In situ measurements of the optical absorption of dioxythiophene-based conjugated polymers
Name
Hwang-2011-In situ measurements of the optical absorption.pdf
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1.2 MB
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Author(s)
Hwang, J.
Schwendeman, I.
Ihas, B. C.
Clark, Robert J.
Nikolou, M.
Argun, A.
Reynolds, J. R.
Tanner, D. B.
Cornick, Matthew T.
Date Issued
March 2011
Journal
Physical Review B
Publisher
American Physical Society (APS)
Citation
Hwang, J. et al. “In Situ Measurements of the Optical Absorption of Dioxythiophene-based Conjugated Polymers.” Physical Review B 83.19 (2011): n. pag. Web. 17 Feb. 2012. © 2011 American Physical Society
Version
Final published version
Abstract
Conjugated polymers can be reversibly doped by electrochemical means. This doping introduces new subband-gap optical absorption bands in the polymer while decreasing the band-gap absorption. To study this behavior, we have prepared an electrochemical cell allowing in situ measurements of the optical properties of the polymer. The cell consists of a thin polymer film deposited on gold-coated Mylar behind which is another polymer that serves as a counterelectrode. An infrared transparent window protects the upper polymer from ambient air. By adding a gel electrolyte and making electrical connections to the polymer-on-gold films, one may study electrochromism in a wide spectral range. As the cell voltage (the potential difference between the two electrodes) changes, the doping level of the conjugated polymer films is changed reversibly. Our experiments address electrochromism in poly(3,4-ethylenedioxythiophene) (PEDOT) and poly(3,4-dimethylpropylenedioxythiophene) (PProDOT-Me[subscript 2]). This closed electrochemical cell allows the study of the doping induced subband-gap features (polaronic and bipolaronic modes) in these easily oxidized and highly redox switchable polymers. We also study the changes in cell spectra as a function of polymer thickness and investigate strategies to obtain cleaner spectra, minimizing the contributions of water and gel electrolyte features.
MIT Department
Lincoln Laboratory
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DOI of Published Version
https://doi.org/10.1103/PhysRevB.83.195121
