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Electrospun Ti-Zr Oxide Heterostructures Enable Strongly Anchored Ultralow-Ir Anodes for Durable Acidic Oxygen
Bingzhang Zhang1, Chaochao Dun2, Jiashun Liang1
1Department of Energy, Environmental & Chemical Engineering, Washington University in St. Louis, St. Louis, Missouri 63130, United States.
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Developing ultralow-Ir anode catalysts is desperately needed for proton-exchange-membrane water electrolysis, which requires high activity and adequate stability for the challenging acidic oxygen-evolution reaction. Here, we report a Ti-Zr composite electrospun oxide (ESO) nanorod support that enables high-performance ultralow-Ir anodes. The Zr-containing Ti oxide heterostructures are effective in stabilizing anatase-rich TiO2, tuning the local oxygen-coordination environment, and strengthening the interfacial anchoring of IrOx under acidic anodic conditions. The electrospun porous nanorod network further creates an open, mechanically coherent catalyst layer, thereby improving Ir utilization, ionomer penetration, and mass transport in the ultralow-Ir anode. At a loading of 0.2 mgIr cm-2, the optimized Ir/TiZr20-ESO anode delivers a mass activity of 0.99 A mgIr-1 at 1.45 V, more than 40 times higher than a commercial TiO2-supported IrO2 catalyst. The anode presents compelling performance and durability, achieving 3.0 and 4.0 A cm-2 at 1.75 and 1.83 V, respectively, and sustaining 2000 h of operation at 2.0 A cm-2. Accelerated stress tests up to 525 h over 31,500 cycles also confirm promising long-term durability under dynamic conditions, demonstrating an insignificant decay of 0.4 μV per cycle. Theoretical calculations elucidate that the Ti-Zr oxide heterostructure can suppress Ti demetalation and strengthen IrO2 interfacial binding, rationalizing the improved long-term durability of the ESO-supported ultralow-Ir anode.

