Search arXivSearch

arXiv · 2109.12214

Analysis of Different Sets of Spin-Adapted Substitution Operators in Open-Shell Coupled Cluster Theory

Abstract

In spin-adapted open-shell coupled cluster (CC) theory, the choice of spin-free spatial substitution operators is generally not unique. Due to an increasing linear dependence of the cluster operator (with increasing substitution level), the options to span identical linear spaces increase rapidly. In this work several sets of non-orthogonal as well as orthogonal spin-adapted substitution operators are generated and used in consecutive Configuration Interaction (CI) and CC calculations. All (full) operator sets were generated to span the same linear space. The results are analyzed in terms of the produced wave function quality and the amount of recovered correlation energy w.r.t. full CI. In particular, the influence of different amounts of spectators, the influence of orthogonality as well as the effect of spin incompleteness was investigated. It was found that CC calculations involving fewer spectators lead to more accurate results in general. Here correlation energy differences of up to 0.32\% for minimal to maximal spectating sets were obtained. As expected, all conducted calculations led to identical results for non-orthogonal and orthogonal operator sets. Spin completeness on the other hand was found to be of great importance. Spin-incomplete Cluster operators led to significant errors in both the correlation energies and the FCI overlap.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Nils Herrmann, Michael Hanrath. 2021-09-24. Analysis of Different Sets of Spin-Adapted Substitution Operators in Open-Shell Coupled Cluster Theory. https://doi.org/10.1080/00268976.2021.2005836

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

KEEP EXPLORING

Related papers

Construction of downfolded Hamiltonians from projective transcorrelation

Projective transcorrelation recovers the short-range electron correlation by a similarity transformation with a geminal function $f(r_{12})$, at the cost of an effective Hamiltonian containing a 3-body term. We replace the term by an effective operator of rank at most two, obtained from the two-body cumulant (2C) approximation to the three-particle reduced density matrix. The 2C 3-body energy is written without cumulants, and the effective one- and two-body interactions are derived as its partial derivatives with respect to the reduced density matrices. The truncation is assessed on the atomization and reaction energies of the HEAT set with CCSD(T), and on the CAS-pTC model, whose downfolded Hamiltonian is held on a qubit register with the number of Pauli strings reduced from the sixth power of the orbital count to the fourth.

physics.chem-ph

Competing Ring-Opening and Hofmann Elimination Pathways in Aqueous TEMPO Catholytes: A First-Principles Study

Aqueous redox-flow batteries based on TEMPO derivatives are promising for large-scale energy storage, but their practical use is limited by the chemical instability of the oxidized N -oxoammonium state. In this work, we investigate the degradation of five TEMPO derivatives using ab initio molecular dynamics combined with enhanced sampling. Two proposed degradation mechanisms, ring opening and Hofmann elimination, are examined and their corresponding activation free energies are compared. For all derivatives considered, ring opening exhibits a lower activation free energy than Hofmann elimination, identifying it as the kinetically preferred degradation pathway. The magnitude of the ring-opening barrier, however, varies significantly between molecules, showing that different functionalizations strongly influence its stability toward degradation. The predicted preference for ring opening is consistent with available experimental studies, which have identified or inferred ring-opening degradation for several TEMPO-based catholytes. These results provide an atomistic picture of degradation pathways that are difficult to resolve experimentally and highlight the importance of molecular structure in controlling the kinetic stability of TEMPO derivatives in aqueous electrolytes.

physics.chem-ph

Exchange-Correlation Potentials and Energies from Inverse Generalized Kohn-Sham Calculations

The Kohn-Sham (KS) formulation of density functional theory (DFT) is a map from the many-electron problem to an effective single-electron problem that is governed by a local multiplicative potential. The generalized-Kohn-Sham (GKS) formalism extends it to permit any single-electron operator---nonlocal, local non-multiplicative, local multiplicative, or any combination of them. Doing so expands the scope and ease of modeling the exchange-correlation (XC) functional in DFT, which encodes the complicated many-electron interactions into a mean-field of the electron density. However, unlike KS theory, development of XC functionals in GKS theory has been hindered by the absence of corresponding exact XC potentials and energies. We present the exact XC potentials and energies for atoms and molecules by solving the inverse GKS problem, using highly accurate correlated \textit{ab initio} densities. Our approach is validated across weakly and strongly correlated systems. We further examine a common, yet untested, assumption that KS and GKS correlation potentials and energies are similar, finding instead that they differ substantially in strongly correlated systems. Overall, this work offers a powerful tool to model next-generation of XC functionals within the GKS formalism of DFT.

physics.chem-ph