Highly Active and Durable Iridium Nickel Oxide Catalyst for a Proton Exchange Membrane Water Electrolyzer with Low Iridium Loading
作者
Hyeseong Jeon,Sun Seo Jeon,Sung June Cho,Hyunjoo Lee
出处
期刊:Meeting abstracts [Institute of Physics] 日期:2026-07-07卷期号:MA2026-01 (36): 1719-1719
标识
DOI:10.1149/ma2026-01361719mtgabs
摘要
Minimizing iridium (Ir) usage is critical for the commercialization of proton exchange membrane water electrolyzer (PEMWE). Herein, layered monoclinic iridium nickel oxide (IrNiO x ) platelets were synthesized via a molten salt method and investigated as oxygen evolution reaction (OER) catalysts in a PEMWE. The IrNiO x hexagonal platelets feature an edge-sharing octahedral framework, in which Ni atoms partially substitute for Ir sites in the crystalline lattice. Layered monoclinic IrNiO x catalyst exhibits high OER activity while effectively suppressing Ni dissolution from the bulk lattice in acidic environments. In a membrane-electrode-assembly (MEA) condition, the unique morphology of these hexagonal platelets enhances interconnectivity within the catalyst layer, thereby promoting efficient electron transfer. Even at a low Ir loading of 0.2 mg Ir cm -2 , the platelets achieved a high performance of 1.70 V at 1 A cm -2 . Furthermore, the PEMWE exhibited stable operation for 150 h with a Ti porous transport layer (PTL) without Pt coating, outperforming commercial Ir oxide and rutile IrO 2 . When Pt-coated Ti PTL was used, the PEMWE was operated stably for 500 h. These results confirm that incorporating earth-abundant transition metals into the Ir oxide lattice is a promising strategy for reducing iridium loading in high performance PEMWEs.