Herein, we report nanosecond, single-pulse laser post-processing (PLPP) in a liquid flat jet with precise control of the applied laser intensity to tune structure, defect sites, and the oxygen evolution reaction (OER) activity of mesostructured Co 3 O 4 . High-resolution X-ray diffraction (XRD), Raman, and Xray photoelectron spectroscopy (XPS) are consistent with the formation of cobalt vacancies at tetrahedral sites and an increase in the lattice parameter of Co 3 O 4 after the laser treatment. X-ray absorption spectroscopy (XAS) and X-ray emission spectroscopy (XES) further reveal increased disorder in the structure and a slight decrease in the average oxidation state of the cobalt oxide. Molecular dynamics simulation confirms the surface restructuring upon laser post-treatment on Co 3 O 4 . Importantly, the defectinduced PLPP was shown to lower the charge transfer resistance and boost the oxygen evolution activity of Co 3 O 4 . For the optimized sample, a 2-fold increment of current density at 1.7 V vs RHE is obtained and the overpotential at 10 mA/cm 2 decreases remarkably from 405 to 357 mV compared to pristine Co 3 O 4 . Post-mortem characterization reveals that the material retains its activity, morphology, and phase structure after a prolonged stability test.

Due to the variability of the cation occupancy of octahedral and tetrahedral sites, spinel ferrites and cobaltites are particularly interesting to investigate activity trends in oxidation catalysis. Yet, the preparation of the respective catalyst series remains challenging. We employed pulsed laser defect engineering of CoFe2O4 nanoparticles in water to gradually alter the cation occupancy of octahedral and tetrahedral sites by single laser pulses and study its effect on cinnamyl alcohol oxidation. Three CoFe2O4 catalysts from different synthesis methods resembling different initial site occupancy were chosen as starting materials. The laser‐induced randomization of the cation occupancy was verified by Mössbauer spectroscopy and linearly correlated with the conversion of cinnamyl alcohol while the size and Co : Fe ratio was maintained during laser processing. The study solidifies the importance of octahedral Co3+‐sites and the feasibility of pulsed laser processing for altering the cation occupancy and related crystallographic defect density in oxidation catalysis.

The spinel Co3O4 has many beneficial properties for potential use in catalysis. In operando, water is always present and alters the properties of the catalyst. We have used ab initio molecular dynamics to understand the effect of water and solvation on the structure and reactivity of the Co3O4 (001) A-type and B-type surface terminations. Water adsorbs on both terminations via a partial dissociative mode, and the A-termination is seen to be more reactive. On this surface, a higher degree of dissociation is observed in the topmost layers of the crystal in contact with water. Water dissociates more frequently on the Co2+ sites (about 75%) than on the adjacent Co3+ sites, where the degree of dissociation is about 50%. Increasing water coverage does not change the degree of water dissociation significantly. OH− adsorption on the Co2+ sites leads to a reduction of the amount of reconstruction and relaxation of the surface relative to the clean surface at room temperature. Proton transfer within the water films and between water molecules and surface has localized character. The B-terminated interface is less dynamic, and water forms epitactic layers on top of the Co3+ sites, with a dissociation degree of about 25% in the contact layer.

Co3O4, MgCo2O4 and MgO materials have been synthesized using a simple co-precipitation approach and systematically characterized. The total conversion of toluene to CO2 and H2O over spinel MgCo2O4 with wormlike morphology has been investigated. Compared with single metal oxides (Co3O4 and MgO), MgCo2O4 with the highest activity has exhibited almost 100% oxidation of toluene at 255 °C. The obtained results are analogous to typical precious metal supported catalysts. The activation energy of toluene over MgCo2O4 (38.5 kJ/mol) is found to be much lower than that of Co3O4 (68.9 kJ/mol) and MgO ((87.8 kJ/mol)). Compared with the single Co and Mg metal oxide, the as-prepared spinel MgCo2O4 exhibits a larger surface area, highest absorbed oxygen and more oxygen vacancies, thus highest mobility of oxygen species due to its good redox capability. Furthermore, the samples specific surface area, low-temperature reducibility and surface adsorbed oxygenated species ratio decreased as follows: MgCo2O4 > Co3O4 > MgO; which is completely in line with the catalytic performance trends and constitute the reasons for MgCo2O4 high excellent activity towards toluene total oxidation. The overall finding supported by ab initio molecular dynamics simulations of toluene oxidation on the Co3O4 and MgCo2O4 suggest that the catalytic process follows a Mars–van Krevelen mechanism.

CoFe2O4 is a promising catalytic material for many chemical reactions. We used ab initio molecular dynamic simulations to study the structure and reactivity of the A- and B-terminations of the low-index CoFe2O4(001) surfaces to water adsorption at room temperature. Upon adsorption, water partly dissociates on both termination with a higher dissociation degree on the A-termination (30% versus 19%). The 2-fold coordinated Fe3+(tet) in the tetrahedral voids and the 5-fold coordinated Fe3+(oct) in the octahedral voids are the main active sites for water dissociation on the A- and B-termination, respectively. Molecular water, hydroxydes, and surface OH resulting from proton transfer to surface oxygens are present on the surfaces. Both water-free surface terminations undergo reconstruction. The outermost Fe3+(tet) on the A-termination and B-termination move towards the nearby unoccupied octahedral voids. In the presence of a thin film of 32 water molecules, the reconstructions are partially and completely lifted on the A- and B-termination, respectively.