Synchrotron Infrared Radiation for Electrochemical External Reflection Spectroscopy: A Case Study Using Ferrocyanide

• Published in: Analytical chemistry (Washington) Vol. 83; no. 10; pp. 3632 - 3639
• Main Authors: Rosendahl, Scott M, Borondics, Ferenc, May, Tim E, Pedersen, Tor M, Burgess, Ian J
• Format: Journal Article
• Language: English
• Published: Washington, DC American Chemical Society 15.05.2011
• Subjects: Analytical chemistry; Chemistry; Diffusion; Electrocatalysis; Electrochemical methods; Electrochemical Techniques - methods; Electrodes; Exact sciences and technology; Ferrocyanides - chemistry; Infrared radiation; Oxidation-Reduction; Spectrometric and optical methods; Spectrophotometry, Infrared - instrumentation; Spectrophotometry, Infrared - methods; Spectrum analysis; Synchrotrons; Microscope; Noise; Electrochemical method; Size; Use; Time; Ultramicroelectrode; Case study; Reflection spectrometry; Time resolution; Volume; Infrared radiation; Hexacyanoferrates II; Limit; Diffusion; Comparative study; Synchrotron radiation; Reflectance; Signal to noise ratio
• ISSN: 0003-2700; 1520-6882
• DOI: 10.1021/ac200250s

Synchrotron infrared radiation has been successfully coupled through an infrared (IR) microscope to a thin-cavity external reflectance cell to study the diffusion controlled redox of a ferrocyanide solution. Excellent signal-to-noise ratios were achieved even at aperture settings close to the diffraction limit. Comparisons of noise levels as a function of aperture size demonstrate that this can be attributed to the high brilliance of synchrotron radiation relative to a conventional thermal source. Time resolved spectroscopic studies of diffusion controlled redox behavior have been measured and compared to purely electrochemical responses of the thin-cavity cell. Marked differences between the two measurements have been explained by analyzing diffusion in both the axial (linear) and radial dimensions. Whereas both terms contribute to the measured current and charge, only species that originate in the volume element above the electrode and diffuse in the direction perpendicular to the electrode surface are interrogated by IR radiation. Implications for the use of ultramicroelectrodes and synchrotron IR (SIR) to study electrochemical processes in the submillisecond time domain are discussed.