Use this URL to cite or link to this record in EThOS: https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.769448
Title: Development of one-step post-polymerisation methods for semiconducting polymers
Author: Creamer, Adam David
ISNI:       0000 0004 7657 7383
Awarding Body: Imperial College London
Current Institution: Imperial College London
Date of Award: 2018
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Abstract:
Organic semiconductors have several advantages over their inorganic counterparts. For example, the solution processability allows for the fabrication of flexible, lightweight and low-cost semiconducting devices. However, much work is needed to compete with the high-performance of inorganics. The first half of this work focuses primarily on nucleophilic aromatic substitution (SNAr) reactions with molecules and polymers containing the fluorinated 2,1,3-benzothiadiazole (BT) unit. Chapter 2 explores the effect the type of heteroatom on the BT unit (N, O and S) of a carbazole-based polymer has on the optical properties and organic photovoltaic (OPV) performance. The following chapter focuses on post-polymerisation SNAr reactions, in which thiols were found to displace fluorine groups on a variety of polymers, including polymers containing fluorinated benzotriazole (BTz) and thienothiophene (TT) units instead of BT. The reaction was then taken a step further, by substituting fluorine atoms on P(F8fBT) with a diverse range of end-functionalised thiols, thioacetates and alcohols. It was also found that the amount of thiol substitution could be finely tuned, which led to the development of multifunctionalised polymers. The second half of this thesis explores the possible applications of the BT SNAr reaction towards semiconducting polymer nanoparticles (SPN) and OPVs. In Chapter 4, SPNs from polymers functionalised with azide and carboxylic groups were synthesised and the surface was found to be reactive to strained-alkynes and amines, respectively. In the final chapter, a trimethoxysilane-functionalised OPV polymer was synthesised and was found to increase the thermal stability of devices via cross-linking, with no additives required.
Supervisor: Heeney, Martin Sponsor: Commonwealth Scientific and Industrial Research Organization (Australia)
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.769448  DOI:
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