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Herein, ionomer-free amorphous iridium oxide (IrO) thin electrodes are first developed as highly active anodes for proton exchange membrane electrolyzer cells (PEMECs) via low-cost, environmentally friendly, and easily scalable electrodeposition at room temperature. Combined with a Nafion 117 membrane, the IrO-integrated electrode with an ultralow loading of 0.075 mg cm delivers a high cell efficiency of about 90%, achieving more than 96% catalyst savings and 42-fold higher catalyst utilization compared to commercial catalyst-coated membrane (2 mg cm). Additionally, the IrO electrode demonstrates superior performance, higher catalyst utilization and significantly simplified fabrication with easy scalability compared with the most previously reported anodes. Notably, the remarkable performance could be mainly due to the amorphous phase property, sufficient Ir content, and rich surface hydroxide groups in catalysts. Overall, due to the high activity, high cell efficiency, an economical, greatly simplified and easily scalable fabrication process, and ultrahigh material utilization, the IrO electrode shows great potential to be applied in industry and accelerates the commercialization of PEMECs and renewable energy evolution.
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http://dx.doi.org/10.1007/s40820-024-01411-7 | DOI Listing |
Nat Commun
September 2025
State Key Laboratory of Inorganic Synthesis and Preparative Chemistry, College of Chemistry, Jilin University, Changchun, China.
The dynamic reconstruction of oxygen evolution electrocatalysts dictates their performance, yet conventional Ir-based materials face an inherent activity-stability trade-off due to surface amorphization into hydrous IrO phases accompanied by lattice oxygen mechanisms. Here, we uncover a distinct reconstruction pathway for supported Ir nanoparticles, where a TiO@Ti substrate drives a bulk phase transition from metallic Ir to crystalline rutile IrO during electrocatalysis. Unlike surface-limited amorphization, this support-guided crystallization shifts the reaction mechanism from involving lattice oxygen mechanism to the complete adsorbate evolution mechanism, as confirmed by mechanistic and structural analyses.
View Article and Find Full Text PDFJ Am Chem Soc
August 2025
Graduate School of Human and Environmental Studies, Kyoto University, Yoshida Nihonmatsu Cho, Sakyo, Kyoto 606-8501, Japan.
Iridium oxide is a benchmark catalyst for anodic oxygen evolution reactions due to its high activity and durability. However, debates persist regarding the short lifespan of reaction intermediates and whether amorphous phases exhibit higher activity in comparison to crystalline ones. Herein, we examined IrO catalysts with different degrees of crystallinity (SA3.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
July 2025
Department of Energy, Environmental, and Chemical Engineering, Washington University in St. Louis, St. Louis, MO, 63130, USA.
The current high Ir loading (∼2 mg cm) in proton exchange membrane water electrolyzers (PEMWEs) severely hinders their applications for green hydrogen production. Reducing Ir loading while maintaining high performance and durability for the oxygen evolution reaction (OER) anode is critical for the Gigawatt-scale deployment of PEMWEs. Herein, we report an ultra-low Ir anode, consisting of Re-doped Ir nanoparticles anchored on Pt nanowire networks, enabling rational catalyst design at the atomic scale and electrode structure engineering at the nanoscale.
View Article and Find Full Text PDFNanomicro Lett
July 2025
Center of Hydrogen Science, School of Materials Science and Engineering, Shanghai Jiao Tong University, Shanghai, 2000240, People's Republic of China.
The development of highly efficient and durable bifunctional catalysts with minimal precious metal usage is critical for advancing proton exchange membrane water electrolysis (PEMWE). We present an iridium-platinum nanoalloy (IrPt) supported on lanthanum and nickel co-doped cobalt oxide, featuring a core-shell architecture with an amorphous IrPtOx shell and an IrPt core. This catalyst exhibits exceptional bifunctional activity for oxygen and hydrogen evolution reactions in acidic media, achieving 2 A cm at 1.
View Article and Find Full Text PDFJ Biomed Mater Res A
July 2025
Department of Chemical Engineering, McGill University, Quebec, Canada.
Implantable neural prosthetics with stimulating electrodes are increasingly employed in medical practices to treat neural disabilities. The electrode material is expected to provide high charge storage and injection capacity (CSC/CIC) and low impedance for safe, efficient, and precise neural stimulation, while at the same time, being small. To improve the current state-of-the-art neural-electrode material, iridium oxide (IrOx), IrBiOx coatings of various compositions (m = 0, 0.
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