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Nanostructured IrO supported on N-doped TiO2 as an efficient electrocatalyst towards acidic oxygen evolution reaction
Guoqiang Li1, Hongrui Jia1, Huan Liu2
1College of Energy Storage Technology, Shandong University of Science and Technology Qingdao 266590 China ligq@sdust.edu.cn.
This study introduces N-doped TiO2 as a support for Iridium Oxide (IrO2) nanoparticles, significantly reducing Iridium use in oxygen evolution reactions for water electrolysis. The new catalyst shows enhanced activity and stability, paving the way for more efficient green hydrogen production.
Area of Science:
- Materials Science
- Electrochemistry
- Catalysis
Background:
- The development of efficient and cost-effective electrocatalysts is crucial for advancing solid polymer electrolyte water electrolysis (SPEWE).
- Iridium (Ir) based catalysts are highly effective for the oxygen evolution reaction (OER) but their high cost and scarcity limit widespread application.
- Reducing Iridium loading without sacrificing performance is a key challenge in developing sustainable SPEWE systems.
Purpose of the Study:
- To develop a novel electrocatalyst for the oxygen evolution reaction (OER) that minimizes Iridium (Ir) consumption.
- To enhance the catalytic activity, electrical conductivity, and stability of Ir-based catalysts using a modified support material.
- To investigate the potential of nitrogen-doped titanium dioxide (N-TiO2) as a support for IrO2 nanoparticles in acidic OER applications.
Main Methods:
- Nitrogen (N) doping of titanium dioxide (TiO2) was achieved through facile ammonia (NH3) gas treatment.
- Iridium oxide (IrO2) nanoparticles were synthesized and supported on the N-doped TiO2 (N-TiO2) material.
- Electrocatalytic performance for OER was evaluated in acidic media, focusing on overpotential, mass activity, and long-term stability.
- Single cell electrolysis tests were conducted to assess the practical performance of the developed catalyst.
Main Results:
- The N-doping of TiO2 significantly improved its electrical conductivity and the dispersion/anchoring of IrO2 nanoparticles.
- The resulting IrO2/N-TiO2 electrocatalyst demonstrated excellent catalyst utilization, activity, and stability for the OER.
- An overpotential of only 270 mV was required to achieve 10 mA cm-2, with a mass activity of 278.7 A gIr-1 at 1.55 VRHE.
- In a single cell, the IrO2/N-TiO2 anode catalyst resulted in a lower cell voltage (1.761 V at 2.0 A cm-2) compared to commercial IrO2.
Conclusions:
- Nitrogen doping of TiO2 is an effective strategy to enhance the performance of IrO2 catalysts for acidic OER.
- The IrO2/N-TiO2 electrocatalyst offers a promising pathway to reduce Iridium loading while maintaining high catalytic efficiency and durability.
- This advancement contributes to the cost-effective development of solid polymer electrolyte water electrolysis systems for sustainable energy.
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