铱
材料科学
质子交换膜燃料电池
催化作用
析氧
纳米颗粒
电化学
多孔性
化学工程
纳米技术
电极
有机化学
复合材料
工程类
化学
物理化学
作者
Marco Faustini,Marion Giraud,Deborah J. Jones,Jacqués Rozière,Marc Dupont,Thomas R. Porter,Sophie Nowak,Mounib Bahri,Ovidiu Ersen,Clément Sánchez,Cédric Boissière,Cédric Tard,Jennifer Péron
标识
DOI:10.1002/aenm.201802136
摘要
Abstract Iridium oxide is the gold‐standard catalyst for the oxygen evolution reaction (OER) in acidic media due to its unmatched activity and stability. Here, a new catalyst architecture comprising a nanoneedle network of iridium‐containing oxides assembled into macroporous micrometric particles with ≈75% of porosity is reported. The rationally designed porous hierarchical structure optimizes the accessibility of reactants and products to the surface of the nanoparticles and maximizes catalyst activity. The materials are easily prepared from aqueous solutions by an industrially viable spray‐drying route through an evaporation self‐assembly mechanism. The versatility of the process enables the preparation of mixed oxides with low iridium content, particles with tunable crystallinity, and various iridium surface species with high electrochemical activity. Highly porous Ir 0.7 Ru 0.3 O 2 outperforms commercial iridium oxide. These materials also represent an ideal platform to assess the reactivity of the iridium and oxygen species involved in the oxygen evolution reaction. Furthermore, it is demonstrated that these highly porous particles are optimal building blocks to be integrated into catalyst layers, without the drawbacks associated with the use of discrete nanoparticles. Fresh‐ and end‐of‐test membrane–electrode assemblies' characterization shows that their particular architecture is preserved upon catalyst layer preparation and after operation in a proton‐exchange membrane electrolysis cell.
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