Grand canonical ensemble: Difference between revisions

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== Free energy and Partition Function ==
== Free energy and Partition Function ==


(THis subsection should be checked)
(This subsection should be checked)


The  corresponding thermodynamic potentail for the [[Grand canonical partition function | grand canonical partition function]] is:
The  corresponding thermodynamic potentail for the [[Grand canonical partition function | grand canonical partition function]] is:


: <math> \left. A - \mu N \right. </math>, i.e.:
: <math> \left. A - \mu N \right. </math>,  


i.e.:


:<math> \left. p V = k_B T \log Q_{\mu V T } \right. </math>
:<math> \left. p V = k_B T \log Q_{\mu V T } \right. </math>


[[Category:Statistical mechanics]]
[[Category:Statistical mechanics]]

Revision as of 14:51, 28 February 2007

Ensemble variables

  • Chemical Potential, μ
  • Volume, V
  • Temperature, T

Partition Function

Classical partition function (one-component system) in a three-dimensional space: QμVT

QμVT=∑N=0∞exp[βμN]VNN!Λ3N∫d(R*)3Nexp[−βU(V,(R*)3N)]

where:

  • N is the number of particles
  • U is the potential energy, which depends on the coordinates of the particles (and on the interaction model)
  • (R*)3N represent the 3N position coordinates of the particles (reduced with the system size): i.e. ∫d(R*)3N=1

Free energy and Partition Function

(This subsection should be checked)

The corresponding thermodynamic potentail for the grand canonical partition function is:

A−μN,

i.e.:

pV=kBTlogQμVT