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Synergistic ruthenium single-atom and nanoparticles in nickel as cooperative catalysts for the alkaline hydrogen evolution reaction

  • Gaëlle Khalil
  • , Marie Sophie Dias-Fernandes
  • , Sumit Bawari
  • , Linghui Li
  • , Chiddharth Muthuraj
  • , Florent Ducrozet
  • , Minkyoung Kwak
  • , Miguel Comesaña-Hermo
  • , Andrea Zitolo
  • , Stephan N. Steinmann
  • , Shannon W. Boettcher
  • , Cédric Tard
  • , Benedikt Lassalle-Kaiser
  • , Marion Giraud
  • , Jennifer Peron
  • Université Paris Diderot
  • CNRS
  • Synchrotron SOLEIL
  • Ecole Normale Supérieure de Lyon
  • Sorbonne Université
  • Berkeley College of Chemistry

Research output: Contribution to journalArticlepeer-review

Abstract

Efficient hydrogen evolution reaction (HER) catalysts that reduce the use of noble metals and can be synthesized on a large scale are essential for advancing anion exchange membrane water electrolyzers (AEMWEs) toward commercialization. Herein, we present a composite catalyst in which Ru nanoparticles coexist with Ru single-atom alloys (SAAs) dispersed within Ni nanoparticles (Ru-SAA/Ni), creating a highly active HER electrocatalyst. Using a one-pot and scalable synthesis method, we can tune the material composition from SAA, i.e. materials containing atomically dispersed Ru atoms (with ≤0.4 at% Ru) to composite structures in which SAAs coexist with Ru NPs. Comprehensive characterization using XPS, XAS, and TEM confirms Ru-SAA formation at a low Ru content and composite structures at higher contents. Electrochemical evaluations conducted in a three-electrode setup reveal that Ru-SAA/Ni composites achieve HER performance on par with that of Pt/C. Computational insights suggest that water dissociation is significantly faster at the Ru/Ni interface compared with that on extended surfaces. These active sites are thermodynamically as active as basal planes, preventing the excessive accumulation of reaction intermediates (H*, OH*). All these results highlight the synergistic interaction between Ru SAAs and Ru nanoparticles and their potential for large-scale applications with minimal use of precious metals. Finally, the materials are processed and tested in AEMWEs, achieving 1.85 V at 0.5 A cm−2 with a total noble metal loading of only 0.1 mg cm−2.

Original languageEnglish
Pages (from-to)9177-9189
Number of pages13
JournalNanoscale
Volume18
Issue number17
DOIs
Publication statusPublished - 7 May 2026
Externally publishedYes

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