The effect of pretreatment conditions on the N2O-decomposition activity of Fe-ZSM-5 prepared by chemical vapor deposition (CVD) was studied by steady-state kinetics and step-response experiments. Pretreatment at 873 K in H-2 or He significantly increased the N2O-decomposition activity of Fe-ZSM-5 CVD. In addition to the increased steady-state activity, the catalyst exhibited a very high initial activity in the step-response experiments, which slowly decayed to steady state. This "transient" activity was particularly high after pretreatment of the samples in He, whereas it vanished completely after pretreatment in O-2 or exposure to water vapor. This led to the conclusion that the transient activity is related to strongly dehydroxylated Fe2+ sites created by autoreduction at high temperatures. On the basis of isotope-labeling data a mechanism for N2O decomposition is proposed. The first step is the reaction of Fe2+ with N2O to give a Fe3+-O-species, which quickly transforms into a Fe2+-peroxo complex. Desorption Of O-2 occurs upon reaction of the Fe2+ -O-2(2-) complex with another N2O molecule (mainly during the transient) or via the recombination of two peroxo species after their migration over the iron oxide cluster (mainly during steady state). (C) 2004 Elsevier Inc. All rights reserved.