Abstract
The present work compares two degradation approaches for organics molecules on TiO2 by (i) classical photocatalysis and (ii) anodic-breakdown (AB) catalysis. For this, TiO2 layers prepared by electrochemical anodization and annealing were used for the decomposition of crystal violet. AB-catalysis was performed at various applied potentials and the degradation kinetics and products were analysed. From the present results one can deduce that a valence band hole ejection mechanism is operative for AB catalysis and photocatalysis. We explain AB catalysis in terms of a Fowler–Nordheim type of junction breakdown model.