Electronic Structure Engineering of Single-Atom Ru Sites via Co-N4 Sites for Bifunctional pH-Universal Water Splitting

© 2022 The Authors. Advanced Materials published by Wiley-VCH GmbH.

Bibliographische Detailangaben
Veröffentlicht in:Advanced materials (Deerfield Beach, Fla.). - 1998. - 34(2022), 21 vom: 19. Mai, Seite e2110103
1. Verfasser: Rong, Chengli (VerfasserIn)
Weitere Verfasser: Shen, Xiangjian, Wang, Yuan, Thomsen, Lars, Zhao, Tingwen, Li, Yibing, Lu, Xunyu, Amal, Rose, Zhao, Chuan
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2022
Zugriff auf das übergeordnete Werk:Advanced materials (Deerfield Beach, Fla.)
Schlagworte:Journal Article electrochemical energy conversion hydrogen ruthenium cobalt single-atom catalysts water splitting
Beschreibung
Zusammenfassung:© 2022 The Authors. Advanced Materials published by Wiley-VCH GmbH.
The development of bifunctional water-splitting electrocatalysts that are efficient and stable over a wide range of pH is of great significance but challenging. Here, an atomically dispersed Ru/Co dual-sites catalyst is reported anchored on N-doped carbon (Ru/Co-N-C) for outstanding oxygen evolution reaction (OER) and hydrogen evolution reaction (HER) in both acidic and alkaline electrolytes. The Ru/Co-N-C catalyst requires the overpotential of only 13 and 23 mV for HER, 232 and 247 mV for OER to deliver a current density of 10 mA cmgeo -2 in 0.5 m H2 SO4 and 1 m KOH, respectively, outperforming benchmark catalysts Pt/C and RuO2 . Theoretical calculations reveal that the introduction of Co-N4 sites into Ru/Co-N-C efficiently modify the electronic structure of Ru by enlarging Ru-O covalency and increasing Ru electron density, which in turn optimize the bonding strength between oxygen/hydrogen intermediate species with Ru sites, thereby enhancing OER and HER performance. Furthermore, the incorporation of Co-N4 sites induces electron redistribution around Ru-N4, thus enhancing corrosion-resistance of Ru/Co-N-C during acid and alkaline electrolysis. The Ru/Co-N-C has been applied in a proton exchange membrane water electrolyzer and steady operation is demonstrated at a high current density of 450 mA cmgeo -2 for 330 h
Beschreibung:Date Revised 26.05.2022
published: Print-Electronic
Citation Status PubMed-not-MEDLINE
ISSN:1521-4095
DOI:10.1002/adma.202110103