Abstract
Ce‐rich mixed metal oxides comprise a recently discovered class of electrocatalysts for the oxygen evolution reaction (OER). In particular, at current densities below 10 mA cm−2, Ni0.3Fe0.07Co0.2Ce0.43Ox exhibits superior activity compared to the corresponding transition metal oxides, despite the relative inactivity of ceria. To elucidate the enhanced activity and underlying catalytic mechanism, detailed structural characterization of this quinary oxide electrocatalyst is reported. Transmission electron microscopy imaging of cross‐section films as‐prepared and after electrochemical testing reveals a stable two‐phase nanostructure composed of 3–5 nm diameter crystallites of fluorite CeO2 intimately mixed with 3–5 nm crystallites of transition metal oxides alloyed in the rock salt NiO structure. Dosing experiments demonstrate that an electron flux greater than ≈1000 e Å−2 s−1 causes the inherently crystalline material to become amorphous. A very low dose rate of 130 e Å−2 s−1 is employed for atomic resolution imaging using inline holography techniques to reveal a nanostructure in which the transition metal oxide nanocrystals form atomically sharp boundaries with the ceria nanocrystals, and these results are corroborated with extensive synchrotron X‐ray absorption spectroscopy measurements. Ceria is a well‐studied cocatalyst for other heterogeneous and electrochemical reactions, and our discovery introduces biphasic cocatalysis as a design concept for improved OER electrocatalysts.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
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.