Toward the Systematic Design of Complex Materials from Structural Motifs
General Material Designation
[Thesis]
First Statement of Responsibility
SMIDT, TESS Eleonora
Subsequent Statement of Responsibility
Neaton, Jeffrey B
.PUBLICATION, DISTRIBUTION, ETC
Date of Publication, Distribution, etc.
2018
DISSERTATION (THESIS) NOTE
Body granting the degree
Neaton, Jeffrey B
Text preceding or following the note
2018
SUMMARY OR ABSTRACT
Text of Note
With first-principles calculations based on density functional theory, we can predict with good accuracy the electronic ground state properties of a fixed arrangement of nuclei in a molecule or crystal. However, the potential of this formalism and approach is not fully utilized; most calculations are performed on experimentally determined structures and stoichiometric substitutions of those systems. This in part stems from the difficulty of systematically generating 3D geometries that are chemically valid under the complex interactions existing in materials. Designing materials is a bottleneck for computational materials exploration; there is a need for systematic design tools that can keep up with our calculation capacity. Identifying a higher level language to articulate designs at the atomic scale rather than simply points in 3D space can aid in developing these tools. Constituent atoms of materials tend to arrange in recognizable patterns with defined symmetry such as coordination polyhedra in transition metal oxides or subgroups of organic molecules; we call these structural motifs. In this thesis, we advance a variety of systematic strategies for understanding complex materials from structural motifs on the atomic scale with an eye towards future design. In collaboration with experiment, we introduce the harmonic honeycomb iridates with frustrated, spin-anisotropic magnetism. At the atomic level, the harmonic honeycomb iridates have identical local geometry where each iridium atom octahedrally coordinated by oxygen hosts a