TY - JOUR
T1 - Nanoscale Visualization and Multiscale Electrochemical Analysis of Conductive Polymer Electrodes
AU - Daviddi, Enrico
AU - Chen, Zhiting
AU - Beam Massani, Brooke
AU - Lee, Jaemin
AU - Bentley, Cameron L.
AU - Unwin, Patrick R.
AU - Ratcliff, Erin L.
N1 - Funding Information:
A portion of this work is supported by the National Science Foundation under grant award DMR-1608289 (Z.C. and E.L.R). This research used resources of the Advanced Light Source, which is a DOE Office of Science User Facility under contract no. DE-AC02-05CH11231. SINS data were collected on beamline 5-4 under the assistance of Hans A. Bechtel. Use of the Stanford Synchrotron Radiation Lightsource, SLAC National Accelerator Laboratory, is supported by the U.S. Department of Energy, Office of Science, Office of Basic Energy Sciences under contract no. DE-AC02-76SF00515. All Cypher AFM images and data were collected in the W. M. Keck Center for Nano-Scale Imaging in the Department of Chemistry and Biochemistry at the University of Arizona. The Cypher instrument purchase was supported by the National Science Foundation under grant no. 1337371. FT-IR instrument purchase was supported by Arizona Technology and Research Initiative Fund (A.R.S.§15-1648). E.D. acknowledges Lubrizol Ltd. and the Warwick Collaborative Postgraduate Research Scheme for funding. C.L.B. acknowledges financial support from the Ramsay Memorial Fellowship Trust. P.R.U. gratefully acknowledges support from a Royal Society Wolfson Research Merit Award.
Publisher Copyright:
© 2019 American Chemical Society.
PY - 2019
Y1 - 2019
N2 - Conductive polymers are exceptionally promising for modular electrochemical applications including chemical sensors, bioelectronics, redox-flow batteries, and photoelectrochemical systems due to considerable synthetic tunability and ease of processing. Despite well-established structural heterogeneity in these systems, conventional macroscopic electroanalytical methods-specifically cyclic voltammetry-are typically used as the primary tool for structure-property elucidation. This work presents an alternative correlative multimicroscopy strategy. Data from laboratory and synchrotron-based microspectroscopies, including conducting-atomic force microscopy and synchrotron nanoscale infrared spectroscopy, are combined with potentiodynamic movies of electrochemical fluxes from scanning electrochemical cell microscopy (SECCM) to reveal the relationship between electrode structure and activity. A model conductive polymer electrode system of tailored heterogeneity is investigated, consisting of phase-segregated domains of poly(3-hexylthiophene) (P3HT) surrounded by contiguous regions of insulating poly(methyl methacrylate) (PMMA), representing an ultramicroelectrode array. Isolated domains of P3HT are shown to retain bulk-like chemical and electronic structure when blended with PMMA and possess approximately equivalent electron-transfer rate constants compared to pure P3HT electrodes. The nanoscale electrochemical data are used to model and predict multiscale electrochemical behavior, revealing that macroscopic cyclic voltammograms should be much more kinetically facile than observed experimentally. This indicates that parasitic resistances rather than redox kinetics play a dominant role in macroscopic measurements in these conductive polymer systems. SECCM further demonstrates that the ambient degradation of the P3HT electroactivity within P3HT/PMMA blends is spatially heterogeneous. This work serves as a roadmap for benchmarking the quality of conductive polymer films as electrodes, emphasizing the importance of nanoscale electrochemical measurements in understanding macroscopic properties.
AB - Conductive polymers are exceptionally promising for modular electrochemical applications including chemical sensors, bioelectronics, redox-flow batteries, and photoelectrochemical systems due to considerable synthetic tunability and ease of processing. Despite well-established structural heterogeneity in these systems, conventional macroscopic electroanalytical methods-specifically cyclic voltammetry-are typically used as the primary tool for structure-property elucidation. This work presents an alternative correlative multimicroscopy strategy. Data from laboratory and synchrotron-based microspectroscopies, including conducting-atomic force microscopy and synchrotron nanoscale infrared spectroscopy, are combined with potentiodynamic movies of electrochemical fluxes from scanning electrochemical cell microscopy (SECCM) to reveal the relationship between electrode structure and activity. A model conductive polymer electrode system of tailored heterogeneity is investigated, consisting of phase-segregated domains of poly(3-hexylthiophene) (P3HT) surrounded by contiguous regions of insulating poly(methyl methacrylate) (PMMA), representing an ultramicroelectrode array. Isolated domains of P3HT are shown to retain bulk-like chemical and electronic structure when blended with PMMA and possess approximately equivalent electron-transfer rate constants compared to pure P3HT electrodes. The nanoscale electrochemical data are used to model and predict multiscale electrochemical behavior, revealing that macroscopic cyclic voltammograms should be much more kinetically facile than observed experimentally. This indicates that parasitic resistances rather than redox kinetics play a dominant role in macroscopic measurements in these conductive polymer systems. SECCM further demonstrates that the ambient degradation of the P3HT electroactivity within P3HT/PMMA blends is spatially heterogeneous. This work serves as a roadmap for benchmarking the quality of conductive polymer films as electrodes, emphasizing the importance of nanoscale electrochemical measurements in understanding macroscopic properties.
KW - electrochemistry
KW - electron-transfer kinetics
KW - parasitic resistances
KW - poly(3-hexylthiophene)
KW - polymer degradation
KW - scanning electrochemical cell microscopy
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U2 - 10.1021/acsnano.9b06302
DO - 10.1021/acsnano.9b06302
M3 - Article
C2 - 31674763
AN - SCOPUS:85074867537
SN - 1936-0851
JO - ACS Nano
JF - ACS Nano
ER -