Affiliation:
1. State Key Laboratory of Inorganic Synthesis and Preparative Chemistry, College of Chemistry Jilin University Changchun 130012 China
2. Key Laboratory of Automobile Materials of MOE School of Materials Science and Engineering Jilin University Changchun 130012 China
3. Department of Mechanical and Mechatronics Engineering Waterloo Institute for Nanotechnology University of Waterloo Waterloo Ontario N2L 3G1 Canada
Abstract
AbstractThe design of a low‐iridium‐loading anode catalyst layer with high activity and durability is a key challenge for a proton exchange membrane water electrolyzer (PEMWE). Here, the synthesis of a novel supported IrO2 nanocatalyst with a tri‐layered structure, dubbed IrO2@TaOx@TaB that is composed of ultrasmall IrO2 nanoparticles anchored on amorphous TaOx overlayer of TaB nanorods is reported. The composite electrocatalyst shows great activity and stability toward the oxygen evolution reaction (OER) in acid, thanks to its dual‐interface structural feature. The electronic interaction in IrO2/TaOx interface can regulate the coverage of surface hydroxyl groups, the Ir3+/ Ir4+ ratio, and the redox peak potential of IrO2 for enhancing OER activity, while the dense TaOx overlayer can prevent further oxidation of TaB substrate and stabilize the IrO2 catalytic layers for improving structural stability during OER. The IrO2@TaOx@TaB can be used to fabricate an anode catalyst layer of PEMWE with an iridium‐loading as low as 0.26 mg cm−2. The low‐iridium‐loading PEMWE delivers high current densities at low cell voltages (e.g., 3.9 A cm−2@2.0 V), and gives excellent activity retention for more than 1500 h at 2.0 A cm−2 current density.
Funder
National Key Research and Development Program of China
National Natural Science Foundation of China
Fundamental Research Funds for the Central Universities
Cited by
1 articles.
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