Protonation Enables Durable and Efficient Water Oxidation on Commercial TiO<sub>2</sub>/IrO<sub>2</sub>

The oxygen evolution reaction (OER) performance of commercial TiO<sub>2</sub>-supported IrO<sub>2</sub> (IrO<sub>2</sub>/TiO<sub>2</sub>) suffers from the high electron transfer barriers at the IrO<sub>2</sub>/TiO<sub>2</sub> interface. Herein, we develop a cathodic polarization strategy to protonate TiO<sub>2</sub> (p-TiO<sub>2</sub>) in a commercial IrO<sub>2</sub>/TiO<sub>2</sub> catalyst. The high-density Ti<sup>3+</sup>-OH polaronic states on the surface of protonated TiO<sub>2</sub> greatly contribute to the decrease in the electron transfer barriers at the IrO<sub>2</sub>/TiO<sub>2</sub> interface. As a result, the IrO<sub>2</sub>/p-TiO<sub>2</sub> catalyst exhibits an ultralow overpotential of 246 ± 3 mV at 10 mA/cm<sup>2</sup> and durability over 200 h, attributed to electron compensation from Ti<sup>3+</sup>-OH states suppressing active Ir overoxidation. This electrochemical modification, requiring neither a complex apparatus nor high-temperature processing, establishes a new paradigm for designing high-performance anode catalysts.

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Publication Details

Journal
The Journal of Physical Chemistry Letters
Published
2025-09-10
DOI
https://doi.org/10.1021/acs.jpclett.5c02227
Citations
1
Primary Topic
Electrocatalysts for Energy Conversion
Type
article
Field-Weighted Citation Impact
0.36
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article

Protonation Enables Durable and Efficient Water Oxidation on Commercial TiO2/IrO2

Shicheng Yan, Zhigang Zou, Da Wei Huang, Hongqiao Hu et al.
1 citations
The Journal of Physical Chemistry Letters
Electrocatalysts for Energy Conversion
0.36
article

Protonation Enables Durable and Efficient Water Oxidation on Commercial TiO2/IrO2

Shicheng Yan, Zhigang Zou, Da Wei Huang, Hongqiao Hu, Yu Du
article en
1 citations

Abstract

The oxygen evolution reaction (OER) performance of commercial TiO<sub>2</sub>-supported IrO<sub>2</sub> (IrO<sub>2</sub>/TiO<sub>2</sub>) suffers from the high electron transfer barriers at the IrO<sub>2</sub>/TiO<sub>2</sub> interface. Herein, we develop a cathodic polarization strategy to protonate TiO<sub>2</sub> (p-TiO<sub>2</sub>) in a commercial IrO<sub>2</sub>/TiO<sub>2</sub> catalyst. The high-density Ti<sup>3+</sup>-OH polaronic states on the surface of protonated TiO<sub>2</sub> greatly contribute to the decrease in the electron transfer barriers at the IrO<sub>2</sub>/TiO<sub>2</sub> interface. As a result, the IrO<sub>2</sub>/p-TiO<sub>2</sub> catalyst exhibits an ultralow overpotential of 246 ± 3 mV at 10 mA/cm<sup>2</sup> and durability over 200 h, attributed to electron compensation from Ti<sup>3+</sup>-OH states suppressing active Ir overoxidation. This electrochemical modification, requiring neither a complex apparatus nor high-temperature processing, establishes a new paradigm for designing high-performance anode catalysts.

The Journal of Physical Chemistry LettersVol. 16(37)
Collaborative Innovation Center of Advanced Microstructures (CN), Nanjing University (CN)
Openalex Percentile: Top 39%
Electrocatalysts for Energy Conversion
0.36
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