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Impact of Single-Pulse, Low-Intensity Laser Post-Processing on Structure and Activity of Mesostructured Cobalt Oxide for the Oxygen Evolution Reaction

[Image: see text] 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 diff...

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Detalles Bibliográficos
Autores principales: Budiyanto, Eko, Zerebecki, Swen, Weidenthaler, Claudia, Kox, Tim, Kenmoe, Stephane, Spohr, Eckhard, DeBeer, Serena, Rüdiger, Olaf, Reichenberger, Sven, Barcikowski, Stephan, Tüysüz, Harun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2021
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8587604/
https://www.ncbi.nlm.nih.gov/pubmed/34323466
http://dx.doi.org/10.1021/acsami.1c08034
Descripción
Sumario:[Image: see text] 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 X-ray 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 defect-induced 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.