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The Journal of Chemical Physics

Seniority eigenstate configuration interaction

Thomas M. Henderson, Guo P. Chen, Gustavo E. Scuseria

Published Jul 7, 2026• 0 citations
Publisher

Abstract

Zero-seniority methods have shown great promise for the description of strongly correlated electronic systems. Other seniority sectors have been much less explored, and in particular, the maximal seniority sector and zero seniority have the same underlying algebraic structure. We introduce a seniority eigenstate configuration interaction in which the wave function is constrained to have good fixed local seniority for each paired orbital, by which we mean we partition orbitals into a pairing set with seniority zero, and a spin set with seniority one. We show how to build the effective Hamiltonian for this ansatz, and demonstrate that high-seniority wave functions have unexpectedly excellent accuracy for strongly correlated fermionic systems, with accuracy competitive with or better than seniority zero for the Hubbard model and for the dissociation of the nitrogen molecule.

DOI
10.1063/5.0339766

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Physical Review C•May 11, 2007•23 citations
Zero-seniority methods have shown great promise for the description of strongly correlated electronic systems. Other seniority sectors have been much less explored, and in particular, the maximal seniority sector and zero seniority have the same underlying algebraic structure. We introduce a seniority eigenstate configuration interaction in which the wave function is constrained to have good fixed local seniority for each paired orbital, by which we mean we partition orbitals into a pairing set with seniority zero, and a spin set with seniority one. We show how to build the effective Hamiltonian for this ansatz, and demonstrate that high-seniority wave functions have unexpectedly excellent accuracy for strongly correlated fermionic systems, with accuracy competitive with or better than seniority zero for the Hubbard model and for the dissociation of the nitrogen molecule.
Zero-seniority methods have shown great promise for the description of strongly-correlated electronic systems. Other seniority sectors have been much less explored, and in particular the maximal seniority sector and zero seniority have the same underlying algebraic structure. We introduce a seniority eigenstate configuration interaction in which the wave function is constrained to have good fixed local seniority for each paired orbital, by which we mean we partition orbitals into a pairing set with seniority zero, and a spin set with seniority one. We show how to build the effective Hamiltonian for this ansatz, and demonstrate that high-seniority wave functions have unexpectedly excellent accuracy for strongly-correlated fermionic systems, with accuracy competitive with or better than seniority zero for the Hubbard model and for the dissociation of the nitrogen molecule.
Seniority is a useful way of organizing Hilbert space for strongly correlated systems. The exact zero-seniority wave function, doubly occupied configuration interaction (DOCI), provides accurate results (given the right orbitals) for many strongly correlated electronic systems but has a combinatorial computational cost. In many cases, pair coupled cluster doubles provide a polynomial-cost approximation that closely reproduces the energies of DOCI, but it breaks down in some cases and, as shown herein, it does not provide particularly good density matrices. In this work, we demonstrate that by using the Jordan-Wigner transformation to turn the seniority zero problem back into a Fermionic one, we can provide mean-field variational results of DOCI quality for the Hubbard model and a few small molecular dissociation examples, with polynomial cost, both for the energies and for density matrices, all while being protected from collapse. This success is rooted in the proof we provide, showing that the Hartree-Fock wave function on the Jordan-Wigner-transformed Hamiltonian transforms back to variational coupled cluster doubles in the seniority zero representation, but restricted to have determinant rather than permanent amplitude coefficients, without compromising its overall accuracy.
Single reference treatment of strongly correlated H4_44​ and H10_{10}10​ isomers with Richardson-Gaudin states
Richardson-Gaudin (RG) states are employed as a variational wavefunction ansatz for strongly correlated isomers of H4_44​ and H10_{10}10​. In each case a single RG state describes the seniority-zero sector quite well. Simple natural orbital functionals offer a cheap and reasonable approximation of the outstanding weak correlation in the seniority-zero sector, while systematic improvement is achieved by performing a configuration interaction (CI) in terms of RG states. Other pair theories (e.g. generalized valence bond and pair-coupled-cluster doubles) can provide a good description of many of the geometries considered, but, at short distances, the wavefunctions for the 2D and 3D structures of H10_{10}10​ take the form of an RG state that cannot be described by these other theories.
We introduce a novel class of coupled cluster (CC) methods that leverage the seniority concept to enhance efficiency and accuracy in electronic structure calculations. While existing approaches, such as the pair coupled cluster doubles (pCCD) method, are limited to seniority-zero (Ω = 0) wavefunctions,1 we propose a more flexible framework: seniority-restricted coupled cluster (sr-CC). This new methodology selectively constrains the seniority sectors accessible through excitation operators in the cluster expansion, enabling a more systematic exploration of electron correlation effects. By balancing computational cost and accuracy, sr-CC provides a promising pathway for advancing electronic structure theory, particularly in strongly correlated systems.
The lowest seniority-zero eigenstates of an exactly solvable multilevel pairing Hamiltonian for a finite Fermi system are examined at different pairing regimes. After briefly reviewing the form of the eigenstates in the Richardson formalism, we discuss a different representation of these states in terms of the collective pairs resulting from the diagonalization of the Hamiltonian in a space of two degenerate time-reversed fermions. We perform a two-fold analysis by working both in the fermionic space of these collective pairs and in a space of corresponding elementary bosons. On the fermionic side, we monitor the variations which occur, with increasing the pairing strength, in the structure of both these collective pairs and the lowest eigenstates. On the bosonic side, after reviewing a fermion-boson mapping procedure, we construct exact images of the fermion eigenstates and study their wave function. The analysis allows a close examination of the phenomenon of pair condensation in a finite Fermi system and gives new insights into the evolution of the lowest (seniority-zero) excited states of a pairing Hamiltonian from the unperturbed regime up to a strongly interacting one.