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A density-functional theory including dispersion interactions

The London dispersion interaction is responsible for attraction between non-polar molecules and is of great importance in describing structure and reactivity in many areas of chemistry. Dispersion is difficult to model accurately. Density Functional Theory (DFT) methods, widely used in computational chemistry today, do not include the necessary physics. This often leads to qualitatively incorrect predictions when DFT is applied to dispersion-bound systems. A novel DFT method has been developed which is capable of accurately modeling dispersion. Dispersion attraction between molecules arises when an instantaneous dipole moment in one molecule induces a dipole moment in a second molecule. Our approach proposes that the source of these instantaneous dipole moments is the position-dependent dipole moment of the exchange hole. The model is no more computationally expensive than existing DFTs and gives remarkably accurate dispersion coefficients, intermolecular separations, intermolecular binding energies, and intramolecular conformational energies. Our dispersion theory is also combined with previous post-exact-exchange models of dynamical and nondynamical correlation, yielding a unified exact-exchange-based energy functional called DF07. DF07 overcomes many of the outstanding problems in DFT arising from local exchange approximations. The DF07 model is shown to provide highly accurate results for thermochemistry, kinetics, and van der Waals
interactions. / Thesis (Ph.D, Chemistry) -- Queen's University, 2007-11-29 21:57:09.045

  1. http://hdl.handle.net/1974/926
Identiferoai:union.ndltd.org:LACETR/oai:collectionscanada.gc.ca:OKQ.1974/926
Date04 December 2007
CreatorsJohnson, Erin R.
ContributorsQueen's University (Kingston, Ont.). Theses (Queen's University (Kingston, Ont.))
Source SetsLibrary and Archives Canada ETDs Repository / Centre d'archives des thèses électroniques de Bibliothèque et Archives Canada
LanguageEnglish, English
Detected LanguageEnglish
TypeThesis
Format13177967 bytes, application/pdf
RightsThis publication is made available by the authority of the copyright owner solely for the purpose of private study and research and may not be copied or reproduced except as permitted by the copyright laws without written authority from the copyright owner.
RelationCanadian theses

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