Award Date
5-1-2016
Degree Type
Thesis
Degree Name
Master of Science (MS)
Department
Chemistry and Biochemistry
First Committee Member
Dong-Chan Lee
Second Committee Member
Gary Kleiger
Third Committee Member
Kathleen Robins
Fourth Committee Member
Woosoon Yim
Number of Pages
82
Abstract
Development of electron-accepting (n-type) semiconductors used in organic photovoltaic cells and field effect transistors has been an area of research with less advancement compared to their electron-donating (p-type) counterparts. Currently, the highest performing n-type semiconductor is a fullerene-based derivative (PCBM) with a favorable ELUMO of -4.08 eV. However, PCBM has limited absorption in the visible region and fixed electron affinity. This work focuses on the development of self-assembling n-type materials with controllable electronic properties by strategically lowering ELUMO to a level comparable to PCBM. Molecular design follows an acceptor-acceptor'-acceptor (A-A'-A) configuration; with A being two 2,3-dioctyloxyphenazine substituents connected to A’ with a C-C triple bond. A’ was altered to increase the electron deficiency using benzothiadiazole (BTD), naphthalene diimide (NDI), and perylene-tetracarboxylic diimide (PTCDI). Based on this molecular design, four new n-type materials (BTD-P, NDI-P-1, NDI-P-2, PTCDI-P) were successfully synthesized with low ELUMO values of -3.34 eV, -3.90 eV, -3.90, and -3.97 eV, respectively. Photophysical, thermal, and electrochemical properties were studied using UV-Visible absorption and fluorescence emission spectroscopy, differential scanning calorimetry, thermogravimetric analysis, and cyclic voltammetry. Theoretical evaluations were conducted to understand the experimental electronic properties. Charge-transfer (CT) was also used to test the accepting properties of the title molecules when paired with a pyrene donor. Successful CT results were seen using NDI-P-1, which were confirmed through UV-Vis and fluorescence spectroscopy. The morphology of the CT complex was studied with polarized optical microscopy (POM). Additionally, fluorescence resonance energy transfer (FRET) through organogelation was studied with BTD-P as a donor with NDI-P-2 as an acceptor. It was found that FRET was efficient even at low acceptor concentration of 5mole%. FRET results were characterized with fluorescence spectroscopy and POM.
Keywords
Molecular Design; Organic Chemistry; Semiconductors
Disciplines
Chemistry
File Format
Degree Grantor
University of Nevada, Las Vegas
Language
English
Repository Citation
Zaugg, Kelly Nicole, "Strategic Molecular Design to Engineer the Electron Affinity of Self-Assembling Organic Semiconductors" (2016). UNLV Theses, Dissertations, Professional Papers, and Capstones. 2767.
http://dx.doi.org/10.34917/9112217
Rights
IN COPYRIGHT. For more information about this rights statement, please visit http://rightsstatements.org/vocab/InC/1.0/