First-principles study of nanostructured materials: wires, interfaces, and bulk systems

Due to recent advances in computational hardware and code accessibility, state-of-the-art calculations are currently employed to investigate materials at the nanoscale with varying levels of accuracy. As such, this dissertation highlights a series of materials ranging from one-dimensional wires, to reactive surfaces, to bulk crystals. Initial characterizations for all considered materials are carried out using density functional theory where additional approximations are utilized to obtain more complex quantities. For Millon's salt, first-principles calculations confirm a quasi-one-dimensional description where the metallic backbone influences electronic properties while hydrogen-bonding between ligands results in structural stability. We show that valence band dispersion can be controlled via strain or ligand substitution, pointing to tunable hole-carrier possibilities. Optical properties are also addressed with respect to experimental and theoretical findings. Our focus then shifts to titanium dioxide, a popular and promising photocatalyst. Specific nitrogen doping on the anatase (001) surface introduces intra gap states accessible for photoactivation in the visible. The additional presence of a fluorine dopant or oxygen vacancy enhances the density of these particular states available for transitions. Titanium dioxide also has experimentally displayed involvement in carbon dioxide reduction mechanisms. From first-principles calculations, anatase (001) surfaces containing an oxygen vacancy exhibit an increased potential for carbon dioxide to undergo reduction due to an exposed titanium atom in comparison to the pristine case. Other binding configurations on both types of surfaces suggest the existence of alternative conversion pathways. As a recently realized plasmonic material, titanium nitride proves advantageous in relation to more traditional materials, e.g., gold or silver; one of the main factors stems from its tunable permittivity. We investigate this aspect by theoretically incorporating defects into titanium nitride, which introduces a systematic approach to control plasmonic activity over a broad frequency range. Finally, lifetimes of hot-electrons, originating from plasmonic decay, for instance, possess finite lifetimes in titanium nitride, as well as in other similar materials, that are described by electron-electron interactions through the electron self-energy. Average lifetimes resemble those obtained with a free electron gas model while details of the band structure influence lifetime behavior. Calculations exploring factors affecting these lifetimes are presented