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Updated: Apr 18, 2026

Probing and Mapping Electrode Surfaces in Solid Oxide Fuel Cells
Published on: September 20, 2012
Surface interrogation of CoP(i) water oxidation catalyst by scanning electrochemical microscopy
1Center for Electrochemistry, Department of Chemistry, The University of Texas at Austin , Austin, Texas 78712, United States.
Abstract:
Despite exhaustive spectroscopic investigations on the CoPi oxygen-evolving catalyst over the past several years, little is known about the surface cobalt sites and intermediates in direct contact with water that are responsible for the actual catalysis. Many studies thus far have been limited to ex situ characterizations or bulk film measurements, often in the absence of solvent. Here we describe an investigation of the CoPi catalyst by surface interrogation scanning electrochemical microscopy (SI-SECM). This method should allow us to selectively study surface atoms separately from the bulk in a solvent-filled environment. By SI-SECM, independent titrations of surface Co(III) and Co(IV) were performed, yielding a direct measurement of the surface active-site density of a CoPi electrode (11 Co/nm(2)). The pseudo-first-order reaction rate constants of Co(III) and Co(IV) with water were determined to be 0.19 and >2 s(-1), respectively, through time-dependent titration measurements.
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