煅烧
氧化物
X射线光电子能谱
循环伏安法
材料科学
铱
无定形固体
催化作用
基质(水族馆)
扫描电子显微镜
析氧
化学工程
无机化学
结晶度
化学
电化学
结晶学
物理化学
冶金
有机化学
电极
工程类
海洋学
复合材料
地质学
作者
Tobias Reier,D. Teschner,Thomas Lunkenbein,Arno Bergmann,Sören Selve,Ralph Kraehnert,R. Schlögl,Peter Strasser
摘要
The morphology, crystallinity, and chemical state of well-defined Ir oxide nanoscale thin-film catalysts prepared on Ti substrates at various calcination temperatures were investigated. Special emphasis was placed on the calcination temperature-dependent interaction between Ir oxide film and Ti substrate and its impact on the electrocatalytic oxygen evolution reaction (OER) activity. The Ir oxide films were characterized by scanning electron microscopy, transmission electron microscopy, scanning transmission electron microscopy, energy dispersive X-ray spectroscopy, X-ray diffraction, X-ray photoelectron spectroscopy and cyclic voltammetry. Furthermore, temperature programmed reduction was applied to study the Ir oxide species formed as a function of calcination temperature and its interaction with the Ti substrate. A previously unachieved correlation between the electrocatalytic OER activity and the nature and structural properties of the Ir oxide film was established. We find that the crystalline high temperature Ir oxide species is detrimental, whereas low temperature amorphous Ir oxy-hydroxides are highly active and efficient catalysts for the OER. Moreover, at the highest applied calcination temperature (550°C), Ti oxides, originating from the substrate, strongly affect chemical state and electrocatalytic OER activity of the Ir oxide film.
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