Wet chemical synthesis of nitrogen-doped graphene towards oxygen reduction electrocatalysts without high-temperateure pyrolysis

被引:259
作者
Zhang, Yuanjian [1 ]
Fugane, Keisuke [1 ]
Mori, Toshiyuki [1 ]
Niu, Li [2 ]
Ye, Jinhua [1 ]
机构
[1] Natl Inst Mat Sci, Environm Remediat Mat Unit, Int Ctr Mat Nanoarchitecton MANA, Int Ctr Young Scientists ICYS,Battery Mat Unit, Tsukuba, Ibaraki 3050044, Japan
[2] Chinese Acad Sci, Changchun Inst Appl Chem, Engn Lab Modern Analyt Tech, State Key Lab Electroanalyt Chem, Changchun 130022, Peoples R China
基金
日本学术振兴会;
关键词
METAL-FREE ELECTROCATALYSTS; FUEL-CELLS; O-2; REDUCTION; CATALYSTS; CARBON; OXIDE; IRON; ELECTROREDUCTION; GRAPHITE; COBALT;
D O I
10.1039/c2jm00044j
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
The oxygen reduction reaction (ORR) is one of the important reactions not only in life processes but also in artificial energy conversion systems, such as fuel cells and metal/air batteries. As one of the non-precious ORR catalysts, N-doped carbon materials show an exciting activity, but most of them were universally synthesized by high-temperature pyrolysis or annealing up to 1100 degrees C in the past few decades, which makes the structural manipulation of the catalysts extremely difficult. Here, we propose that ORR active N-doped carbon catalysts could, in principle, be prepared via a sophisticated wet chemical reaction between a reactive graphitic carbon template (e.g. graphene oxide) and N-containing molecules (e.g. dicyandiamide) at temperatures as low as 180 degrees C. Without any high-temperature treatments, for example, the as-prepared N-doped reduced graphene oxide with additional Fe-containing nanoparticles showed an impressive ORR catalytic activity that was comparable to many previous N-doped carbon from high-temperature pyrolysis. Rational utilization of the graphitic carbon template, the N-containing molecules, and the wet chemical reactions may offer a low-temperature route to create interesting ORR electrocatalysts with easier surface properties manipulation.
引用
收藏
页码:6575 / 6580
页数:6
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