Self-Anticoking of a Cobalt Surface by Subsurface Oxygen in the Fischer-Tropsch Synthesis
Lingshun Xu1, Yuekang Jin1, Zongfang Wu1
1Hefei National Laboratory for Physical Sciences at Microscale, CAS Key Laboratory of Materials for Energy Conversion, Department of Chemical Physics, University of Science and Technology of China, Jinzhai Road 96, Hefei, 230026, P. R. China.
Abstract:
Understanding the fundamental processes taking place on Co surfaces during the Fischer-Tropsch (FT) synthesis is of great interest and importance. We herein report a self-anticoking mechanism of a cobalt surface by subsurface oxygen. The active carbidic carbon species for FT synthesis tends to transform into the inactive graphitic carbon species on clean Co(0001) and poisons the Co surface. Subsurface atomic oxygen on Co(0001) can stabilize the active carbidic carbon species and quench the transformation process. These results reveal, to the best of our knowledge, for the first time the reactivity of various surface species on Co surfaces that dynamically maintain a delicate balance to enhance the long-term stability of Co catalysts during FT synthesis.
More Related Videos
10:57Synthesis and Performance Characterizations of Transition Metal Single Atom Catalyst for Electrochemical CO2 Reduction
Published on: April 10, 2018
10:15Solar-Driven Electrochemical Green Fuel Production from CO2 and Water Using Ti3C2Tx MXene-Supported CuZn and NiCo Catalysts
Published on: November 7, 2025
Related Concept Videos
Oxidation of Alkenes: Syn Dihydroxylation with Potassium Permanganate
Oxidation of Alkenes: Syn Dihydroxylation with Osmium Tetraoxide
Oxidative Cleavage of Alkenes: Ozonolysis
Ozone is a symmetrical bent molecule stabilized by a resonance structure.
Catalysis
Oxidation of Alkenes: Anti Dihydroxylation with Peroxy Acids
Heterogeneous Catalysis
