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JOURNAL ARTICLE

Coherent Exciton Delocalization in a Two-State DNA-Templated Dye Aggregate System

Brittany L Cannon, Donald L Kellis, Lance K Patten, Paul H Davis, Jeunghoon Lee, Elton Graugnard, Bernard Yurke, William B Knowlton
Journal of Physical Chemistry. A 2017 September 21, 121 (37): 6905-6916
28813152
Coherent exciton delocalization in dye aggregate systems gives rise to a variety of intriguing optical phenomena, including J- and H-aggregate behavior and Davydov splitting. Systems that exhibit coherent exciton delocalization at room temperature are of interest for the development of artificial light-harvesting devices, colorimetric detection schemes, and quantum computers. Here, we report on a simple dye system templated by DNA that exhibits tunable optical properties. At low salt and DNA concentrations, a DNA duplex with two internally functionalized Cy5 dyes (i.e., dimer) persists and displays predominantly J-aggregate behavior. Increasing the salt and/or DNA concentrations was found to promote coupling between two of the DNA duplexes via branch migration, thus forming a four-armed junction (i.e., tetramer) with H-aggregate behavior. This H-tetramer aggregate exhibits a surprisingly large Davydov splitting in its absorbance spectrum that produces a visible color change of the solution from cyan to violet and gives clear evidence of coherent exciton delocalization.

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