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arXiv:2609.19535 · The Journal of Chemical Physics

Symmetry-driven correlation patterns in one-dimensional periodic fermionic systems: closed-form expressions and exact selection rules for correlation functions, entanglement entropies and mutual information

Celestino Angeli

quant-phSubmitted Sep 17, 2026• Announced Sep 18, 2026• 0 citations
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Abstract

We present an analytical study of the spatial structure of correlations in periodic fermionic systems at the single Slater determinant level, focusing on the cyclic case. Exploiting cyclic symmetry, the transformation from localized orbitals to molecular orbitals is simultaneously a discrete Fourier transform, a Vandermonde matrix on the roots of unity, a complex Hadamard matrix, and the character table of the cyclic group $C_m$. Within this framework, the spatial structure of correlations is fully determined by the occupied irreducible representations (Fourier modes), independently of the specific Hamiltonian generating them. In particular, the fermionic two-point correlator is expressed as a truncated Fourier sum over the occupied orbitals, leading to exact analytical expressions for symmetric occupation patterns of Fourier modes ($\ell$ and $-\ell$ pairs), corresponding in quantum chemistry to aromatic fillings, i.e. fillings satisfying Hückel's $4n + 2$ rule. For the half filling case, we derive exact spatial selection rules. In particular, the two-point correlator vanishes identically for all even distances along the ring. This property propagates to reduced density matrices and implies a complete absence of mutual information between the corresponding orbitals. These results reveal that, despite the global delocalization of molecular orbitals, the correlation structure in cyclic systems is highly non-uniform and governed by symmetry-induced interference. Although formulated in terms of cyclic lattice systems, the present results extend straightforwardly to one-dimensional fermionic chains with periodic conditions, reflecting the underlying translational symmetry of the problem. The framework therefore provides a Hamiltonian-independent and universal reference for understanding correlation patterns in one-dimensional periodic fermionic systems.

Journal reference
The Journal of Chemical Physics 165, 144110 (2026)
DOI
10.1063/5.0350248
Comments
The following article has been accepted by The Journal of Chemical Physics

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We present an analytical study of the spatial structure of correlations in periodic fermionic systems at the single Slater determinant level, focusing on the cyclic case. Exploiting cyclic symmetry, the transformation from localized orbitals to molecular orbitals is simultaneously a discrete Fourier transform, a Vandermonde matrix on the roots of unity, a complex Hadamard matrix, and the character table of the cyclic group CmC_mCm​. Within this framework, the spatial structure of correlations is fully determined by the occupied irreducible representations (Fourier modes), independently of the specific Hamiltonian generating them. In particular, the fermionic two-point correlator is expressed as a truncated Fourier sum over the occupied orbitals, leading to exact analytical expressions for symmetric occupation patterns of Fourier modes (ℓ\ellℓ and −ℓ-\ell−ℓ pairs), corresponding in quantum chemistry to aromatic fillings, i.e. fillings satisfying Hückel's 4n+24n + 24n+2 rule. For the half filling case, we derive exact spatial selection rules. In particular, the two-point correlator vanishes identically for all even distances along the ring. This property propagates to reduced density matrices and implies a complete absence of mutual information between the corresponding orbitals. These results reveal that, despite the global delocalization of molecular orbitals, the correlation structure in cyclic systems is highly non-uniform and governed by symmetry-induced interference. Although formulated in terms of cyclic lattice systems, the present results extend straightforwardly to one-dimensional fermionic chains with periodic conditions, reflecting the underlying translational symmetry of the problem. The framework therefore provides a Hamiltonian-independent and universal reference for understanding correlation patterns in one-dimensional periodic fermionic systems.
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We analyze the problem of quantifying entanglement in pure and mixed states of fermionic systems with a fixed number parity yet not necessarily a fixed particle number. The mode entanglement between one single-particle level and its orthogonal complement is first considered, and an entanglement entropy for such a partition of a particular basis of the single-particle Hilbert space H\mathcal{H}H is defined. The sum over all single-particle modes of this entropy is introduced as a measure of the total entanglement of the system with respect to the chosen basis and it is shown that its minimum over all bases of H\mathcal{H}H is a function of the one-body density matrix. Furthermore, we show that if minimization is extended to all bases related through a Bogoliubov transformation, then the entanglement entropy is a function of the generalized one-body density matrix. These results are then used to quantify entanglement in fermion systems with four single-particle levels. For general pure states of such a system a closed expression for the fermionic concurrence is derived, which generalizes the Slater correlation measure defined by J. Schliemann et al. [Phys. Rev. A 64, 022303 (2001)], implying that particle entanglement may be seen as minimum mode entanglement. It is also shown that the entanglement entropy defined before is related to this concurrence by an expression analogous to that in the two-qubit case. For mixed states of this system the convex roof extension of the previous concurrence and entanglement entropy is evaluated analytically, extending the results in previous reference to general states.
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