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Updated: Feb 27, 2026

Synthesis and Performance Characterizations of Transition Metal Single Atom Catalyst for Electrochemical CO2 Reduction
Published on: April 10, 2018
Avoiding Self-Poisoning: A Key Feature for the High Activity of Au/Mg(OH)2 Catalysts in Continuous Low-Temperature CO
Yuchen Wang1, Daniel Widmann1, Felix Lehnert1
1Institute of Surface Chemistry and Catalysis, Ulm University, 89069, Ulm, Germany.
Abstract:
Au/Mg(OH)2 catalysts have been reported to be far more active in the catalytic low-temperature CO oxidation (below 0 °C) than the thoroughly investigated Au/TiO2 catalysts. Based on kinetic and in situ infrared spectroscopy (DRIFTS) measurements, we demonstrate that the comparatively weak interaction of Au/Mg(OH)2 with CO2 formed during the low-temperature reaction is the main reason for the superior catalyst performance. This feature enables rapid product desorption and hence continuous CO oxidation at temperatures well below 0 °C. At these temperatures, Au/TiO2 also catalyzes CO2 formation, but does not allow for CO2 desorption, which results in self-poisoning. At higher temperatures (above 0 °C), however, CO2 formation is rate-limiting, which results in a much higher activity for Au/TiO2 under these reaction conditions.
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