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Excavated Fe‐N‐C Sites for Enhanced Electrocatalytic Activity in the Oxygen Reduction Reaction
Author(s) -
Jeong Beomgyun,
Shin Dongyoon,
Jeon Hongrae,
Ocon Joey D.,
Mun Bongjin Simon,
Baik Jaeyoon,
Shin HyunJoon,
Lee Jaeyoung
Publication year - 2014
Publication title -
chemsuschem
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.412
H-Index - 157
eISSN - 1864-564X
pISSN - 1864-5631
DOI - 10.1002/cssc.201301374
Subject(s) - electrocatalyst , catalysis , ball mill , materials science , chemical engineering , hydrogen , carbon fibers , carbon nanofiber , inorganic chemistry , x ray photoelectron spectroscopy , noble metal , electrochemistry , chemistry , metallurgy , composite number , organic chemistry , composite material , electrode , engineering
Platinum (Pt) is the best electrocatalyst for the oxygen reduction reaction (ORR) in hydrogen fuel cells, but it is an extremely expensive resource. The successful development of a cost‐effective non‐Pt ORR electrocatalyst will be a breakthrough for the commercialization of hydrogen‐air fuel cells. Ball milling has been used to incorporate metal and nitrogen precursors into micropores of carbon more effectively and in the direct nitrogen‐doping of carbon under highly pressurized nitrogen gas in the process of the preparation of non‐noble ORR catalysts. In this study, we first utilize ball milling to excavate the ORR active sites embedded in Fe‐modified N‐doped carbon nanofibers (Fe‐N‐CNFs) by pulverization. The facile ball‐milling process resulted in a significant enhancement in the ORR activity and the selectivity of the Fe‐N‐CNFs owing to the higher exposure of the metal‐based catalytically active sites. The degree of excavation of the Fe‐based active sites in the Fe‐N‐CNFs for the ORR was investigated with cyclic voltammetry, X‐ray photoelectron spectroscopy, and pore‐size distribution analysis. We believe that this simple approach is useful to improve alternative ORR electrocatalysts up to the level necessary for practical applications.
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