Title:
The Role of Non-covalent Interactions in Band-gap Tuning, Conformation and Self-assembly

dc.contributor.author Skabara, Peter J. en_US
dc.contributor.corporatename University of Strathclyde. Dept. of Pure and Applied Chemistry en_US
dc.contributor.corporatename Georgia Institute of Technology. School of Electrical and Computer Engineering en_US
dc.contributor.corporatename Georgia Institute of Technology. School of Chemical and Biomolecular Engineering en_US
dc.contributor.corporatename Georgia Institute of Technology. School of Materials Science and Engineering en_US
dc.contributor.corporatename Georgia Institute of Technology. School of Mechanical Engineering en_US
dc.contributor.corporatename Georgia Institute of Technology. School of Chemistry and Biochemistry en_US
dc.contributor.corporatename Georgia Institute of Technology. Center for Organic Photonics and Electronics en_US
dc.date.accessioned 2013-08-16T18:43:34Z
dc.date.available 2013-08-16T18:43:34Z
dc.date.issued 2013-08-06
dc.description Peter J. Skabara, Professor at the Department of Pure and Applied Chemistry at the University of Strathclyde (Glasgow, UK) presented a lecture on August 6, 2013, from 11:00 am to 12:00 pm, in the Molecular Science and Engineering Building, room 1201A. en_US
dc.description Runtime: 48:39 minutes. en_US
dc.description.abstract The extent to which the optoelectronic properties of molecules are controlled by their conformation and packing is now well appreciated. In particular, the planarity (or nonplanarity) of a molecule has a dramatic influence on its behavior, and hence on its potential application. In the context of light emission, disorder can be beneficial in controlling aggregation, but for photovoltaics and transistors where low energy absorption and effective charge transport are key issues, planar molecules are preferable. Of particular relevance to this talk is the development of planarised conjugated architectures that should support much-enhanced charge transport properties as a result of their ability to self-assemble into tightly packed frameworks. For example, compound 1 (m = 10 ⁻² cm² V⁻¹ s ⁻¹) orders into a 3-dimensional network of close contacts both in crystalline form and as a thin film. This high level of self-assembly is achieved through p-p stacking in 2D and non-covalent interactions between the S and N atoms of adjacent molecules in the third. The nature of these interactions is not entirely clear, but one possible source of an attractive potential is a 3c-2e interaction between lone pairs and relatively low-lying antibonding orbitals, although these are likely to be counteracted to some extent by significant lone pair-lone pair repulsions. The 3D nature of the material represents a unique motif for highly efficient charge transport. A second example, polymer 2 (m = 10 ⁻³ cm² V⁻¹ s ⁻¹), has a planar repeat unit in the solid state as a result of close intramolecular sulfur/fluorine and hydrogen/fluorine contacts. Interestingly, variations in the absorption spectrum of these molecules suggest that the band gap is very sensitive to the degree of planarity. Whilst the mobility values for 1 and 2 are modest, the importance of the work is that it establishes a principle for the rational design of second generation materials with enhanced charge-transport properties. This lecture will discuss several further examples that underline the importance and influence of non-covalent interaction in organic semiconductors. en_US
dc.description.advisor en_US
dc.format.extent 48:39 minutes
dc.identifier.uri http://hdl.handle.net/1853/48708
dc.language.iso en_US en_US
dc.publisher Georgia Institute of Technology en_US
dc.relation.ispartofseries COPE Seminar Series en_US
dc.subject Organic semiconductors en_US
dc.subject Band gap tuning en_US
dc.subject Heteroatom en_US
dc.subject Interactions en_US
dc.title The Role of Non-covalent Interactions in Band-gap Tuning, Conformation and Self-assembly en_US
dc.type Moving Image
dc.type.genre Lecture
dspace.entity.type Publication
local.contributor.corporatename Center for Organic Photonics and Electronics
local.relation.ispartofseries COPE Seminar Series
relation.isOrgUnitOfPublication 43f8dc5f-0678-4f07-b44a-edbf587c338f
relation.isSeriesOfPublication 642bd61c-9b87-4309-a7dd-1d073b437365
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