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

被引:12
作者
Augustin, Matthias [1 ,2 ]
Yezerska, Olga [1 ]
Fenske, Daniela [1 ]
Bardenhagen, Ingo [1 ]
Westphal, Anne [1 ]
Knipper, Martin [2 ]
Plaggenborg, Thorsten [2 ]
Kolny-Olesiak, Joanna [2 ]
Parisi, Juergen [2 ]
机构
[1] Fraunhofer Inst Mfg Technol & Adv Mat, D-28359 Bremen, Germany
[2] Carl von Ossietzky Univ Oldenburg, Dept Phys, Energy & Semicond Res Lab, D-26111 Oldenburg, Germany
关键词
Mn3O4; Mn5O8; alpha-Mn2O3; ORR mechanism; aprotic electrolyte; LI-O-2; BATTERIES; OXIDATION; ELECTROCATALYSTS; RECHARGEABILITY; LITHIUM; PHASES; CARBON;
D O I
10.1016/j.electacta.2015.01.163
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
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.
引用
收藏
页码:383 / 389
页数:7
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