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Single-Atom Ruthenium Anchored on Ni4Mo/NiMoO4: Leveraging Metal-Support Interaction for Superior Bifunctional Water
Miaosen Yang1, Chenyuan Li1, Wenkai Xie1
1School of Materials, Shanghai Dianji University, Shanghai, China.
Chemistry (Weinheim an Der Bergstrasse, Germany)
|March 18, 2026
Summary
A novel single-atom ruthenium catalyst (Ru-Ni4Mo/NiMoO4) achieves efficient and stable bifunctional water electrolysis. This advanced catalyst operates at high current densities, paving the way for large-scale green hydrogen production.
Area of Science:
- Catalysis
- Materials Science
- Electrochemistry
Background:
- Industrial-scale green hydrogen production requires efficient and stable bifunctional water electrolysis catalysts.
- Current catalysts struggle to meet demands for high current densities and long-term stability.
Purpose of the Study:
- To develop a novel catalyst for efficient and stable bifunctional water electrolysis.
- To investigate the performance and stability of single-atom ruthenium-anchored catalysts at industrial-scale current densities.
Main Methods:
- Fabrication of a single-atom ruthenium-anchored Ni4Mo/NiMoO4 catalyst using a hydrothermal-annealing coupled reduction strategy.
- Evaluation of bifunctional activity (HER and OER) and stability in alkaline electrolyte at 500 mA cm-2.
- Mechanistic studies to understand the role of single-atom Ru and metal-support interactions (MSI).
Main Results:
- The Ru-Ni4Mo/NiMoO4 catalyst demonstrated low overpotentials of 140 mV (HER) and 420 mV (OER) at 500 mA cm-2.
- Exceptional operational stability exceeding 700 hours at 500 mA cm-2 was achieved.
- Performance surpassed commercial Pt/C and RuO2 catalysts.
Conclusions:
- The single-atom ruthenium catalyst exhibits superior bifunctional activity and stability for water electrolysis.
- Robust MSI and unique needle-like morphology contribute to enhanced catalytic performance and durability.
- This work presents a promising strategy for designing advanced water-splitting catalysts for green hydrogen applications.

