催化作用
介孔材料
电解质
无机化学
过渡金属
活动站点
X射线吸收精细结构
螯合作用
质子交换膜燃料电池
材料科学
金属
膜
化学
光谱学
电极
有机化学
物理化学
量子力学
生物化学
物理
作者
Johanna K. Dombrovskis,Anders E. C. Palmqvist
出处
期刊:Fuel Cells
[Wiley]
日期:2016-01-19
卷期号:16 (1): 23-31
被引量:10
标识
DOI:10.1002/fuce.201500122
摘要
Abstract Transition metal ion‐chelating ordered mesoporous carbons (TM‐OMCs) were studied as polymer electrolyte membrane fuel cell cathode catalysts. The active site structure of the TM‐OMCs was studied by X‐ray absorption spectroscopy in combination with variations of a range of synthesis variables of the TM‐OMCs. The variations were found to have significant influence on the catalyst structure both in the mesoscale and on the atomic local structure allowing for detailed conclusions on the nature of the active sites. The main active site was found to be FeN x chelates. An additional highly active site was found and proposed to be a FeN x ‐dioxygen site. It was further found that the catalytic activity could be increased threefold by acid washing and subsequent heat treatment of the as‐synthesized TM‐OMC materials.
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