Thermodynamics of quantum oscillators
Fuente:
arXiv
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| Formato: | Preprint |
| Publicado: |
2025
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| _version_ | 1866918085076713472 |
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| author | Caffarel, Michel |
| author_facet | Caffarel, Michel |
| contents | In this work, we present a compact analytical approximation for the quantum partition function of systems composed of quantum oscillators. The proposed formula is general and applicable to an arbitrary number of oscillators described by a rather general class of potential energy functions (not necessarily polynomials). Starting from the exact path integral expression of the partition function, we introduce a time-dependent Gaussian approximation for the potential contribution and, then, invoke a principle of minimal sensitivity to minimize the error. This leads to a system of coupled nonlinear equations whose solution yields the optimal parameters of the gaussian approximation. The resulting approximate partition function accurately reproduces thermodynamic quantities such as the free energy, average energy, and specific heat -- even at zero temperature -- with typical errors of only a few percent. We illustrate the performance of our approximate formula with numerical results for systems of up to ten coupled anharmonic oscillators. These results are compared to "exact" numerical results obtained via Hamiltonian diagonalization for small systems and Path Integral Monte Carlo simulations for larger ones. |
| format | Preprint |
| id |
arxiv_https___arxiv_org_abs_2507_04268 |
| institution | arXiv |
| publishDate | 2025 |
| record_format | arxiv |
| spellingShingle | Thermodynamics of quantum oscillators Caffarel, Michel Statistical Mechanics Chemical Physics In this work, we present a compact analytical approximation for the quantum partition function of systems composed of quantum oscillators. The proposed formula is general and applicable to an arbitrary number of oscillators described by a rather general class of potential energy functions (not necessarily polynomials). Starting from the exact path integral expression of the partition function, we introduce a time-dependent Gaussian approximation for the potential contribution and, then, invoke a principle of minimal sensitivity to minimize the error. This leads to a system of coupled nonlinear equations whose solution yields the optimal parameters of the gaussian approximation. The resulting approximate partition function accurately reproduces thermodynamic quantities such as the free energy, average energy, and specific heat -- even at zero temperature -- with typical errors of only a few percent. We illustrate the performance of our approximate formula with numerical results for systems of up to ten coupled anharmonic oscillators. These results are compared to "exact" numerical results obtained via Hamiltonian diagonalization for small systems and Path Integral Monte Carlo simulations for larger ones. |
| title | Thermodynamics of quantum oscillators |
| topic | Statistical Mechanics Chemical Physics |
| url | https://arxiv.org/abs/2507.04268 |