{ "id": "1505.04923", "version": "v1", "published": "2015-05-19T09:29:28.000Z", "updated": "2015-05-19T09:29:28.000Z", "title": "Quantum canonical ensemble: a projection operator approach", "authors": [ "Wim Magnus", "Fons Brosens" ], "comment": "14 pages, 3 figures", "categories": [ "cond-mat.stat-mech", "quant-ph" ], "abstract": "Fixing the number of particles $N$, the quantum canonical ensemble imposes a constraint on the occupation numbers of single-particle states. The constraint particularly hampers the systematic calculation of the partition function and any relevant thermodynamic expectation value for arbitrary $N$ since, unlike the case of the grand-canonical ensemble, traces in the $N$-particle Hilbert space fail to factorize into simple traces over single-particle states. In this paper we introduce a projection operator that enables a constraint-free computation of the partition function and its derived quantities, at the price of an angular or contour integration. Being applicable to both bosonic and fermionic non-interacting systems in arbitrary dimensions, the projection operator approach provides closed-form expressions for the partition function $Z_N$ and the Helmholtz free energy $F_{\\! N}$ as well as for two- and four-point correlation functions. While appearing only as a secondary quantity in the present context, the chemical potential potential emerges as a by-product from the relation $\\mu_N = F_{\\! N+1} - F_{\\! N}$, as illustrated for a two-dimensional fermion gas with $N$ ranging between 2 and 500.", "revisions": [ { "version": "v1", "updated": "2015-05-19T09:29:28.000Z" } ], "analyses": { "keywords": [ "projection operator approach", "quantum canonical ensemble", "partition function", "particle hilbert space fail", "single-particle states" ], "note": { "typesetting": "TeX", "pages": 14, "language": "en", "license": "arXiv", "status": "editable" } } }