context | J∈N |
j∈{1,…,J} | |
range | Nj∈N |
context | Nmaxj∈N∪{∞} |
context | ZNj(β) sequences in Nj of canonical partition functions with length Nmaxj |
definiendum | Ξ(β,μ1,…,μJ):=∑Jj=1∑NmaxjNj=0 z(β,μj)Nj⋅ZNj(β) |
Here z denotes the fugacity. The quantity J denotes the number of different particle species to consider.
The above definition mirrors the classical microcanonical phase volume and the classical canonical partition function.
The summands z(β,μj)Nj⋅ZNj(β) can be viewed as canonical partition function where the distributions e−β HNj are shifted to e−β (HNj−μj Nj). Accordingly the meaning of the so called chemical potential μs is a package of energy associated with each given particle in the system.
The index j is attached to the particle number N as well as to the chemical potential μ and is always dropped if the system of interest deals with only a single sort of particle.
Important grand canonical partition functions in QM are those for bosons and fermions denoted Ξ+ and Ξ−, respectively. We only deal with one sort of particle, but introduce the index r which runs over different energy levels. Using the identities
∑NmaxN=0(eβ∑rμ)N⋅e−β∑rNεr
∑NmaxN=0(∏reβμ⋅e−βεr)N
=∏r∑NmaxN=0(e−β (εr−μ))N
={∏r11−e−β (εr−μ)if Nmax=∞∏r(1+e−β (εr−μ))if Nmax=1
where εr are the energy eigenvalues we obtain
Ξ±(β,μ)=∏r(1−(±1) eβ (εr−μ))−(±1) |
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When computing the Grand potential, one applies the log and the product becomes a sum. The particle number expectation value ⟨ˆN⟩=−∂∂μΩ for these systems are
⟨ˆN⟩±=∑r⟨ˆnr⟩± |
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with the partition into energy levels given by the Einstein-Bose resp. Fermi-Dirac distribution functions
⟨ˆnr⟩±∝1eβ (εr−μ)−(±1) |
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The ∝ expresses takes into account the possible multiplicity of states r,r′,⋅ with equal energy εr,εr′,….
The above derivation presupposes that the different energy values are given by the discretely indexed expressions of the form ∼Nε. This is the historical beginning of quantum mechaniscs.
Wikipedia: Partition function (statistical mechanics)