Organic electronics are becoming an increasingly important part of the semiconductor industry, with myriad applications enabled by their low cost, solution processability, and electrical conductivity. Charge transport in electronic applications involving organic semiconductor materials depends strongly on the electronic properties of nanoscale interfaces. Local variations in molecular environments can have a significant impact on the interfacial electronic properties, and subsequently the organic semiconductor electronic structure. Here, we use scanning tunneling microscopy and spectroscopy, supported by theoretical calculations, to investigate the impact of the local adsorption environment on the local density of states of oligothiophenes, carbon nanohoops, and carbon nanotubes. First, we present work showing that, for alkyl-substituted quaterthiophenes, molecular packing and electronic structure at interfaces differ substantially from the bulk, and a significant degree of structural and electronic variation occurs even in this relatively simple system. Then, we report on investigations of longer alkyl-substituted oligothiophenes, were we found a variety of planar molecular conformations that surprising exhibited similar, particle-in-a-box-like progressions of unoccupied molecular orbitals. Next, we share our research that found, for the first time, metal surface electrons confined within single adsorbed molecules. Finally, we study the impact of electrostatic defects in both metal and dielectric substrates on single-walled carbon nanotubes. The research presented in this dissertation increases our understanding of organic semiconductor interfaces and the impact of said interfaces on local molecular electronic structure, thereby aiding future organic semiconductor technological development. / 10000-01-01
Identifer | oai:union.ndltd.org:uoregon.edu/oai:scholarsbank.uoregon.edu:1794/23711 |
Date | 06 September 2018 |
Creators | Taber, Benjamen |
Contributors | Guenza, Marina |
Publisher | University of Oregon |
Source Sets | University of Oregon |
Language | en_US |
Detected Language | English |
Type | Electronic Thesis or Dissertation |
Rights | All Rights Reserved. |
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