The Fischer–Tropsch product, water, is regularly hypothesized to be the driving force for catalyst deactivation. Cobalt nanoparticles may be oxidized to CoO, form mixed-metal oxides with supports, or sinter to larger particles. This Comment discusses the feasibility of these deactivation pathways, highlighting the importance of in situ characterization.
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Financial support from the DSI-NRF Centre of Excellence in Catalysis (c*change), the University of Cape Town (UCT), and the German Academic Exchange Service (DAAD) is gratefully acknowledged.
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Wolf, M., Fischer, N. & Claeys, M. Water-induced deactivation of cobalt-based Fischer–Tropsch catalysts. Nat Catal 3, 962–965 (2020). https://doi.org/10.1038/s41929-020-00534-5
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DOI: https://doi.org/10.1038/s41929-020-00534-5
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