How the Arrangement of Platinum Atoms on Ruthenium Nanoparticles Improves Hydrogen Evolution Activity

Q Qinyu Li S Soshan Cheong (Electron Microscope Unit, Mark Wainwright Analytical Centre) A Agus R. Poerwoprajitno (Center for Integrated Nanotechnologies) S Shuting Xiang (Department of Materials Science and Chemical Engineering) A Anatoly I. Frenkel (Department of Materials Science and Chemical Engineering) Y Yuwei Yang (School of Chemical Engineering) N Nicholas M. Bedford (School of Chemical Engineering) S Sohaib Umer (School of Chemistry University of New South Wales Sydney NSW 2052 Australia) M Martina Lessio (School of Chemistry University of New South Wales Sydney NSW 2052 Australia) I Ichiro Ohnishi (JEOL Ltd. 3‐1‐2 Musashino, Akishima Tokyo 196‐8558 Japan) Z Zeno R. Ramadhan (Electron Microscope Unit, Mark Wainwright Analytical Centre) D Dale L. Huber (Center for Integrated Nanotechnologies Sandia National Laboratories Albuquerque NM 87185 USA) L Liming Dai (ARC Centre of Excellence for Carbon Science and Innovation) W Wolfgang Schuhmann (Analytical Chemistry – Center For Electrochemical Sciences (CES); Faculty of Chemistry and Biochemistry Ruhr University Bochum, Universitätsstr. 150 Bochum Germany) J J. Justin Gooding (School of Chemistry) R Richard D. Tilley (School of Chemistry)

Abstract

AbstractThe platinum‐ruthenium (PtRu) system is highly active for hydrogen evolution reaction (HER) in alkaline media with both Pt and Ru playing active roles in the water dissociation step that generates adsorbed hydrogen atoms. Precise control of the arrangement of Pt atoms on Ru nanoparticles can maximize the Pt‐Ru sites for water dissociation and Pt‐Pt sites for hydrogen production and can considerably improve HER catalytic performance. By directing the growth and distribution of Pt on Ru hourglass nanoparticles, the arrangement of Pt on Ru is controlled into forming Pt islands, small Pt clusters, and strings of a few Pt atoms. Calculations show that the unique atomic string arrangements of Pt on Ru is the thermodynamically favorable configuration. Additionally, these strings have a favorable combination of Pt‐Ru and Pt‐Pt sites, making the Pt‐string on Ru the most active catalyst with a more than fivefold increase in turnover frequency for alkaline HER compared to the Pt‐island on Ru catalyst. The results show how controlling the Pt atomic arrangement on Ru nanoparticle surfaces for the tuning of Pt‐Pt and Pt‐Ru neighboring sites can direct toward a more efficient HER mechanism and thereby significantly enhancing HER performance.

Article Details

Volume / Issue Vol. 37, Issue 41
Published October 01, 2025
ISSN 0935-9648
Publisher Unknown Publisher

Journal Info

Advanced Materials

Unknown Publisher

ISSN: 0935-9648 Physical Sciences

Authors (16)

Q

Qinyu Li

S

Soshan Cheong

Electron Microscope Unit, Mark Wainwright Analytical Centre

A

Agus R. Poerwoprajitno

Center for Integrated Nanotechnologies

S

Shuting Xiang

Department of Materials Science and Chemical Engineering

A

Anatoly I. Frenkel

Department of Materials Science and Chemical Engineering

Y

Yuwei Yang

School of Chemical Engineering

N

Nicholas M. Bedford

School of Chemical Engineering

S

Sohaib Umer

School of Chemistry University of New South Wales Sydney NSW 2052 Australia

M

Martina Lessio

School of Chemistry University of New South Wales Sydney NSW 2052 Australia

I

Ichiro Ohnishi

JEOL Ltd. 3‐1‐2 Musashino, Akishima Tokyo 196‐8558 Japan

Z

Zeno R. Ramadhan

Electron Microscope Unit, Mark Wainwright Analytical Centre

D

Dale L. Huber

Center for Integrated Nanotechnologies Sandia National Laboratories Albuquerque NM 87185 USA

L

Liming Dai

ARC Centre of Excellence for Carbon Science and Innovation

W

Wolfgang Schuhmann

Analytical Chemistry – Center For Electrochemical Sciences (CES); Faculty of Chemistry and Biochemistry Ruhr University Bochum, Universitätsstr. 150 Bochum Germany

J

J. Justin Gooding

School of Chemistry

R

Richard D. Tilley

School of Chemistry