Abstract

This study demonstrates, with C16O2/C18O2 isotope switch and H2-TPR experiments, for the first time that (i) the high-temperature water–gas shift (HT-WGS) reaction by copper–chromium-iron oxide catalysts follows a redox mechanism dominated by the surface layer, (ii) the number of catalytic active sites can be quantified by the isotopic switch, and (iii) the turnover frequency (TOF) can be determined from knowledge of the number of sites. The quantitative TOF values reveal that chromium is only a textural promoter, whereas copper is a chemical promoter.

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