Boosting Overall Water Splitting via FeOOH Nanoflake-Decorated PrBa0.5Sr0.5Co2O5+δ Nanorods
Source abstract
Abstract
The development of an efficient, robust, and low-cost catalyst for water electrolysis is critically important for renewable energy conversion. Herein, we achieve a significant improvement in electrocatalytic activity for both the oxygen-evolution reaction (OER) and the hydrogen-evolution reaction (HER) by constructing a novel hierarchical PrBa0.5Sr0.5Co2O5+δ (PBSC)@FeOOH catalyst. The optimized PBSC@FeOOH-20 catalyst consisted of layered perovskite PBSC nanorods and 20 nm thick amorphous FeOOH nanoflakes exhibiting an excellent electrocatalytic activity for the OER and the HER in 0.1 M KOH media, delivering a current density of 10 mA cm-2 at overpotentials of 390 mV for the OER and 280 mV for the HER, respectively. The substantially enhanced performance is probably attributed to the hierarchical nanostructure, the good charge-transfer capability, and the strong electronic interactions of FeOOH and PBSC. Importantly, an alkaline electrolyzer-integrated PBSC@FeOOH-20 catalyst as both the anode and cathode shows a highly active overall water splitting with a low voltage of 1.638 V at 10 mA cm-2 and high stability during continuous operation. This study provides new insights into exploring efficient bifunctional catalysts for overall water splitting, and it suggests that the rational design of the oxyhydroxide/perovskite heterostructure shows great potential as a promising type of electrocatalysts.
Source: europepmc · Quality: candidate unverified · Source record ↗
Research context
OpenAlex topics: Electrocatalysts for Energy Conversion · Advanced battery technologies research · Fuel Cells and Related Materials
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Faculty of Materials Science and Chemistry, China University of Geosciences, Wuhan 430074, China
Funding
National Natural Science Foundation of China
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