skip to main content
OSTI.GOV title logo U.S. Department of Energy
Office of Scientific and Technical Information

Title: In situ Fourier transform infrared spectroscopic studies on a metal complex-immobilized polyaniline/Prussian blue-modified electrode and the application to the electroreduction of CO{sub 2}

Journal Article · · Journal of the Electrochemical Society
DOI:https://doi.org/10.1149/1.1837260· OSTI ID:428168
; ;  [1]
  1. Yamaguchi Univ., Ube (Japan). Dept. of Applied Chemistry

In situ Fourier transform infrared spectroscopic studies have been carried out on the nature of a metal complex-immobilized polyaniline (PAn)/Prussian blue-modified electrode and on the application of this electrode to the electroreduction of CO{sub 2} in an aqueous solution. On cathodic polarization, the ring structures of PAn transformed from quinoid to benzenoid states. It was confirmed that the metal complex [1,8-dihydroxynaphthalene-3,6-disulfonato iron (II)] once doped onto the conducting polymer is not undoped in cathodic processes, and the charge balance of the polymer is kept by taking an electrolyte cation in or out. The onset potential where CO{sub 2} was accumulated with the modified electrode was 0 V vs. Ag/AgCl, and the amount of CO{sub 2} on the electrode became largest at {minus}0.2 V. The accumulation of CO{sub 2} with the electrode mediator was caused by the bonding between the mediated PAn and CO{sub 2} through a linkage of the electrophilic carbon atom of CO{sub 2} with the nitrogen atom of the benzenoid ring. The prolonged electrolysis of CO{sub 2} at potentials more negative than {minus}0.3 V led to the generation of C{sub 1} {approximately} C{sub 3} species involving lactic and formic acids, and the scheme of the initial reduction process was disclosed.

Sponsoring Organization:
USDOE
OSTI ID:
428168
Journal Information:
Journal of the Electrochemical Society, Vol. 143, Issue 11; Other Information: PBD: Nov 1996
Country of Publication:
United States
Language:
English