Semi-metallic hydroxide supported single-atom catalysts for sustainable water oxidation
Developing efficient electrocatalysts towards water oxidation is of critical importance for numerous environmental and energy technologies. Single-atom catalysts have been widely recognized as a promising route, they are however often anchored on semiconducting substrates such as hydroxides, which inherently limits the electrical conductivity and overall catalytic efficiency. In this work, single-atom Ru catalysts are immobilized on a semi-metallic layered double hydroxide substrate (Ru-SM LDH) to achieve highly efficient water oxidation. The as-designed Ru-SM LDH catalyst displayed an overpotential of 270 mV to deliver an oxygen evolution reaction (OER) current density of 100 mA cm<sup>−2</sup>, which was 60 mV lower than that of commercial RuO<sub>2</sub>. <i>In-situ</i> electrochemical impedance spectroscopy revealed that Ru-SM LDH exhibited a reduced solution resistance and diminished charge transfer resistance during catalysis, leading to the enhanced OER performance. An electrolyzer assembled with Ru-SM LDH anode and commercial Ni mesh cathode achieved a water electrolysis current density of 400 mA cm<sup>−2</sup> at 1.65 V and demonstrated exceptional stability for 1000 h, surpassing that of Ni||Ni electrolyzer (1.92 V, 350 h). These findings established the design of single-atom catalysts supported on semi-metallic hydroxide substrates as a robust pathway toward efficient water electrolysis catalysts.
Authors
- Bo Han (ORCID: https://orcid.org/0009-0002-8801-4038)
- Xiaoqing Ma (ORCID: https://orcid.org/0009-0006-1550-6436)
- Zhiwen Cao
- Yuzhe Cao
- Zhao Cai
- Zunhua Ke
Institutions
- China University of Geosciences (CN)
- Shenzhen Research Institute of China University of Geosciences (CN)
- Huainan Mining Industry Group (China) (CN)
Publication Details
- Journal
- Environmental chemistry and safety
- Published
- 2026-05-01
- DOI
- https://doi.org/10.26599/ecs.2026.9600029
- Primary Topic
- Electrocatalysts for Energy Conversion
- Type
- article
- Field-Weighted Citation Impact
- 0.00