| Literature DB >> 30360054 |
Zonghuai Zhang1, Beibei He1, Liangjian Chen1, Huanwen Wang1, Rui Wang1, Ling Zhao1, Yansheng Gong1.
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.Entities:
Keywords: double perovskite; electronic interactions; hydrogen-evolution reaction; overall water splitting; oxygen-evolution reaction
Year: 2018 PMID: 30360054 DOI: 10.1021/acsami.8b12372
Source DB: PubMed Journal: ACS Appl Mater Interfaces ISSN: 1944-8244 Impact factor: 9.229