The Role of Disorder in the Charge Dissociation and Recombination Processes of Organic Photovoltaic Materials

Simple item page
dc.contributor.advisorBittner, Eric R.
dc.contributor.committeeMemberLubchenko, Vassiliy
dc.contributor.committeeMemberSu, Wu-Pei
dc.contributor.committeeMemberSmith, Mark
dc.contributor.committeeMemberBrgoch, Jakoah
dc.creatorLankevich, Vladimir 1991-
dc.date.accessioned2019-05-23T13:12:47Z
dc.date.createdAugust 2018
dc.date.issued2018-08
dc.date.submittedAugust 2018
dc.date.updated2019-05-23T13:12:48Z
dc.description.abstractOrganic Photovoltaic devices (OPVs) are becoming adequately cost and energy efficient to be considered a good investment and it is, therefore, especially important to have a concrete understanding of their operation. In this work, we use a fully quantum mechanical model of the electronic states of a bulk-heterojunction interface to investigate how presence of disorder in OPVs affects the recombination of triplet charge-transfer states and influences the free energy of an electron as it separates away from the interface into the free carrier phase. Our model simplifies complicated molecular structures to a lattice system, while taking into account electron and hole Coulombic and exchange interactions, lattice vibrations, and electron-phonon couplings. In addition, we examine the role of band-width and interfacial driving forces in determining the dissociation free energy of an electron/hole pair. With proper statistical treatment of the CT energies we recover experimentally observed ''hot'' and "cold'' exciton dissociation pathways. We also recover experimental values for the open-circuit voltage for the systems with 50-100 meV of energy disorder. Our model combines quantum and statistical treatments of a system with the large number of parameters and all possible electron-hole configurations to give results that provide a unifying picture linking various proposed mechanisms for charge separation. With many different theoretical tools and protocols available, our model stands out as combines scalability of molecular dynamics simulations with quantum mechanical treatment of electronics states.
dc.description.departmentChemistry, Department of
dc.format.digitalOriginborn digital
dc.format.mimetypeapplication/pdf
dc.identifier.urihttps://hdl.handle.net/10657/3958
dc.language.isoeng
dc.rightsThe author of this work is the copyright owner. UH Libraries and the Texas Digital Library have their permission to store and provide access to this work. Further transmission, reproduction, or presentation of this work is prohibited except with permission of the author(s).
dc.subjectOrganic photovoltaics
dc.subjectExciton
dc.subjectDisorder
dc.subjectLattice Model
dc.subjectEntropy
dc.titleThe Role of Disorder in the Charge Dissociation and Recombination Processes of Organic Photovoltaic Materials
dc.type.dcmiText
dc.type.genreThesis
local.embargo.lift2020-08-01
local.embargo.terms2020-08-01
thesis.degree.collegeCollege of Natural Sciences and Mathematics
thesis.degree.departmentChemistry, Department of
thesis.degree.disciplineChemistry
thesis.degree.grantorUniversity of Houston
thesis.degree.levelDoctoral
thesis.degree.nameDoctor of Philosophy

Files

Original bundle

Now showing 1 - 1 of 1
No Thumbnail Available
Name:
LANKEVICH-DISSERTATION-2018.pdf
Size:
7.86 MB
Format:
Adobe Portable Document Format
Download

License bundle

Now showing 1 - 2 of 2
No Thumbnail Available
Name:
PROQUEST_LICENSE.txt
Size:
4.43 KB
Format:
Plain Text
Description:
Download
No Thumbnail Available
Name:
LICENSE.txt
Size:
1.82 KB
Format:
Plain Text
Description:
Download

Collections

Published ETD Collection