Search arXivSearch

arXiv · 2601.16646

Algebraic Geometry for Spin-Adapted Coupled Cluster Theory

Abstract

We develop and numerically analyze an algebraic-geometric framework for spin-adapted coupled-cluster (CC) theory. Since the electronic Hamiltonian is SU(2)-invariant, physically relevant quantum states lie in the spin singlet sector. We give an explicit description of the SU(2)-invariant (spin singlet) many-body space by identifying it with an Artinian commutative ring, called the excitation ring, whose dimension is governed by a Narayana number. We define spin-adapted truncation varieties via embeddings of graded subspaces of this ring, and we identify the CCS truncation variety with the Veronese square of the Grassmannian. Compared to the spin-generalized formulation, this approach yields a substantial reduction in dimension and degree, with direct computational consequences. In particular, the CC degree of the truncation variety -- governing the number of homotopy paths required to compute all CC solutions -- is reduced by orders of magnitude. We present scaling studies demonstrating asymptotic improvements and we exploit this reduction to compute the full solution landscape of spin-adapted CC equations for water and lithium hydride.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Fabian M. Faulstich, Svala Sverrisdóttir. 2026-02-05. Algebraic Geometry for Spin-Adapted Coupled Cluster Theory. https://arxiv.org/abs/2601.16646

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related papers

Intrinsic Matching Frustration in Fluctuating Finite Systems

We formulate intrinsic matching frustration (IMF), a fluctuation-induced, kinetics-independent reduction in the mean capacity permitted by a prescribed matching rule. For complementary one-to-one matching, the instantaneous capacity is set by the minority population, so fluctuations produce a nonzero mean deficit even when the two populations are balanced on average. At finite size, this deficit depends on the full distribution of the population difference and is determined by its variance alone only in the Gaussian limit. Compartmentalization hides matching capacity by preventing cancellation between local imbalances of opposite sign. Fusion releases this hidden capacity monotonically under coarse graining, producing a measurable recovery of product yield following local reaction to completion.

physics.chem-ph

Phonon chirality as an additive control of CISS: a symmetry-protected law

Chirality-induced spin selectivity (CISS) is usually associated with molecular handedness. The possible contribution of chiral phonons is less established. We study a helical tight-binding model in which local phonon angular momentum modulates spin-dependent nearest-neighbor hopping. Fewest-switches surface hopping calculations give the transmitted spin polarization $\mathrm{SP}=aC+b\mathrm{PH}$. Here $C$ is the molecular chirality and $\mathrm{PH}$ is the phonon chirality. A mirror symmetry reverses $C$, $\mathrm{PH}$, and $\mathrm{SP}$ simultaneously. This symmetry excludes both a chirality-independent offset and a $C\cdot\mathrm{PH}$ term. The phonon contribution can therefore enhance, cancel, or reverse the molecular CISS signal.

physics.chem-ph

A fast physics-based matrix model for the impedance of a PEM fuel cell: Incorporating functionally graded catalyst layer and channel impedances

We extend a recent physics-based matrix model for calculating PEM fuel cell impedance (doi:10.1149/2754-2734/ad6ce8) to cases of low air flow stoichiometry and functionally graded cathode catalyst layers (CCLs). We demonstrate that the matrix model produces accurate spectra and is almost three orders of magnitude faster than a model based on the standard boundary-value problem solver. The physics-based matrix model can compete with equivalent circuit models for fitting experimental EIS spectra, particularly those measured from cells with functionally graded CCL.

physics.chem-ph