尖晶石
八面体
氧化物
催化作用
超级交换
材料科学
无机化学
结晶学
化学
反铁磁性
晶体结构
凝聚态物理
物理
冶金
生物化学
作者
Ye Zhou,Shengnan Sun,Shibo Xi,Yan Duan,Thirumany Sritharan,Yonghua Du,Zhichuan J. Xu
标识
DOI:10.1002/adma.201705407
摘要
Abstract 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.
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