Abstract
In this work, a series of La1-xSrxMnO3 catalysts for CO oxidation were successfully fabricated via a facile sol-gel method with multistage calcination. By modifying the Sr doping quantity at A-site, the surface Mn4+/ Mn3+ ratio was manipulated, and thus lattice oxygen and oxygen vacancy concentrations of were further regulated by the system electron migration. This domino effect produced a radically different catalytic response, of which the optimal La0.4Sr0.6MnO3 samples performed the most excellent CO oxidation at lower temperature window. In-situ DRFITS spectra revealed catalytic intermediates and demonstrated the concurrence of dominant Mv-K mechanism and secondary E-R reaction pathway in CO oxidation over La0.4Sr0.6MnO3 under three types of thermodynamic states. The study is poised to enhance the propagation and practical employment of Sr-doped LaMnO3 perovskite catalysts, while supplying theoretical perspectives for the investigation towards underlying CO reaction mechanisms.
| Original language | English |
|---|---|
| Article number | 114938 |
| Journal | Journal of Environmental Chemical Engineering |
| Volume | 12 |
| Issue number | 6 |
| DOIs | |
| State | Published - Dec 2024 |
Keywords
- CO oxidation
- LaSrMnO
- Lattice oxygen
- Mv-K mechanism
- Oxygen vacancy
- Thermal catalysis