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Rationalizing the Influence of the Mn(IV)/Mn(III) Red-Ox Transition on the Electrocatalytic Activity of Manganese Oxides in the Oxygen Reduction Reaction

机译:合理化Mn(IV)/ Mn(III)Red-Ox过渡对氧还原反应中锰氧化物电催化活性的影响

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摘要

Knowledge on the mechanisms of oxygen reduction reaction (ORR) and descriptors linking the catalytic activity to the structural and electronic properties of transition metal oxides enable rational design of more efficient catalysts. In this work ORR electrocatalysis was studied on a set of single and complex Mn (III) oxides with a rotating disc electrode method and cyclic voltammetry. We discovered an exponential increase of the specific electrocatalytic activity with the potential of the surface Mn(IV)/Mn(III) red-ox couple, suggesting the latter as a new descriptor for the ORR electrocatalysis. The observed dependence is rationalized using a simple mean-field kinetic model considering availability of the Mn( III) centers and adsorbate-adsorbate interactions. We demonstrate an unprecedented activity of Mn2O3, ca. 40 times exceeding that of MnOOH and correlate the catalytic activity of Mn oxides to their crystal structure. (C) 2015 Elsevier Ltd. All rights reserved.
机译:关于氧还原反应(ORR)机理的知识以及将催化活性与过渡金属氧化物的结构和电子性质联系起来的描述词可以合理设计更高效的催化剂。在这项工作中,使用转盘电极法和循环伏安法研究了一组单一和复杂的Mn(III)氧化物上的ORR电催化作用。我们发现特定的电催化活性随表面Mn(IV)/ Mn(III)氧化还原对的电势呈指数增加,表明后者是ORR电催化的新描述。考虑到Mn(III)中心的可用性和被吸附物-被吸附物的相互作用,可以使用简单的平均场动力学模型对观察到的依赖性进行合理化处理。我们展示了前所未有的Mn2O3,ca活性。是MnOOH的40倍,并且使Mn氧化物的催化活性与其晶体结构相关。 (C)2015 Elsevier Ltd.保留所有权利。

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