Abstract

The aqueous oxygen reduction reaction (ORR) has recently received increased attention due to its critical role in clean and sustainable energy-generation technologies, such as proton exchange membranes (PEM) fuel cells, alkaline fuel cells and Zn-air batteries. The sluggish kinetics associated with ORR result from multistep electron-transfer process. The slow kinetics are partially related to the O2 adsorption process onto the catalyst, which happens at the triple-phase boundary (TPB) of the electrocatalyst-electrolyte-oxygen interface. Hence, tremendous efforts have been devoted to improving the intrinsic properties of electrocatalysts such as active sites, electrical conductivity and porosity. Engineering the electrocatalyst's interfacial properties is another critical issue in ORR, however less described in the literature. The surface of the catalyst provides the microenvironment for the triple boundary interface reaction, which directly influences its electrocatalytic activity and the kinetics. This Minireview is a summary of the existing literature on manipulating the interfacial surface of non-precious metal catalysts at the triple point between the solid catalyst, the aqueous electrolyte and the O2 gas with the aim of improving the ORR efficiency. Various approaches towards improving the wettability and nanostructuring the catalyst surface to boost the activity of the surface-active sites and provide improved stability are discussed.

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.