

@mastersthesis {6906,
	title = {Theory and {Applications} of {Quantum} {Monte} {Carlo}},
	year = {2015},
	note = {3735264},
	school = {University of Pittsburgh},
	type = {phdPh.{D}.},
	address = {Ann Arbor},
	abstract = {With the development of peta-scale computers and exa-scale only a few years away, the quantum Monte Carlo (QMC) method, with favorable scaling and inherent parrallelizability, is poised to increase its impact on the electronic structure community. The most widely used variation of QMC is the diffusion Monte Carlo (DMC) method. The accuracy of the DMC method is only limited by the trial wave function that it employs. The effect of the trial wave function is studied here by initially developing correlation-consistent Gaussian basis sets for use in DMC calculations. These basis sets give a low variance in variance Monte Carlo calculations and improved convergence in DMC. The orbital type used in the trial wave function is then investigated, and it is shown that Brueckner orbitals result in a DMC energy comparable to a DMC energy with orbitals from density functional theory and significantly lower than orbitals from Hartree-Fock theory. Three large weakly interacting systems are then studied; a water-16 isomer, a methane clathrate, and a carbon dioxide clathrate. The DMC method is seen to be in good agreement with MP2 calculations and provides reliable benchmarks. Several strongly correlated systems are then studied. An H 4 model system that allows for a fine tuning of the multi-configurational character of the wave function shows when the accuracy of the DMC method with a single Slater-determinant trial function begins to deviate from multi-reference benchmarks. The weakly interacting face-to-face ethylene dimer is studied with and without a rotation around the π bond, which is used to increase the multi-configurational nature of the wave function. This test shows that the effect of a multi-configurational wave function in weakly interacting systems causes DMC with a single Slater-determinant to be unable to achieve sub-chemical accuracy. The beryllium dimer is studied, and it is shown that a very large determinant expansion is required for DMC to predict a binding energy that is in close agreement with experiment. Finally, water interacting with increasingly large acenes is studied, as is the benzene and anthracene dimer. Deviations from benchmarks are discussed.},
	keywords = {0494:Physical chemistry, 0599:Quantum physics, 0753:Theoretical physics, Diffusion Monte Carlo method, Electronic structure community, Physical Chemistry, Pure sciences, Quantum Monte Carlo, Quantum physics, Theoretical physics},
	url = {http://search.proquest.com/docview/1749026534?accountid=14270},
	author = {Deible, Michael John}
}
