Partition function: Difference between revisions

From SklogWiki
Jump to navigation Jump to search
No edit summary
No edit summary
Line 2: Line 2:
at temperature <math>T</math> is the normalization constant of the [[Boltzmann distribution]]
at temperature <math>T</math> is the normalization constant of the [[Boltzmann distribution]]
function, and therefore its expression is given by
function, and therefore its expression is given by
:<math> \left. Z \right.= {\mathrm {Tr}} \{ e^{-\beta H} \}</math>
where ''H'' is the [[Hamiltonian]], or as


:<math>Z(T)=\int \Omega(E)\exp(-E/k_BT)\,dE</math>,
:<math>Z(T)=\int \Omega(E)\exp(-E/k_BT)\,dE</math>,

Revision as of 14:21, 24 September 2007

The canonical ensemble partition function of a system in contact with a thermal bath at temperature T is the normalization constant of the Boltzmann distribution function, and therefore its expression is given by

Z=Tr{e−βH}

where H is the Hamiltonian, or as

Z(T)=∫Ω(E)exp(−E/kBT)dE,

where Ω(E) is the density of states with energy E and kB the Boltzmann constant. The symbol Z is from the German Zustandssumme meaning "sum over states".

Helmholtz energy function

The partition function of a system is related to the Helmholtz energy function through the formula

A=−kBTlogZ.

This connection can be derived from the fact that kBlogΩ(E) is the entropy of a system with total energy E. This is an extensive magnitude in the sense that, for large systems (i.e. in the thermodynamic limit, when the number of particles N→∞ or the volume V→∞), it is proportional to N or V. In other words, if we assume N large, then

kBlogΩ(E)=Ns(e),

where s(e) is the entropy per particle in the thermodynamic limit, which is a function of the energy per particle e=E/N. We can therefore write

Z(T)=N∫exp{N(s(e)−e/T)/kB}de.

Since N is large, this integral can be performed through steepest descent, and we obtain

Z(T)=Nexp{N(s(e0)−e0/kBT)},

where e0 is the value that maximizes the argument in the exponential; in other words, the solution to

s′(e0)=1/T.

This is the thermodynamic formula for the inverse temperature provided e0 is the mean energy per particle of the system. On the other hand, the argument in the exponential is

1kBT(TS(E0)−E0)=−AkBT

the thermodynamic definition of the Helmholtz energy function. Thus, when N is large,

A=−kBTlogZ(T).

Connection with thermodynamics

We have the aforementioned Helmholtz energy function,

A=−kBTlogZ(T)

we also have the internal energy, which is given by

U=kBT2∂logZ(T)∂T|N,V

and the pressure, which is given by

p=kBT∂logZ(T)∂V|N,T.

These equations provide a link between classical thermodynamics and statistical mechanics

See also