in 1967 to define equilibrium states and called it the KMS condition.[3]

Overview

The simplest case to study is that of a finite-dimensional Hilbert space, in which one does not encounter complications like phase transitions or spontaneous symmetry breaking. The density matrix of a thermal state is given by

where H is the Hamiltonian operator and N is the particle number operator (or charge operator, if we wish to be more general) and

is the

conserved
.

In the Heisenberg picture, the density matrix does not change with time, but the operators are time-dependent. In particular, translating an operator A by τ into the future gives the operator

.

A combination of

internal symmetry
"rotation" gives the more general

A bit of algebraic manipulation shows that the expected values

for any two operators A and B and any real τ (we are working with finite-dimensional Hilbert spaces after all). We used the fact that the density matrix commutes with any function of (H − μN) and that the trace is cyclic.

As hinted at earlier, with infinite dimensional Hilbert spaces, we run into a lot of problems like phase transitions, spontaneous symmetry breaking, operators that are not trace class, divergent partition functions, etc..

The

complex functions
of z, converges in the complex strip whereas converges in the complex strip if we make certain technical assumptions like the
spectrum of H − μN is bounded from below and its density does not increase exponentially (see Hagedorn temperature). If the functions converge, then they have to be analytic
within the strip they are defined over as their derivatives,

and

exist.

However, we can still define a KMS state as any state satisfying

with and being analytic functions of z within their domain strips.

and are the boundary distribution values of the analytic functions in question.

This gives the right large volume, large particle number thermodynamic limit. If there is a phase transition or spontaneous symmetry breaking, the KMS state is not unique.

The density matrix of a KMS state is related to

internal symmetry transformation for nonzero chemical potentials) via the Tomita–Takesaki theory
.

See also

References