Highly active electrocatalyst for oxygen reduction reaction from pyrolyzing carbon-supported iron tetraethylenepentamine complex

被引:14
作者
Zhang, Hui-Juan [1 ]
Li, Haoliang [1 ]
Li, Xiangtai [1 ]
Zheng, Shiyou [1 ]
Zhao, Bin [1 ]
Yang, Junhe [1 ]
机构
[1] Shanghai Univ Sci & Technol, Sch Mat Sci & Engn, Shanghai 200093, Peoples R China
基金
美国国家科学基金会;
关键词
Oxygen reduction reaction; Non-precious metal catalyst; Iron; Tetraethylenepentamine; Nitrogen-doped; ELECTROLYTE FUEL-CELLS; METAL-FREE ELECTROCATALYSTS; NANOTUBE ARRAYS; ALKALINE MEDIA; CATALYSTS; NITROGEN; CO; GRAPHENE; COBALT; FE;
D O I
10.1016/j.apcatb.2014.06.014
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Development of non-precious metal catalysts for oxygen reduction reaction (ORR) is of great importance due to their significant potential application in energy converting and storing devices. In this work, a class of non-precious metal catalyst is prepared by using a simple and low-cost N-5 structure tetraethylenepentamine ligand, i.e. pyrolyzing iron tetraethylenepentamine chelate on carbon (FeTEPA/C) at 800 degrees C. The FeTEPA/C catalyst is characterized by transmission electron microscopy, Raman, X-ray diffraction, elemental analysis and X-ray photoelectron spectroscopy. It has been found that the unique FeTEPA/C catalyst contains 1.48 at% nitrogen and the absence of Fe-containing aggregates, and shows a higher catalytic activity towards the ORR than the commercial Pt/C catalyst either in acid or in alkaline electrolyte. Furthermore, a better ORR catalytic activity in terms of onset potential, peak potential, half-wave potential and limited-diffusing current is displayed in alkaline medium. The ORR on the FeTEPA/C catalyst follows a four-electron pathway among all the studied potential. The above superiorities make it a promising candidate for substituting the commercial Pt/C catalyst. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:676 / 683
页数:8
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