| Literature DB >> 35266633 |
Shu-Chao Sun1,2, Hao Jiang1, Zi-Yao Chen1, Qing Chen3, Ming-Yuan Ma1, Liang Zhen1,2,3, Bo Song4, Cheng-Yan Xu2,3.
Abstract
We report the strong catalyst-support interaction in WC-supported RuO2 nanoparticles (RuO2 -WC NPs) anchored on carbon nanosheets with low loading of Ru (4.11 wt.%), which significantly promotes the oxygen evolution reaction activity with a η10 of 347 mV and a mass activity of 1430 A gRu -1 , eight-fold higher than that of commercial RuO2 (176 A gRu -1 ). Theoretical calculations demonstrate that the strong catalyst-support interaction between RuO2 and the WC support could optimize the surrounding electronic structure of Ru sites to reduce the reaction barrier. Considering the likewise excellent catalytic ability for hydrogen production, an acidic overall water splitting (OWS) electrolyzer with a good stability constructed by bifunctional RuO2 -WC NPs only requires a cell voltage of 1.66 V to afford 10 mA cm-2 . The unique 0D/2D nanoarchitectures rationally combining a WC support with precious metal oxides provides a promising strategy to tradeoff the high catalytic activity and low cost for acidic OWS applications.Entities:
Keywords: Acidic Water Splitting; Bifunctional Electrocatalysts; Supported Electrocatalysts; Transition Metal Carbide
Year: 2022 PMID: 35266633 DOI: 10.1002/anie.202202519
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336