Graphene-supported non-precious metal electrocatalysts for oxygen reduction reactions: the active center and catalytic mechanism

被引:17
|
作者
Li, Baosheng [1 ,2 ]
Zhang, Lili [4 ]
Chen, Luwei [4 ]
Cai, Xiaoyi [3 ]
Lai, Linfei [1 ,2 ]
Wang, Zhan [4 ]
Shen, Zexiang [3 ]
Lin, Jianyi [3 ]
机构
[1] Nanjing Tech Univ NanjingTech, KLOFE, 30 South Puzhu Rd, Nanjing 211816, Jiangsu, Peoples R China
[2] Nanjing Tech Univ NanjingTech, Jiangsu Natl Synergist Innovat Ctr Adv Mat SICAM, IAM, 30 South Puzhu Rd, Nanjing 211816, Jiangsu, Peoples R China
[3] Nanyang Technol Univ, Energy Res Inst NTU ERIAN, 1 CleanTech Loop,06-04,CleanTech One, Singapore 637141, Singapore
[4] ASTAR, Inst Chem & Engn Sci, 1 Pesek Rd, Jurong Isl 62783, Singapore
关键词
NITROGEN-CONTAINING CARBON; FUEL-CELLS; ELECTRONIC-STRUCTURE; PHOTOELECTRON-SPECTROSCOPY; IRON; FILMS; CO; STABILITY; ALLOYS; COBALT;
D O I
10.1039/c6ta00555a
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
In this work, non-precious metal catalysts (FeCoN) were loaded onto the surface of N-modified graphene (N-G), graphite and activated carbon during a simple yet effective chemical process. The oxygen reduction reaction (ORR) performance of the as-prepared catalysts with different pyrolysis temperatures were evaluated in 0.5 M H2SO4. The use of N-G at a pyrolysis temperature of 750 degrees C yielded the highest catalyst activity, while both the metal nitrides (MeN) and pyridinic N were demonstrated as the active center for the ORR. The pyridinic-N, which sits surrounding MeN works synergistically with metal nitrides to enhance the catalytic activity of the MeN/ N-G composite. A maximum power density output of 130 mWcm(-2) at 0.25 V was achieved in a membrane electrode assembly (MEA) using FeCoN-N-G as a cathode catalyst. The mechanism of the ORR at the catalyst and the nature of the active center are discussed.
引用
收藏
页码:7148 / 7154
页数:7
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