Abstract

Developing improved catalysts for the oxygen evolution reaction (OER) is a crucial step for advancing technology in renewable fuels, e.g. solar water splitting. In this work, we identify CoTiOx as a novel nonprecious metal catalyst for the OER and explore the effect of temperature treatments on its activity, structure, and electronic state. Using a simple and scalable sol-gel synthesis, this catalyst can be deposited on a wide variety of conductive substrates. Physical and electronic characterization of the most active CoTiOx catalyst, prepared at low temperature (150°C), reveals an amorphous thin film structure with an oxidation state similar to that of other active cobalt catalysts. Electrochemical testing and X-ray absorption spectroscopy show that the more active, amorphous catalysts undergo greater changes in oxidation state during OER than the less active, crystalline catalysts. Extended electrochemical testing shows that the catalysts are stable in basic electrolyte.

Full Text
Paper version not known

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 call

Disclaimer: 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.