4.6 Article

Plasmonic response of electrified metal-liquid interfaces during faradaic and non-faradaic reactions by enhanced optical transmission

Journal

ANALYST
Volume 137, Issue 17, Pages 3932-3939

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c2an35488h

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Funding

  1. U.S. National Science Foundation Water CAMPWS [CTS0120978]
  2. U.S. Department of Energy Basic Energy Sciences [DE FG02 07ER15851]

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Thin Au films, patterned by focused ion beam (FIB) milling to contain an array of subwavelength nanopores, exhibit enhanced optical transmission (EOT) via front-back resonance coupling. The films also serve as working electrodes capable of controlling the local potential, allowing electrochemical processes to be monitored using wavevector-resolved spectral mapping. The precise value of the surface plasmon resonance (SPR) wavevector can be extracted from the enhanced optical transmission signal and correlated with several distinct classes of electrochemical processes: double layer reorganization, faradaic adsorption/desorption, heterogeneous electron transfer, and anion adsorption. Specifically, the protonation/deprotonation reaction of an adsorbed monolayer of 4-mercaptobenzoic acid, the adsorption/desorption reaction of dodecanethiol to Au, the solution-phase reaction of ferriferrocyanide, and sulfate adsorption/desorption are investigated. A simple model is presented that encompasses both the EOT signal and electrochemical processes and produces semi-quantitative agreement with the SPR spectral wavevector mapping observed experimentally.

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