过电位
析氧
催化作用
溶解
质子交换膜燃料电池
X射线光电子能谱
材料科学
贵金属
无机化学
化学
化学工程
电化学
物理化学
电极
生物化学
工程类
作者
Leopold Lahn,Andrea Maria Mingers,Alan Savan,Alfred Ludwig,Olga Kasian
标识
DOI:10.1002/celc.202300399
摘要
Abstract Anodic oxygen evolution reaction (OER) challenges large scale application of proton exchange membrane water electrolyzers (PEMWE) due to sluggish kinetics, high overpotential and extremely corrosive environment. While Ir oxides currently provide the best balance between activity and stability, the scarcity of Ir and corresponding high market price lead to poor cost‐benefit factors. Mixing Ir with more stable non‐precious Ti reduces the noble metal loading and may implicate stabilization, while addition of more catalytically active Ru ensures a high reaction rate. Here, we examine the activity‐stability behavior of Ru‐Ir‐Ti thin film material libraries with low Ti‐content under the OER conditions. The high sensitivity to the dissolution of the individual alloy components was achieved by using online and off‐line inductively coupled plasma mass spectrometry (ICP‐MS) analysis. Our data reveal that even low Ti additions improve the stability of Ru‐Ir catalysts without sacrificing activity. In particular, 5 at. % of Ti enable stability increase of Ir in the Ru‐Ir catalyst by a factor of 3. Moreover, this catalyst exhibits higher activity compared to the Ti‐free Ru‐Ir alloys with similar Ir content. Observed activity‐stability trends are discussed in light of X‐ray photoelectron spectroscopy data.
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