All-Conjugated Block Copolymers for Organic Photovoltaic Applications

dc.contributor.advisorVerduzco, Rafaelen_US
dc.contributor.committeeMemberChapman, Walter Gen_US
dc.contributor.committeeMemberHartgerink, Jeffrey Den_US
dc.creatorSmith, Kendall Allenen_US
dc.date.accessioned2016-01-27T17:14:35Zen_US
dc.date.available2016-01-27T17:14:35Zen_US
dc.date.created2014-12en_US
dc.date.issued2014-12-03en_US
dc.date.submittedDecember 2014en_US
dc.date.updated2016-01-27T17:14:35Zen_US
dc.descriptionInfo on supplemental videos starting on page 171.en_US
dc.description.abstractConventional inorganic solar technologies are expensive due to the high cost of processing, while organic materials have significant cost advantages in the raw materials and ease of processing. Unfortunately, organic devices suffer from low efficiency due to difficulty in transporting charges to the electrodes. Typical devices mix the donor and acceptor components and anneal them to allow for phase separation. However, because the phase separation is uncontrolled, domains may be larger than optimal and isolated domains can be formed reducing efficiency. All-conjugated block copolymers have the potential to improve efficiency by creating an ordered structure with controlled domains and continuous pathways through self-assembly. In this work, the relationships between structure, optoelectronic properties, and processing conditions for these materials are systematically investigated using two routes to obtain the materials. In one route, functionalized catalysts are used to initiate controlled polymerizations of two different polymers. These well functionalized precursors are then joined together using copper catalyzed azide alkyne click chemistry. In a second route, a sequential polymerization route is employed where one polymer is synthesized with a well-defined end-group. The polymer is then used as a macroreagent to end-cap a Suzuki polycondensation reaction, yielding materials with direct conjugation between the blocks. The first route yields well-defined materials, whereas the second can access a broader variety of polymers. For all these materials, processing conditions are varied and the morphology of the all-conjugated block copolymers are analyzed by a combination of grazing-incidence X-ray scattering, neutron scattering and reflectivity, atomic force microscopy, and transmission electron microscopy. Materials are found to self-assemble into thermodynamically stable structures with well-defined length scales. It is found that crystallization of either block is predominant in all block copolymers studied, but at intermediate ratios crystallization of both blocks is observed. Processing conditions such as casting temperature, annealing duration, and speed of quenching to room temperature are found to have important effects on thin film crystallinity and orientation of the π-π stacking direction of polymer crystallites. By varying the annealing duration and quenching speed, crystallization of either or both block can be obtained.en_US
dc.format.mimetypeapplication/pdfen_US
dc.identifier.citationSmith, Kendall Allen. "All-Conjugated Block Copolymers for Organic Photovoltaic Applications." (2014) Diss., Rice University. <a href="https://hdl.handle.net/1911/88154">https://hdl.handle.net/1911/88154</a>.en_US
dc.identifier.urihttps://hdl.handle.net/1911/88154en_US
dc.language.isoengen_US
dc.rightsCopyright is held by the author, unless otherwise indicated. Permission to reuse, publish, or reproduce the work beyond the bounds of fair use or other exemptions to copyright law must be obtained from the copyright holder.en_US
dc.subjectblock copolymersen_US
dc.subjectP3HTen_US
dc.subjectpoly(3-hexylthiophene)en_US
dc.subjectP3DDTen_US
dc.subjectpoly(3-dodecylthiophene)en_US
dc.subjectself-assemblyen_US
dc.subjectcrystallizationen_US
dc.subjectorganic photovoltaicsen_US
dc.subjectorganic solar cells.en_US
dc.titleAll-Conjugated Block Copolymers for Organic Photovoltaic Applicationsen_US
dc.typeThesisen_US
dc.type.dcmiMovingImageen_US
dc.type.materialTexten_US
thesis.degree.departmentChemical and Biomolecular Engineeringen_US
thesis.degree.disciplineEngineeringen_US
thesis.degree.grantorRice Universityen_US
thesis.degree.levelDoctoralen_US
thesis.degree.nameDoctor of Philosophyen_US
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