IrO2 and boron-doped diamond electrodes have been tested by preparative ele
ctrolysis of simple model compounds in acid medium. It was confirmed that i
n oxidation reactions of more complex mechanism than simple electron transf
er, these electrodes are active only at potentials of simultaneous oxygen e
volution. At IrO2 electrodes, the reaction is mediated by chemisorbed oxyge
n, probably forming IrO3-type active sites, and yields highly selective oxi
dation products at low overpotentials and with moderate current efficiency.
At diamond electrodes, mediation at high overpotentials is due to physisor
bed . OH radicals leading to complete combustion of the organic compound wi
th high current efficiency. (C) 1999 The Electrochemical Society. S1099-006
2(98)11-115-X. All rights reserved.