Home > Publications database > Probing the Electrolyte Transfer in Ultrathin Polypyrrole Films by In Situ X-ray Reflectivity and Electrochemistry |
Journal Article | PUBDB-2020-04509 |
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2020
ACS Publ.
Washington, DC
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Please use a persistent id in citations: doi:10.1021/acs.langmuir.0c02068 doi:10.3204/PUBDB-2020-04509
Abstract: This study reports on the potential-induced chargeand mass transfer between an ultrathin polypyrrole (PPy)film andan electrolyte by simultaneous in situ X-ray reflectivity (XRR) andelectrochemistry (EC) utilizing their sensitivity to electrons. Anabout 30 nm thin PPyfilm was deposited on a silicon single crystalby fast potential cycling, providing a densefilm of an extraordinarysmall surface roughness. XRR was recorded from the PPyfilm inan aqueous 0.1 M perchloric acid at electric potentials between−0.2 V and +0.5 V vs Ag/AgCl. The PPyfilm shows typicalreversible and linear changes infilm thickness and electron densityarising from the potential-dependent electrolyte incorporation. Byintroducing EC-XRR, a comprehensive analysis combining in situ XRR and EC, the net number of electrons passing through thePPy-electrolyte interface was deduced along with the potential-induced thickness variations, indicating a complex exchangemechanism. Evidently, along with the anion transfer, parallel charge compensation by protons and a volume and electroncompensating counterflow of solvent molecules take place. Complementary time-dependent EC-XRR scans indicate that theseexchange mechanisms are individual in two potential ranges. The low actuation along with a high pseudocapacitance suggest the fastpotentiodynamically deposited PPyfilm as a promising supercapacitor material.
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