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Spinel Manganese Ferrites for Oxygen Electrocatalysis: Effect of Mn Valency and Occupation Site

机译:用于氧电相分析的尖晶石锰铁氧体:Mn upency和职业部位的影响

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摘要

Spinel catalysts have been widely explored for the electrochemical oxygen reduction reaction (ORR) and oxygen evolution reaction (OER). To consolidate the understanding on electrocatalysis by spinel family, intermediate spinels should be deliberately examined because most spinel oxides are of intermediate structure. Here, we report an investigation on the ORR and OER performance of intermediate spinel MnFe2O4. The modulation of cation oxidation state and inversion degree of spinel MnFe2O4 were achieved by a simple annealing process. X-ray absorption spectroscopy analysis reveals that the Mn occupancy in octahedral sites varied from 0.25 similar to 0.41 and Mn cations were oxidized from 2+ to 3+ with increasing temperature treatment. Convinced by the leading role of octahedral-geometric, we further reveal the role of Mn oxidation state through normalizing the activity to active Mn-[Oh] site number. Our findings clearly indicate that Mn3+ was more catalytically active than Mn2+ in catalyzing ORR and OER.
机译:已经广泛探索了尖晶石催化剂,用于电化学氧还原反应(ORR)和氧气进化反应(OER)。为了通过尖晶石家族巩固对电常分的理解,应刻意检查中间尖晶石,因为大多数尖晶石氧化物是中间结构。在这里,我们报告了中间尖晶石MNFE2O4的ORR和OER性能的调查。通过简单的退火工艺实现了阳离子氧化状态和尖晶石MNFE2O4的反转度。 X射线吸收光谱分析显示,随着温度的温度处理,八面体位点中的MN占用八点位点的占用率不同于0.41和Mn阳离子。八层面几何的主要作用,我们进一步揭示了通过将活性标准化为活性Mn-λ的位点数来揭示Mn氧化态的作用。我们的研究结果清楚地表明Mn3 +比Mn2 +更催化为催化钻头和oer。

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