The Efficient Computation of Field-Dependent Molecular Properties in the Frequency and Time Domains
| dc.contributor.author | Peyton, Benjamin Gilbert | en |
| dc.contributor.committeechair | Crawford, Daniel | en |
| dc.contributor.committeemember | Troya, Diego | en |
| dc.contributor.committeemember | Morris, John R. | en |
| dc.contributor.committeemember | Mayhall, Nicholas | en |
| dc.contributor.department | Chemistry | en |
| dc.date.accessioned | 2022-06-01T08:00:33Z | en |
| dc.date.available | 2022-06-01T08:00:33Z | en |
| dc.date.issued | 2022-05-31 | en |
| dc.description.abstract | The efficient computation of dynamic (time-dependent) molecular properties is a broad field with numerous applications in aiding molecular synthesis and design, with a particular preva- lence in spectroscopic predictions. Typical methods for computing the response of a molecu- lar system to an electromagnetic field (EMF) considers a quantum mechanical description of the molecule and a classical approximation for the EMF. Methods for describing light-matter interactions with high-accuracy electronic structure methods, such as coupled cluster (CC), are discussed, with a focus on improving the efficiency of such methods. The CC method suffers from high-degree polynomial scaling. In addition to the ground-state calculation, computing dynamic properties requires the description of sensitive excited-state effects. The cost of such methods often prohibits the accurate calculation of response prop- erties for systems of significant importance, such as large-molecule drug candidates or chiral species present in biological systems. While the literature is ripe with reduced-scaling meth- ods for CC ground-state calculations, considerably fewer approaches have been applied to excited-state properties, with even fewer still providing adequate results for realistic systems. This work presents three studies on the reduction of the cost of molecular property evalu- ations, in the hopes of closing this gap in the literature and widening the scope of current theoretical methods. There are two main ways of simulating time-dependent light-matter interactions: one may consider these effects in the frequency domain, where the response of the system to an EMF is computed directly; or, the response may be considered explicitly in the time domain, where wave function (or density) parameters can be propagated in time and examined in detail. Each methodology has unique advantages and computational bottlenecks. The first two studies focus on frequency-domain calculations, and employ fragmentation and machine- learning techniques to reduce the cost of single-molecule calculations or sets of calculations across a series of geometric conformations. The third study presents a novel application of the local correlation technique to real-time CC calculations, and highlights deficiencies and possible solutions to the approach. | en |
| dc.description.abstractgeneral | Theoretical chemistry plays a key role in connecting experimental results with physical inter- pretation. Paramount to the success of theoretical methods is the ability to predict molecular properties without the need for costly high-throughput synthesis, aiding in the determina- tion of molecular structure and the design of new materials. Light-matter interactions, which govern spectroscopic techniques, are particularly complicated, and sensitive to the theoreti- cal tools employed in their prediction. Compounding the issue of accuracy is one of efficiency — accurate theoretical methods typically incur steep scaling of computational cost (memory and processor time) with respect to the size of the system. An important aspect in improving the efficiency of these methods is understanding the nature of light-matter interactions at a quantum level. Many unanswered questions still remain, such as, "Can light-matter interactions be thought of as a sum of interactions be- tween smaller fragments of the system?" and "Can conventional methods of accelerating ground-state calculations be expected to perform well for spectroscopic properties?" The present work seeks to answer these questions through three studies, focusing on improving the efficiency of these techniques, while simultaneously addressing their fundamental flaws and providing reasonable alternatives. | en |
| dc.description.degree | Doctor of Philosophy | en |
| dc.format.medium | ETD | en |
| dc.identifier.other | vt_gsexam:35108 | en |
| dc.identifier.uri | http://hdl.handle.net/10919/110375 | en |
| dc.language.iso | en | en |
| dc.publisher | Virginia Tech | en |
| dc.rights | Creative Commons Attribution-ShareAlike 4.0 International | en |
| dc.rights.uri | http://creativecommons.org/licenses/by-sa/4.0/ | en |
| dc.subject | Electronic structure theory | en |
| dc.subject | machine learning | en |
| dc.subject | coupled cluster | en |
| dc.subject | local correlation | en |
| dc.title | The Efficient Computation of Field-Dependent Molecular Properties in the Frequency and Time Domains | en |
| dc.type | Dissertation | en |
| thesis.degree.discipline | Chemistry | en |
| thesis.degree.grantor | Virginia Polytechnic Institute and State University | en |
| thesis.degree.level | doctoral | en |
| thesis.degree.name | Doctor of Philosophy | en |