Grand canonical ensemble: Difference between revisions

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* <math> \left( R^*\right)^{3N} </math> represent the <math>3N</math> position coordinates of the particles (reduced with the system size): i.e. <math> \int d (R^*)^{3N} = 1 </math>
* <math> \left( R^*\right)^{3N} </math> represent the <math>3N</math> position coordinates of the particles (reduced with the system size): i.e. <math> \int d (R^*)^{3N} = 1 </math>


== Helmholtz energy and Partition Function ==
== Helmholtz energy and partition function ==
The  corresponding thermodynamic potential for the [[Grand canonical partition function | grand canonical partition function]] is:
The  corresponding thermodynamic potential for the [[Grand canonical partition function | grand canonical partition function]] is:


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:<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>


where ''A'' is the [[Helmholtz energy function]].
[[Category:Statistical mechanics]]
[[Category:Statistical mechanics]]

Revision as of 15:28, 5 March 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

Helmholtz energy and partition function

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

A−μN,

i.e.:

pV=kBTlogQμVT

where A is the Helmholtz energy function.