Amplified Interfacial Effect in an Atomically Dispersed RuOx‐on‐Pd 2D Inverse Nanocatalyst for High‐Performance Oxygen Reduction
Atomically dispersed oxide‐on‐metal inverse nanocatalysts provide a blueprint to amplify the strong oxide–metal interactions for heterocatalysis but remain a grand challenge in fabrication. Here we report a 2D inverse nanocatalyst, RuOx‐on‐Pd nanosheets, by in situ creating atomically dispersed RuOx...
Gespeichert in:
Veröffentlicht in: | Angewandte Chemie 2021-07, Vol.133 (29), p.16229-16236 |
---|---|
Hauptverfasser: | , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
Zusammenfassung: | Atomically dispersed oxide‐on‐metal inverse nanocatalysts provide a blueprint to amplify the strong oxide–metal interactions for heterocatalysis but remain a grand challenge in fabrication. Here we report a 2D inverse nanocatalyst, RuOx‐on‐Pd nanosheets, by in situ creating atomically dispersed RuOx/Pd interfaces densely on ultrathin Pd nanosheets via a one‐pot synthesis. The product displays unexpected performance toward the oxygen reduction reaction (ORR) in alkaline medium, which represents 8.0‐ and 22.4‐fold enhancement in mass activity compared to the state‐of‐the‐art Pt/C and Pd/C catalysts, respectively, showcasing an excellent Pt‐alternative cathode electrocatalyst for fuel cells and metal–air batteries. Density functional theory calculations validate that the RuOx/Pd interface can accumulate partial charge from the 2D Pd host and subtly change the adsorption configuration of O2 to facilitate the O−O bond cleavage. Meanwhile, the d‐band center of Pd nanosubstrates is effectively downshifted, realizing weakened oxygen binding strength.
An atomically dispersed RuOx‐on‐Pd ultrathin 2D inverse nanocatalyst with amplified oxide/metal interface effects may serve as an excellent Pt‐alternative cathode electrocatalyst for fuel cells and metal–air batteries. |
---|---|
ISSN: | 0044-8249 1521-3757 |
DOI: | 10.1002/ange.202104013 |