Zirconium Oxynitride-Catalyzed Oxygen Reduction Reaction at Polymer Electrolyte Fuel Cell Cathodes
Author(s) -
Mitsuharu Chisaka,
Akimitsu Ishihara,
Hiroyuki Morioka,
Takaaki Nagai,
Shihong Yin,
Yoshiro Ohgi,
Koichi Matsuzawa,
Shigenori Mitsushima,
Kenichiro Ota
Publication year - 2017
Publication title -
acs omega
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.779
H-Index - 40
ISSN - 2470-1343
DOI - 10.1021/acsomega.6b00555
Subject(s) - oxygen reduction reaction , electrolyte , zirconium , catalysis , oxygen , cathode , materials science , fuel cells , reduction (mathematics) , inorganic chemistry , oxygen reduction , chemical engineering , chemistry , organic chemistry , electrochemistry , electrode , engineering , geometry , mathematics
Most nonplatinum group metal (non-PGM) catalysts for polymer electrolyte fuel cell cathodes have so far been limited to iron(cobalt)/nitrogen/carbon [Fe(Co)/N/C] composites owing to their high activity in both half-cell and single-cell cathode processes. Group IV and V metal oxides, another class of non-PGM catalysts, are stable in acidic media; however, their activities have been mostly evaluated for half-cells, with no single-cell performances comparable to those of Fe/N/C composites reported to date. Herein, we report successful syntheses of zirconium oxynitride catalysts on multiwalled carbon nanotubes, which show the highest oxygen reduction reaction activity among oxide-based catalysts. The single-cell performance of these catalysts reached 10 mA cm -2 at 0.9 V, being comparable to that of state-of-the-art Fe/N/C catalysts. This new record opens up a new pathway for reaching the year 2020 target set by the U.S. Department of Energy, that is, 44 mA cm -2 at 0.9 V.
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