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Mn x O y /NC and Co x O y /NC Nanoparticles Embedded in a Nitrogen‐Doped Carbon Matrix for High‐Performance Bifunctional Oxygen Electrodes
Author(s) -
Masa Justus,
Xia Wei,
Sinev Ilya,
Zhao Anqi,
Sun Zhenyu,
Grützke Stefanie,
Weide Philipp,
Muhler Martin,
Schuhmann Wolfgang
Publication year - 2014
Publication title -
angewandte chemie international edition
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.831
H-Index - 550
eISSN - 1521-3773
pISSN - 1433-7851
DOI - 10.1002/anie.201402710
Subject(s) - catalysis , bifunctional , manganese , cobalt , carbon fibers , calcination , nitrogen , inorganic chemistry , oxygen , oxygen evolution , nanoparticle , transition metal , materials science , chemistry , electrocatalyst , electrochemistry , electrode , nanotechnology , biochemistry , organic chemistry , composite number , composite material , metallurgy
Reversible interconversion of water into H 2 and O 2 , and the recombination of H 2 and O 2 to H 2 O thereby harnessing the energy of the reaction provides a completely green cycle for sustainable energy conversion and storage. The realization of this goal is however hampered by the lack of efficient catalysts for water splitting and oxygen reduction. We report exceptionally active bifunctional catalysts for oxygen electrodes comprising Mn 3 O 4 and Co 3 O 4 nanoparticles embedded in nitrogen‐doped carbon, obtained by selective pyrolysis and subsequent mild calcination of manganese and cobalt N 4 macrocyclic complexes. Intimate interaction was observed between the metals and nitrogen suggesting residual M–N x coordination in the catalysts. The catalysts afford remarkably lower reversible overpotentials in KOH (0.1 M ) than those for RuO 2 , IrO 2 , Pt, NiO, Mn 3 O 4 , and Co 3 O 4 , thus placing them among the best non‐precious‐metal catalysts for reversible oxygen electrodes reported to date.