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Superexchange Effects on Oxygen Reduction Activity of Edge‐Sharing [Co x Mn 1− x O 6 ] Octahedra in Spinel Oxide
Author(s) -
Zhou Ye,
Sun Shengnan,
Xi Shibo,
Duan Yan,
Sritharan Thirumany,
Du Yonghua,
Xu Zhichuan J.
Publication year - 2018
Publication title -
advanced materials
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 10.707
H-Index - 527
eISSN - 1521-4095
pISSN - 0935-9648
DOI - 10.1002/adma.201705407
Subject(s) - spinel , octahedron , oxide , superexchange , catalysis , materials science , inorganic chemistry , crystallography , chemistry , antiferromagnetism , condensed matter physics , crystal structure , physics , metallurgy , biochemistry
Mn–Co containing spinel oxides are promising, low‐cost electrocatalysts for the oxygen reduction reaction (ORR). Most studies are devoted to the design of porous Mn–Co spinels or to strongly coupled hybrids (e.g., MnCo 2 O 4 /N‐doped‐rmGO) to maximize the mass efficiency. The lack of analyses by metal oxide intrinsic activity (activity normalized to catalysts' surface area) hinders the development of fundamental understanding of the physicochemical principles behind the catalytic activities. A systematic study on the composition dependence of ORR in ZnCo x Mn 2− x O 4 ( x = 0.0–2.0) spinel is presented here with special attention to the role of edge sharing [Co x Mn 1− x O 6 ] octahedra in the spinel structure. The ORR specific activity of ZnCo x Mn 2− x O 4 spans across a potential window of 200 mV, indicating an activity difference of ≈3 orders of magnitude. The curve of composition‐dependent ORR specific activity as a function of Co substitution exhibits a volcano shape with an optimum Mn/Co ratio of 0.43. It is revealed that the modulated e g occupancy of active Mn cations (0.3–0.9), as a consequence of the superexchange effect between edge sharing [CoO 6 ] and [MnO 6 ], reflects the ORR activity of edge sharing [Co x Mn 1− x O 6 ] octahedra in the ZnCo x Mn 2− x O 4 spinel oxide. These findings offer crucial insights in designing spinel oxide catalysts with fine‐tuned e g occupancy for efficient catalysis.