Oxygen-Pressure-LimitedRecovery of the Hematite α-Fe2O3(0001) Surface from a Reduced Fe3O4(111)-likeLayer

Abstract The oxidation kinetics of hematite α-Fe2O3(0001) surfaces are vital for its applications in catalysis, environmental remediation, and industrial processes. Despite prior studies, the roles of temperature, oxygen partial pressure, and oxygen chemical potential in controlling nucleation and growth kinetics are not fully understood. Using real-time Low Energy Electron Microscopy/Diffraction (LEEM/LEED), we systematically investigate the oxidation of a reduced Fe3O4(111)-like surface layer to hematite under controlled conditions. We show that complete recovery of the hematite surface termination is closely linked to the nucleation and lateral growth of a two-dimensional honeycomb (H) phase. H-phase nucleation and growth do not follow standard Arrhenius kinetics. A set of experiments comprising oxidation at constant oxygen partial pressure, constant temperature, and constant chemical potential, while varying temperature, pressure, or both, indicates that oxygen supply limits the H-phase growth rate. Under constant oxygen partial pressure pO2, increasing the temperature accelerates nucleation but decelerates the growth rate of the H-phase. The growth dramatically slows for pO2 < ∼2 × 10–6 mbar. Keeping the oxygen chemical potential constant, i.e., regulating both pO2 and temperature to keep the thermodynamic driving force provides increasing growth rates with increasing temperature only if pO2 > ∼2 × 10–6 mbar. Our study thus elucidates the interplay between thermodynamics and kinetics in hematite surface oxidation, informing strategies to optimize surface properties for catalytic and industrial processes.