Ir Catalyst on High-Electron-Density Support

56× mass activity

Electrons transferred from Cu-TiO2 support to Ir nanoparticles suppress Ir oxidation and stabilize active oxygen species, dramatically enhancing OER activity and stability.

Haoran, Jiang · Zichen, Wang · Zhirang, Liu · Wei, Qu · Jianan, Chen · Lv, Haifeng · Zhong, Jun · Cheng, Niancai

Applied Catalysis B: Environmental 2027

Specifications

Mass activity
{'zh': '5.38', 'en': '5.38'} A mgIr⁻¹
Current density (PEMWE)
{'zh': '3.0', 'en': '3.0'} A cm⁻²
Stable operation time
{'zh': '1000', 'en': '1000'} h
Durability (PEMWE)
{'zh': '600', 'en': '600'} h

Advantages

56× mass activity

Electron transfer from Cu-TiO2 to Ir creates an electron-rich state, stabilizing adsorbed O species, modulating intermediate adsorption and lowering the O*-OOH* energy barrier, thereby greatly accelerating OER kinetics.

Stable over 1000 h

The electronic effect suppresses Ir oxidation during OER, stabilizing Oads-Ir species, enabling long-term activity retention.

High PEMWE performance

In a real membrane electrode, a low Ir loading of 0.3 mgIr cm⁻² achieves 3.0 A cm⁻² at 1.879 V (80 °C) with 600 h durability at 1.0 A cm⁻².

Applications