IrW nanochannel support enabling ultrastable electrocatalytic oxygen evolution at 2 A cm−2 in acidic media
Rui Li, Haiyun Wang, Fei Hu, K.C. Chan, Xiongjun Liu, Zhaoping Lü, Jing Wang, Zhibin Li, Longjiao Zeng, Yuanyuan Li, Xiaojun Wu, Yujie Xiong
Abstract
Abstract A grand challenge for proton exchange membrane electrolyzers is the rational design of oxygen evolution reaction electrocatalysts to balance activity and stability. Here, we report a support-stabilized catalyst, the activated ~200 nm-depth IrW nanochannel that achieves the current density of 2 A cm −2 at an overpotential of only ~497 mV and maintains ultrastable gas evolution at 100 mA cm −2 at least 800 h with a negligible degradation rate of ~4 μV h −1 . Structure analyses combined with theoretical calculations indicate that the IrW support alters the charge distribution of surface (IrO 2 ) n clusters and effectively confines the cluster size within 4 (n≤4). Such support-stabilizing effect prevents the surface Ir from agglomeration and retains a thin layer of electrocatalytically active IrO 2 clusters on surface, realizing a win-win strategy for ultrahigh OER activity and stability. This work would open up an opportunity for engineering suitable catalysts for robust proton exchange membrane-based electrolyzers.