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Mechanistic study on the activity of manganese oxide catalysts for oxygen reduction reaction in an aprotic electrolyte

机译:非质子电解质中锰氧化物催化剂的氧还原反应活性机理研究

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Despite a large effort in catalyst research over the past decade, the benefit of electrocatalysts for the oxygen evolution reaction (OER) and especially the oxygen reduction reaction (ORR) in the aprotic Li/air battery system has not yet been clarified. Here, three nanostructured manganese oxide catalysts - namely Mn3O4, Mn5O8 and alpha-Mn2O3 - are investigated with regard to their activity for the ORR in a LiTFSI/DMSO electrolyte. In cyclic voltammetry (CV) measurements an overall decrease of potential gaps and an increase of re-oxidation efficiencies on carbon powder-based electrodes in comparison to glassy carbon (GC) was observed, which is attributed to the presence of more active centers, e.g. edges and kinks. Increased ORR potentials and the kinetic evaluation of the rate-determining step, namely the one-electron reduction of oxygen, point to a significantly enhanced activity of alpha-Mn2O3/C compared to pure carbon powder, Mn3O4/C and Mn5O8/C electrodes. This is discussed in terms of the electrocatalytic effect of alpha-Mn2O3 for aprotic ORR processes. The ORR activity is proposed to originate from a different reaction pathway due to coordinatively unsaturated Mn3+ ions on the surface of alpha-Mn2O3, which act as active centers for associative adsorption and reduction of molecular O-2. (C) 2015 Elsevier Ltd. All rights reserved.
机译:尽管在过去十年中在催化剂研究上付出了巨大的努力,但对于非质子型锂/空气电池系统中的氧气释放反应(OER),尤其是氧气还原反应(ORR),电催化剂的益处尚未阐明。在此,研究了三种纳米结构的锰氧化物催化剂-Mn3O4,Mn5O8和α-Mn2O3-在LiTFSI / DMSO电解质中对ORR的活性。在循环伏安法(CV)测量中,与玻璃碳(GC)相比,观察到碳粉基电极上电势差的总体降低和重氧化效率的提高,这归因于存在更多的活性中心,例如边缘和扭结。与纯碳粉,Mn3O4 / C和Mn5O8 / C电极相比,增加的ORR电位和速率确定步骤的动力学评估(即氧的单电子还原)表明α-Mn2O3/ C的活性显着增强。关于α-Mn2O3对非质子ORR过程的电催化作用进行了讨论。有人提出ORR活性源自不同的反应途径,这是由于α-Mn2O3表面上的配位不饱和Mn3 +离子充当了相关吸附和分子O-2还原的活性中心。 (C)2015 Elsevier Ltd.保留所有权利。

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