(10-0928) Prof. John Reynolds, University of Florida

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Event Details
  • Date/Time:
    • Tuesday September 28, 2010 - Wednesday September 29, 2010
      4:00 pm - 4:59 pm
  • Location: MoSE G011
  • Phone:
  • URL:
  • Email:
  • Fee(s):
    N/A
  • Extras:
Contact
Shirley Tomes
Chemistry & Biochemistry
Contact Shirley Tomes
404-894-0591
Summaries

Summary Sentence: Prof. John Reynolds, University of Florida

Full Summary: Prof. John Reynolds, University of Florida Π-Conjugated Polymers: Pushing the Limits Using Chemistry Special Seminar

Prof. John Reynolds, University of Florida

Π-Conjugated Polymers: Pushing the Limits Using Chemistry

Special Seminar

Conjugated polymers provide a unique encompassing set of structurally tunable optical, electronic transport, and redox properties that allows their present and potential use in a host of applications which span nearly metallic materials, field effect transistors, light emitting diodes, solar cells and photodetectors, chem/bio-sensors, electrochromism, along with batteries and supercapacitors. Each of these properties can be controlled by repeat unit, macromolecular, and solid-state structure which are all dependent on the chemical identity of each system. In this presentation, we will explore how chemistry enables the creation of new polymers where a specific property is pushed towards its limit. Dioxypyrrole-based polymers provide the most electron rich, and most easily oxidized, conjugated polymer family as desired for stable conductivity and long lived redox switching.1 The flexible synthetic chemistry of dioxythiophene-based polymers has allowed us to complete the color palette of vibrantly colored to transmissive switching electrochromes of any color, including black.2,3 Two band absorption induced by the incorporation of a donor-acceptor-donor triad in the polymer chain induces long wavelength light collection well into the near infrared for photovoltaic devices,4 and even into the mid infrared as desired for photodetectors.5 Accessing highly solution processble conjugated polymers allows us to spray- and print-process for a response or interaction over large-areas and on flexible substrates. These examples serve to demonstrate the approach the chemist uses in conjugated polymer research, and provides insight for making great strides in the future.

1Walczak, R. M.; Reynolds, J. R. Adv. Mater. 2006, 18, 1121-1131. “Poly(3,4-alkylenedioxypyrroles): The PXDOPs as Versatile yet Underutilized Electro-active and Conducting Polymers”
2Beaujuge, P.M.; Reynolds, J.R. Chem. Reviews, Special Edition â€" Organic Electronics 2010, 110, 268-320. “Color Control in Π-Conjugated Organic Polymers for Use in Electrochromic Devices”
3Beaujuge, P.; Ellinger, S.; Reynolds, J.R. Nature Materials, 2008, 7, 795-799. “The Donor-Acceptor Approach Allows a Black to Transmissive Switching Polymer Electrochrome”
4Beaujuge, P.M.; Amb, C.M.; Reynolds, J.R. Acc. Chem. Res., ASAP August 20, 2010 DOI: 10.1021/ar100043u “Spectral Engineering in Π-Conjugated Polymers with Intramolecular Donor-Acceptor Interactions”
5Steckler, T.T., Zhang, X., Hwang, J., Honeyager, R., Ohira, S., Zhang, X-H., Grant, A., Ellinger, S., Odom, S.A., Seat, D., Tanner, D.B., Rinzler, A.G., Barlow, S., Bredas, J-L., Kippelen, B., Marder, S.R., Reynolds, J.R. J. Am. Chem. Soc. 2009,131, 2824-2826. “A Spray Processable, Low Bandgap, and Ambipolar Donor-Acceptor Conjugated Polymer”

For more information contact Prof. Seth Marder (404-385-5-6048).

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Additional Information

In Campus Calendar
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School of Chemistry and Biochemistry

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Categories
Seminar/Lecture/Colloquium
Keywords
physical chemistry
Status
  • Created By: Shirley Tomes
  • Workflow Status: Published
  • Created On: Sep 14, 2010 - 8:00pm
  • Last Updated: Oct 7, 2016 - 9:47pm