Mixed Metal Oxide TiO <sub>2</sub> @RuO <sub>2</sub> Nanostructure over Titanium Substrates as Self-Supporting Electrodes for Oxygen Evolution Reaction
The development of low-cost, efficient, and stable electrodes for electrochemical water splitting remains a serious challenge. Herein, a specific alkaline treatment is used to grow a porous network structure over the surface of the titanium substrates. Afterward, Ru3+ ions are incorporated into the constructed porous network using the SILAR method and an ion exchange process. Loaded Ru3+ ions are subsequently converted into RuO2 using a thermal treatment. During this treatment, there is simultaneous formation of TiO2 and RuO2 which combine to form a TiO2@RuO2 mixed metal oxide nanostructure over the surface of titanium substrates. Resulting self-supporting electrodes (Ti/TiO2@RuO2-x) were characterized using advanced characterization techniques such as XRD, XPS, SEM, EDX, FE-SEM and HR-TEM, and used as counter and working electrodes for OER in an alkaline medium. Electrochemical studies reveal that with low Ru contents of 0.79 ± 0.02 and 2.27 ± 0.09 (at. %) for counter and working respectively, the electron transfer properties, OH– adsorption capacity, and hence, OER activity of the proposed working electrode are significantly enhanced. Moreover, the long-term stability and postcharacterization studies demonstrate the high potential of TiO2 to strongly bind RuO2 at the substrate surface and prevent their dissolution during electrochemical reactions.
Authors
- Vembu Suryanarayanan (ORCID: https://orcid.org/0000-0003-1123-3291)
- Deepak K. Pattanayak (ORCID: https://orcid.org/0000-0003-4438-3421)
- A. G. Kamaha Tchekep
- S. Devaraj
Institutions
- Central Electrochemical Research Institute (IN)
- ElectroHeat (Sweden) (SE)
- Academy of Scientific and Innovative Research (IN)
Publication Details
- Journal
- ACS Applied Energy Materials
- Published
- 2026-03-11
- DOI
- https://doi.org/10.1021/acsaem.5c04021
- Primary Topic
- Electrocatalysts for Energy Conversion
- Type
- article
- Field-Weighted Citation Impact
- 0.00