催化作用
电催化剂
X射线光电子能谱
循环伏安法
电化学
金属有机骨架
傅里叶变换红外光谱
电解质
氧化还原
化学
无机化学
金属
化学工程
材料科学
电极
物理化学
有机化学
工程类
吸附
作者
Zheng‐Hong Huang,Nanhong Xie,Min Zhang,Bo‐Qing Xu
出处
期刊:Chemsuschem
[Wiley]
日期:2018-10-19
卷期号:12 (1): 200-207
被引量:32
标识
DOI:10.1002/cssc.201801886
摘要
Pyrolyzed base-metal-based metal-organic frameworks (MOFs) with FeNx coordination are emerging as nonprecious metal catalysts for electrochemical oxygen reduction reaction (ORR). However, surprisingly, nonpyrolyzed MOFs involving Fe-N coordination have not been explored for the ORR. This study concerns the catalytic performance of a semiconducting nonpyrolyzed iron triazolate framework (FeTa2 ) for ORR in alkaline electrolyte. The FeTa2 catalyst is studied as composites with different amounts of conductive Ketjenblack carbon (KB). The performance of these FeTa2 -x KB (x denotes the KB/FeTa2 weight ratio) composites by onset and half-wave potentials of ORR appears to be superior to most previously documented nonpyrolyzed MOFs. Characterization by elemental analysis, FTIR spectroscopy, XPS, and cyclic voltammetry suggest that N-FeIII -OH- sites at the surface of FeTa2 function as the catalytic active sites. This FeTa2 also shows very stable activity during ORR, as supported by accelerated durability test of the FeTa2 -x KB sample (20 000 cycles, ca. 90 h). The framework structure of FeTa2 remains intact during the durability test, which would help to explain its excellent catalytic durability. This would be the first study demonstrating efficient and stable ORR catalysis by a nonpyrolyzed Fe-N coordination-based MOF material.
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