Year-end Sale % OFF 
Abstract
AbstractDeveloping efficient electrocatalysts from the earth‐abundant transition‐metal family is a great challenge for overall water splitting. Herein, we developed an approach to regulate the morphology and electronic structure of α‐Co0.9Fe0.1(OH)x nanoplates, in which FeCl2 (as a precursor) plays a significant role under reflux conditions. The resulting 2D α‐Co0.9Fe0.1(OH)x nanoplates exhibit more accessible edge active sites and more high‐valence Co species to boost its intrinsic activity. Therefore, this electrocatalyst shows outstanding oxygen evolution reaction performance (with an overpotential of 225 mV at 10 mA cm−2 and a Tafel slope of 39 mV dec−1 and good stability) and excellent activity toward the hydrogen evolution reaction (with an overpotential of 122 mV at 10 mA cm−2) in 1M KOH solution. When employed as bifunctional electrocatalysts on both the anode and cathode for overall water splitting, α‐Co0.9Fe0.1(OH)x can afford 10 mA cm−2 at 1.62 V with long‐term stability. The one‐pot synthesis of 2D Fe‐doped transition‐metal hydroxide nanoplates enriched with abundant edge sites may provide a new strategy for fabricating efficient overall water splitting catalysts.
Published Version
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callDisclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
