Date of Award
Spring 5-2017
Degree Type
Honors College Thesis
Department
Chemistry and Biochemistry
First Advisor
Song Guo
Advisor Department
Chemistry and Biochemistry
Abstract
Although organic electronic materials are flexible, cheap to fabricate, and molecularly tunable, their performance has generally been less efficient than that of their inorganic counterparts. Chemical doping has been attempted as a method to increase the efficiency of organic materials. During this process, an organic material, typically a conjugated polymer, is exposed to an oxidant/reductant, called a dopant. Electron transfer between host polymer and dopant molecules increases the charge carrier density in the doped host material, making it a more efficient conductor. The effects of doping using 2,3,5,6-tetrafluoro-tetracyanoquinodimethane (F4TCNQ) on low molecular weight poly(3-hexylthiophene-2,5-diyl) (LMW P3HT) in varying ratios of a decane/toluene solvent was investigated. Increasing the fraction of decane, a nonpolar bad solvent that does not facilitate charge transfer, forces the P3HT to aggregate very quickly. A comparison is made between the UV-vis spectra of samples prepared with decane and those of samples prepared in pure toluene. By comparing the chemical doping behavior between aggregated and non-aggregated forms of P3HT, the influences of P3HT aggregation on their chemical doping kinetics are elucidated. The experimental results obtained support the hypothesis that P3HT must undergo its aggregation step before a doping product can be formed.
Copyright
Copyright for this thesis is owned by the author. It may be freely accessed by all users. However, any reuse or reproduction not covered by the exceptions of the Fair Use or Educational Use clauses of U.S. Copyright Law or without permission of the copyright holder may be a violation of federal law. Contact the administrator if you have additional questions.
Recommended Citation
Travis, Skye R., "Kinetic Study of Conjugated Polymer Packing and Agglomeration" (2017). Honors Theses. 480.
https://aquila.usm.edu/honors_theses/480