Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
6602407 | Electrochimica Acta | 2018 | 26 Pages |
Abstract
Iron-nitrogen-carbon materials (Fe-N-C) are considered as one of the most promising none precious candidates for oxygen reduction reaction. However, the role of iron carbides, one of the important accompanied species in Fe-N-C catalyst for oxygen reduction reaction, remains controversial. Herein, two different types of 3D graphene-based Fe-N-C catalysts with exposed and encapsulated Fe carbides were synthesized via pyrolysis of self-polymerization compounds of 2,6-Diaminopyridine using Fe(OH)3 and FeCl3 as both initiators and Fe sources, respectively. Interestingly, Mössbauer spectroscopy and X-ray photoelectron spectroscopy measurements show that both catalysts are composed of same Fe species with FeIIN4/C, iron carbide, iron nitride, metallic iron where the proportion of each corresponding component is similar. However, there is a big gap between the two catalysts in catalytic performance for oxygen reduction reaction. The kinetic current densities of the former catalyst (3.565â¯mAâ¯cmâ2) at 0.9â¯V vs.RHE is 4.68 times and 1.50 times higher than that of the latter (0.7617â¯mAâ¯cmâ2) and Pt/C catalyst (2.376â¯mAâ¯cmâ2), respectively. This sharp contrast directly identifies the critical role of exposed Fe carbides nanodots on Fe-N-C in promoting Fe-N-C activity for oxygen reduction reaction. The new discovery brings a new insight into developing advanced none precious metal catalysts.
Keywords
Related Topics
Physical Sciences and Engineering
Chemical Engineering
Chemical Engineering (General)
Authors
Xiaoran Zhang, Dandan Lyu, Yaser Bahari Mollamahale, Feng Yu, Ming Qing, Shibin Yin, Xinyi Zhang, Zhi Qun Tian, Pei Kang Shen,