Bifunctional Water-Splitting Electrocatalysis Achieved by Defect Order in LaA2Fe3O8 (A = Ca, Sr)
Source abstract
Abstract
We report the utilization of defect order for development of a bifunctional oxide electrocatalyst. This structure–activity relationship is demonstrated through a disorder–order transformation in LaA2Fe3O8 (A = Ca, Sr). The defect-ordered oxide, LaCa2Fe3O8, shows electrocatalytic activity for oxygen evolution reaction, on par with that of the state-of-the-art precious metal catalyst RuO2. In addition, it is capable of catalyzing the other half-reaction of water-splitting, namely the hydrogen evolution reaction. Importantly, it is an iron-based catalyst and can be used as a single phase bulk material. The most important aspect of this work is the pronounced impact of defect order on the electrocatalytic properties of oxides.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Electrocatalysts for Energy Conversion · Advanced battery technologies research · Electrochemical Analysis and Applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Chemistry, University of Louisville, Louisville, Kentucky 40292, United States
Institute of Electronic Structure and Laser, FORTH, Heraklion, Crete 71110, Greece
Conn Center for Renewable Energy Research, University of Louisville, Louisville, Kentucky 40292, United States
Department of Physics and Astronomy, University of Kentucky, Lexington, Kentucky 40506, United States
Funding
National Science Foundation
References (31)
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