arXiv subjects

Harrison Tuckman

Publications and source records attributed to Harrison Tuckman.

8 recordsLinked to original sources

arXiv2026

Aufbau Suppressed Coupled Cluster Theory for Doubly Excited States

We generalize the Aufbau suppressed coupled cluster formalism into the realm of doubly excited states by deriving, implementing, and testing a wave function initialization strategy that allows the zeroth order wave function to match the largest configurations of a doubly excited reference wave function while maintaining the method's overall asymptotic cost parity with ground state singles and doubles theory. Starting from state-averaged complete active space self consistent field references, this approach produces highly accurate excitation energies for states dominated by a single doubly excited determinant, as well as states in glyoxal and similar molecules where two different doubly excited determinants have large weights. Typical excitation energy errors in both types of states are on the order of 0.15 eV, with the largest observed error being 0.3 eV. These errors stand in stark contrast to equation of motion methods, where typical errors are 4 to 6 eV at the singles and doubles level and 0.4 to 0.8 eV at the full triples level. It remains an open question how best to generalize the Aufbau suppression approach into an even wider variety of multi-configurational double excitations, but these early results offer strong motivation for further investigation.

physics.chem-ph↗

arXiv2025

One-Body Properties and Their Perturbative Accuracy with Aufbau Suppressed Coupled Cluster Theory

We derived and implemented the calculation of the one-body reduced density matrix for Aufbau suppressed coupled cluster theory, from which excited state natural orbitals and one-body properties, like atomic populations and dipole moments, are obtained. We utilized the natural orbitals to refine the ASCC solution for simple valence and Rydberg systems, exploring the process of repeatedly solving the ASCC equations in successive natural orbital bases to achieve independence from the starting molecular orbitals. For dipole moments in small molecules where high-level comparison data is available, we find that the accuracy of ASCC essentially matches that of linear response and equation-of-motion coupled cluster as long as care is taken to preserve the response's perturbative completeness.

physics.chem-ph↗

arXiv2025

Aufbau suppressed coupled cluster as a post-linear-response method

We investigate the ability of Aufbau suppressed coupled cluster theory to act as a post-linear-response correction to widely used linear response methods for electronically excited states. We find that the theory is highly resilient to shortcomings in the underlying linear response method, with final results from less accurate starting points nearly as good as those from the best starting points. This pattern is especially stark in charge transfer states, where the approach converts starting points with multi-eV errors into post-linear-response results with errors on the order of 0.1 eV. These findings highlight the ability of Aufbau suppressed coupled cluster to perform its own orbital relaxations and raise the question of whether initializing it with an orbital relaxed reference is worth the trouble.

physics.chem-ph↗

arXiv2025

Fast and Accurate Charge Transfer Excitations via Nested Aufbau Suppressed Coupled Cluster

Modeling charge transfer well can require treating post-excitation orbital relaxations and handling medium to large molecules in realistic environments. By combining a state-specific correlation treatment with such orbital relaxations, Aufbau suppressed coupled cluster has proven accurate for charge transfer, but, like many coupled cluster methods, it struggles with large system sizes. We derive a low-cost Aufbau suppressed second order perturbation theory and show that, by nesting a small coupled cluster treatment inside of it, computational cost and scaling are reduced while accuracy is maintained. Formal asymptotic costs are dropped from iterative $N^6$ to non-iterative $N^5$ plus iterative $N^3$, and we test an initial implementation that can handle about 100 atoms and 800 orbitals on a single computational node. Charge transfer excitation energy errors are typically below 0.1 eV on average, with an average 0.25 eV improvement over $N^6$-cost equation of motion coupled cluster with singles and doubles.

physics.chem-ph↗

arXiv2025

Improving Aufbau Suppressed Coupled Cluster Through Perturbative Analysis

Guided by perturbative analysis, we improve the accuracy of Aufbau suppressed coupled cluster theory in simple single excitations, multi-configurational single excitations, and charge transfer excitations while keeping the cost of its leading-order terms precisely in line with ground state coupled cluster. Combining these accuracy improvements with a more efficient implementation based on spin-adaptation, we observe high accuracy in a large test set of single excitations, and, in particular, a mean unsigned error for charge transfer states that outperforms equation-of-motion coupled cluster theory by 0.25 eV. We discuss how these results are achieved via a systematic identification of which amplitudes to prioritize for single- and multi-configurational excited states, and how this prioritization differs in important ways from the ground state theory. In particular, our data show that a partial linearization of the theory increases accuracy by mitigating unwanted side effects of Aufbau suppression.

physics.chem-ph↗

arXiv2023

Aufbau Suppressed Coupled Cluster Theory for Electronically Excited States

We introduce an approach to improve single-reference coupled cluster theory in settings where the Aufbau determinant is absent from or plays only a small role in the true wave function. Using a de-excitation operator that can be efficiently hidden within a similarity transform, we create a coupled cluster wave function in which de-excitations work to suppress the Aufbau determinant and produce wave functions dominated by other determinants. Thanks to an invertible and fully exponential form, the approach is systematically improvable, size consistent, size extensive, and, interestingly, size intensive in a granular way that should make the adoption of some ground state techniques such as local correlation relatively straightforward. In this initial study, we apply the general formalism to create a state-specific method for orbital-relaxed singly excited states. We find that this approach matches the accuracy of similar-cost equation-of-motion methods in valence excitations while offering improved accuracy for charge transfer states. We also find the approach to be more accurate than excited-state-specific perturbation theory in both types of states.

physics.chem-ph↗

arXiv2023

Studying excited-state-specific perturbation theory on the Thiel set

We explore the performance of a recently-introduced $N^5$-scaling excited-state-specific second order perturbation theory (ESMP2) on the singlet excitations of the Thiel benchmarking set. We find that, without regularization, ESMP2 is quite sensitive to $\pi$ system size, performing well in molecules with small $\pi$ systems but poorly in those with larger $\pi$ systems. With regularization, ESMP2 is far less sensitive to $\pi$ system size and shows a higher overall accuracy on the Thiel set than CC2, EOM-CCSD, CC3, and a wide variety of time-dependent density functional approaches. Unsurprisingly, even regularized ESMP2 is less accurate than multi-reference perturbation theory on this test set, which can in part be explained by the set's inclusion of some doubly excited states but none of the strong charge transfer states that often pose challenges for state-averaging. Beyond energetics, we find that the ESMP2 doubles norm offers a relatively low-cost way to test for doubly excited character without the need to define an active space.

physics.chem-ph↗

arXiv2023

An Excited-State-Specific Pseudoprojected Coupled-Cluster Theory

We present an excited-state-specific coupled-cluster approach in which both the molecular orbitals and cluster amplitudes are optimized for an individual excited state. The theory is formulated via a pseudoprojection of the traditional coupled-cluster wavefunction that allows correlation effects to be introduced atop an excited state mean field starting point. The approach shares much in common with ground state CCSD, including size extensivity and an $N^6$ cost scaling. Preliminary numerical tests show that, when augmented with $N^5$-cost perturbative corrections for key terms, the method can improve over excited-state-specific second order perturbation theory in valence, charge transfer, and Rydberg states.

physics.chem-ph↗