Related Experiment Video
Updated: Jan 13, 2026

Solar-Driven Electrochemical Green Fuel Production from CO2 and Water Using Ti3C2Tx MXene-Supported CuZn and NiCo Catalysts
Published on: November 7, 2025
Ultralow-Iridium Oxygen Evolution Catalyst with Dual-Site Oxide Pathway for Proton Exchange Membrane Water
Xudong Mao1, Mingze Zhu1, Mengke Xie1
1College of Physical Science and Technology & Chemistry Interdisciplinary Research Center, Yangzhou University, Yangzhou 225002, China.
None:
Developing cost-effective low-iridium catalysts for the acidic oxygen evolution reaction (OER) is essential for the advancement of proton exchange membrane (PEM) water electrolyzers. Here, we report a cerium oxide-supported iridium cluster catalyst (Ir@CeO2) that features ultrafine Ir clusters dispersed within a CeO2 matrix, achieving low noble metal loading and favorable activity-stability balance. The Ir@CeO2 exhibits a small overpotential of 197 mV at 10 mA cm-2 and a large mass activity of 247 A gIr-1 at 300 mV, surpassing commercial IrO2 by more than 38 times. The enhanced OER kinetics is attributed to the dual-site oxide pathway mechanism enabled by increased Ir-O covalency and a shortened Ir-Ir distance at chelation interfaces within Ir@CeO2. Utilizing the Ir@CeO2 catalyst in an actual PEM electrolyzer with a minimal Ir loading of 0.3 mg cm-1 demonstrated durable water electrolysis for over 1000 h at a current density of 1 A cm-2 under a cell voltage of 1.68 V.

