Oxygen isotope was used to investigate the active electrochemical reaction
site on a solid oxide electrolyte. The isotope exchange reaction was perfor
med under current flow, and the distribution of the incorporated isotope wa
s analyzed by a secondary ion mass spectrometer. The results were compared
with calculations using a simple model. The lateral resolution of the prese
nt method was estimated to be around 1 mu m. The quenching process and the
imaging resolution should be improved to investigate further details. (C) 2
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