Looping metal-support interaction in heterogeneous catalysts during redox reactions
Yue Pan1,2, Shiyu Zhen3, Xiaozhi Liu1
1Beijing National Laboratory for Condensed Matter Physics, Institute of Physics, Chinese Academy of Sciences, Beijing, China.
This study reveals a dynamic looping interaction at nickel-iron (NiFe) and iron oxide (Fe3O4) catalyst interfaces during hydrogen oxidation. This unique mechanism involves migrating interfaces and spatially separated reactions, enhancing catalytic performance.
Area of Science:
- Heterogeneous catalysis
- Materials science
- Surface chemistry
Background:
- Metal-support interfaces are crucial for heterogeneous catalyst performance.
- Understanding dynamic interactions at the atomic level is key to catalyst design.
Purpose of the Study:
- To investigate the metal-support interactions in NiFe-Fe3O4 catalysts during the hydrogen oxidation reaction.
- To elucidate the atomic-scale dynamics governing catalytic activity.
Main Methods:
- Operando transmission electron microscopy (TEM) was employed to observe catalyst behavior under reaction conditions.
- In-situ analysis allowed for the visualization of dynamic interface changes.
Main Results:
- A looping metal-support interaction was identified at the NiFe-Fe3O4 interfaces.
- Lattice oxygens reacted with hydrogen, leading to dynamically migrating interfaces.
- Reduced iron atoms migrated and reacted with oxygen molecules, coupling reactions.
- Hydrogen oxidation and support redox reactions were intrinsically coupled via interface migration.
Conclusions:
- The study provides novel mechanistic insights into metal-support interactions.
- Dynamic interface migration plays a critical role in the catalytic cycle.
- Operando TEM is a powerful tool for studying atomic-scale dynamics in catalysis.
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