57Fe-Mossbauer spectroscopy and electrochemical activities of graphitic layer encapsulated iron electrocatalysts for the oxygen reduction reaction

被引:50
作者
Zhong, Lijie [1 ]
Frandsen, Cathrine [2 ]
Morup, Steen [2 ]
Hu, Yang [1 ]
Pan, Chao [1 ]
Cleemann, Lars Nilausen [1 ]
Jensen, Jens Oluf [1 ]
Li, Qingfeng [1 ]
机构
[1] Tech Univ Denmark, Dept Energy Convers & Storage, Kemitorvet 207, DK-2800 Lyngby, Denmark
[2] Tech Univ Denmark, Dept Phys, Bldg 307, DK-2800 Lyngby, Denmark
关键词
Fe-57-Mossbauer spectroscopy; Encapsulated Fe catalysts; Oxygen reduction reaction; Fuel cells; NITROGEN-DOPED CARBON; PEM FUEL-CELLS; FE/N/C-CATALYSTS; NANOPARTICLES; SITES; ORR; IDENTIFICATION; NANOTUBES; GRAPHENE; CARBIDE;
D O I
10.1016/j.apcatb.2017.09.014
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
Graphitic layer encapsulated iron based nanoparticles (G@FeNPs) have recently been disclosed as an interesting type of highly active electrocatalysts for the oxygen reduction reaction (ORR). However, the complex composition of the metal-containing components and their contributions in catalysis remain unclear. As a representative catalyst of the unique encapsulated structure, a series of G@FeNPs catalysts were prepared by a high-pressure pyrolytic process with uniform and essentially identical morphologies but varied compositions. The catalysts exhibited a high onset potential of 0.85 V at 0.1 mA cm(-2) in acidic media. By Fe-57-Mossbauer spectroscopy the iron containing components were identified including alpha-Fe, gamma-Fe, gamma-Fe2O3, and Fe3C as well as a minor doublet component due to Fe3+ in high spin and/or Fe2+ in low spin state. The ORR activities are evaluated in terms of the mass specific kinetic current density found to be positively correlated with the Fe3C content in the range of study, indicating involvement of the encapsulated nanoparticles in the ORR catalysis. The recognition of the Fe compositions and active sites provides new insights to the confined Fe-based ORR electrocatalysts and therefore options for further development of non-precious metal materials.
引用
收藏
页码:406 / 412
页数:7
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