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首页> 外文期刊>Electrocatalysis >Effect of Lithium and Potassium Cations on the Electrocatalytic Properties of Carbon and Manganese Oxide Electrocatalysts Towards the Oxygen Reduction Reaction in Concentrated Alkaline Electrolyte
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Effect of Lithium and Potassium Cations on the Electrocatalytic Properties of Carbon and Manganese Oxide Electrocatalysts Towards the Oxygen Reduction Reaction in Concentrated Alkaline Electrolyte

机译:锂和钾阳离子对浓碱电解质氧化锰电解质氧化锰电解质电催化性能的影响

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摘要

The impact of alkaline cations (Li~+ and K~+) on the electrocatalytic properties of high-surface-area carbon (HSAC) and nanometric manganese oxides (MnOx) deposited onto HSAC (MnOx/C) used as oxygen reduction reaction (ORR) electrodes has been studied in concentrated LiOH or KOH media. The electrochemical characterizations firstly reveal that HSAC have good ORR electrocatalytic properties in these strong alkaline electrolytes, in agreement with the literature. However, although MnOx/C exhibits high ORR activity in NaOH and KOH media below 1 M (Roche et al., J Phys Chem C 111:1434, 2007), the present study reveals their deactivation in concentrated LiOH or KOH electrolytes because of an insufficient activity of water. The latter is indeed not compatible with a sufficient presence of protons in solution, thereby limiting the necessary proton insertion into the MnOx lattice, a prerequisite for ORR activity (Roche et al., J Phys Chem C 111:1434, 2007). In addition, when LiOH electrolyte is used, another effect penalizes the electrode performances; Li~+ ions may insert into the MnOx lattice and stabilize both the Mn atoms at the oxidation state 3 and the oxygen groups at the carbon surface, which prevents their role of redox mediating species and further blocks the catalytic process, eventually yielding increased ORR overpotential.
机译:碱性阳离子(Li +和K〜+)对高表面积碳(HSAC)和纳米锰氧化物(MNOX)的电催化性能的影响,其沉积在HSAC(MNOX / C)上用作氧还原反应(ORR )已经在浓缩的LiOH或KOH培养基中研究了电极。电化学特征首先揭示了HSAC在这些强碱电解质中具有良好的ORR电催化性质,与文献一致。然而,虽然Mnox / C在1M以下在NaOH和Koh培养基中表现出高ORR活性(Roche等,J Phys Chem C 111:1434,2007),但本研究表明,由于浓缩的LiOH或KOH电解质,它们揭示了它们的失活水的不足。后者确实与溶液中的质子的足够存在不相容,从而将必要的质子插入晶格晶格(Roche等人,J Malic Chem C 111:1434,2007)限制到Mnox晶格中的必要质子插入,这是orr活性的先决条件(roche等,jthe等,j malic chem c 111:1434,2007)。另外,当使用LiOH电解质时,另一个效果惩罚电极性能; Li〜+离子可以插入Mnox晶格中并稳定在氧化态3处的Mn原子和碳表面的氧气基团,这防止其氧化还原介质物种的作用,并进一步阻断催化过程,最终产生增加的ORR过幂。

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