We investigate the electrochemical behavior of some model organic compounds
on boron-doped synthetic diamond thin film electrodes, obtained by HF CVD
on p-Si substrate. The obtained results have shown that only reactions invo
lving simple electron transfer like hydroquinone/benzoquinone are active in
the potential region of the supporting electrolyte stability, although thi
s system is irreversible on diamond electrodes. For oxidation reactions wit
h more complex mechanism, diamond electrodes show no electrocatalytic activ
ity in the potential region of the supporting electrolyte stability. These
complex oxidation reactions can take place on diamond electrodes in the pot
ential region of the supporting electrolyte decomposition. The reactivity o
f some alcohols and carboxylic acids is studied by cyclic voltammetry. Isop
ropanol in 1 M H2SO4 is oxidized on diamond anode at a constant current den
sity and the intermediates formed are analyzed by HPLC. Finally, a simplifi
ed mechanism for the oxidation of organics by electrogenerated OH. radicals
on diamond is proposed.