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.

Noble metal aerogels (NMAs) are an emerging class of porous materials. Embracing nano‐sized highly‐active noble metals and porous structures, they display unprecedented performance in diverse electrocatalytic processes. However, various impurities, particularly organic ligands, are often involved in the synthesis and remain in the corresponding products, hindering the investigation of the intrinsic electrocatalytic properties of NMAs. Here, starting from laser‐generated inorganic‐salt‐stabilized metal nanoparticles, various impurity‐free NMAs (Au, Pd, and Au‐Pd aerogels) were fabricated. In this light, we demonstrate not only the intrinsic electrocatalytic properties of NMAs, but also the prominent roles played by ligands in tuning electrocatalysis through modulating the electron density of catalysts. These findings may offer a new dimension to engineer and optimize the electrocatalytic performance for various NMAs and beyond.

Pulsed laser postprocessing (PLPP) of colloidal nanoparticles and related laser fragmentation in liquid (LFL) using a liquid jet setup have become an acknowledged tool to reduce the nanoparticle diameter down to a few nanometers, alter the crystal phase, or increase the defect density under high-purity and continuous-flow conditions. In recent studies on LFL that were conducted with a cylindrical liquid jet, intensity gradients and related incomplete illumination of the volume element passing through the laser beam path were reported to cause a broadening of the product particle size distribution, melting, and phase segregation. In this paper, we present a new flat jet design, which reduces the deviation of the laser intensity up to 10 times compared to the conventional cylindrical liquid jet. The experimental threshold intensity for gold nanoparticle fragmentation found with the cylindrical setup strongly deviates from the theoretical prediction, while they are in very good agreement for the flat jet setup. Additionally, a narrow product size fraction of 3 ± 2 nm was found for the flat jet, while the main product fraction gained from the cylindrical jet was 10 ± 8 nm in size under the same conditions. Consequently, the flat jet setup allows us not only to study laser fragmentation mechanisms with higher precision but also to gain product particles with narrow particle size distribution at single pulse per particle conditions even at elevated mass concentrations (>50 mg L −1 ). In future studies, these promising results also render the flat jet setup relevant for the other disciplines of PLPP such as laser melting and defect engineering.

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.

Noble metal aerogels (NMAs) are an emerging class of porous materials. Embracing nano‐sized highly‐active noble metals and porous structures, they display unprecedented performance in diverse electrocatalytic processes. However, various impurities, particularly organic ligands, are often involved in the synthesis and remain in the corresponding products, hindering the investigation of the intrinsic electrocatalytic properties of NMAs. Here, starting from laser‐generated inorganic‐salt‐stabilized metal nanoparticles, various impurity‐free NMAs (Au, Pd, and Au‐Pd aerogels) were fabricated. In this light, we demonstrate not only the intrinsic electrocatalytic properties of NMAs, but also the prominent roles played by ligands in tuning electrocatalysis through modulating the electron density of catalysts. These findings may offer a new dimension to engineer and optimize the electrocatalytic performance for various NMAs and beyond.