arXiv subjects

Kaila E. Weflen

Publications and source records attributed to Kaila E. Weflen.

3 recordsLinked to original sources

arXiv2026

Toward an affordable density-based measure for the quality of a coupled cluster calculation

We propose two new diagnostics for the degree to which static correlation impacts the quality of a coupled cluster calculation. The first is the change in the Matito static correlation diagnostic $\overline{I_{ND}}$ between CCSD and CCSD(T), $ΔI_{ND}[\textrm{(T)}]=\overline{I_{ND}}[\textrm{CCSD(T)}]-\overline{I_{ND}}[\textrm{CCSD}]$. The second is the ratio of the same and of the corresponding change in the total correlation diagnostic $\overline{I_{T}}=\overline{I_{ND}}+\overline{I_{D}}$, i.e., $r_I[(T)]=ΔI_{ND}[\textrm{(T)}]/ΔI_{T}[\textrm{(T)}]$. The first diagnostic can be extended to higher-order improvements in the wave function, e.g., $ΔI_{ND}[\textrm{(Q)}]=\overline{I_{ND}}[\textrm{CCSDT(Q)}]-\overline{I_{ND}}[\textrm{CCSDT}]$. In general, a small $ΔI_{ND}$[\textrm{level$_1$}] value indicates that at this level$_1$ of theory, the density is converged and any further changes to the energy come from dynamical correlation, while larger $ΔI_{ND}$[\textrm{level$_2$}] indicates that the density is still not converged at level$_2$ and some static correlation remains. $r_I[(T)]$ is found to be a moderately good predictor for the importance of post-CCSD(T) correlation effects.

physics.chem-ph↗

arXiv2026

Coupling between thermochemical contributions of subvalence correlation and of higher-order post-CCSD(T) correlation effects -- a step toward `W5 theory'

We consider the thermochemical impact of post-CCSD(T) contributions to the total atomization energy (TAE, the sum of all bond energies) of first- and second-row molecules, and specifically their coupling with the subvalence correlation contribution. In particular, we find large contributions from (Q) when there are several neighboring second-row atoms. Otherwise, both higher-order triples $T_3$--(T) and connected quadruples (Q) are important in systems with strong static correlation. Reoptimization of the reference geometry for core-valence correlation increases the calculated TAE across the board, most pronouncedly so for second-row compounds with neighboring second-row atoms. %just slightly increases the calculated TAE for all species, but more pronouncedly so if strong static correlation is present, as well as for second-row compounds, again especially with neighboring second-row atoms. We present a first proposal for a `W5 theory' protocol and compare computed TAEs for the W4-08 benchmark with prior reference values. For some key second-row species, the new values represent nontrivial revisions. Our predicted TAE$_0$ values (TAE at 0 K) agree well with the ATcT (active thermochemical tables) values, including for the very recent expansion of the ATcT network to boron, silicon, and sulfur compounds.

physics.chem-ph↗

arXiv2025

Exploiting a Shortcoming of Coupled-Cluster Theory: The Extent of non-Hermiticity as a Diagnostic Indicator of Computational Accuracy

The fundamental non-Hermitian nature of the forms of coupled-cluster (CC) theory widely used in quantum chemistry has usually been viewed as a negative, but the present letter shows how this can be used to advantage. Specifically, the non-symmetric nature of the reduced one-particle density matrix (in the molecular orbital basis) is advocated as a diagnostic indicator of computational quality. In the limit of full coupled-cluster theory (which is equivalent to full configuration interaction (FCI)), the electronic wavefunction and correlation energy are exact within a given one-particle basis set and the symmetric character of the exact density matrix is recovered. The extent of the density matrix asymmetry is shown to provide a measure of ``how difficult the problem is'' (like the well-known T$_1$ diagnostic), but its variation with level of theory also gives information about ``how well this particular method works'', irrespective of the difficulty of the problem at hand. The proposed diagnostic is described and applied to a select group of small molecules, and an example of its overall utility for the practicing quantum chemist is illustrated through its application to the beryllium dimer (Be$_2$). Future applications of this idea to excited states, open-shell systems, symmetry-breaking problems and extension of the method to the two-particle density are then proposed.

physics.chem-ph↗