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Bifunctional atomic iron-based catalyst for oxygen electrode reactions

机译:双官能原子铁基氧电极反应催化剂

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Development of high-efficiency atomic transition metal catalysts for oxygen electrode reactions is attractive for regenerative energy conversion and storage technologies. Here we report a facile approach to fabricate an atomic iron- and nitrogen-codoped graphene catalyst with high content of iron (up to 1.5 wt%). The atomic iron-based catalyst on glassy carbon electrodes displays low overpotential (194 mV and 275 mV) reported at 10 mA cm(-2) in 1.0 M KOH and 0.1 M KOH solutions for the oxygen evolution reaction (OER), respectively. In addition, the atomic iron-based composite electrocatalyst exhibits a high half-wave potential of 0.90 V vs. RHE for the oxygen reduction reaction (ORR) in 0.1 M KOH, and a combined ORR and OER potential gap of 0.605 V. Structural characterization and theoretical calculations demonstrate that the efficient active sites for OER and ORR should be FeN4-moiety embedded into the graphene, on which the overpotential-determining step is the O-O coupling step. (C) 2019 Elsevier Inc. All rights reserved.
机译:用于氧电极反应的高效原子过渡金属催化剂的研制对于再生能量转换和储存技术具有吸引力。在这里,我们报告了一种容易的方法来制造具有高含量的铁(高达1.5wt%)的原子铁和氮编码的石墨烯催化剂。玻璃碳电极上的原子铁基催化剂在1.0M KOH和0.1M KOH溶液中以10mA cm(-2)表示的低过电(194mV和275mV)分别用于氧气进化反应(oer)。此外,原子铁基复合电催化剂表现出0.90V与RHE的高半波电位为0.1M KOH的氧还原反应(ORR),以及0.605V的组合ORR和OER电位差距。结构表征理论计算表明,OER和ORR的有效活性位点应该是嵌入石墨烯的FEN4部分,其中过电势确定步骤是OO耦合步骤。 (c)2019 Elsevier Inc.保留所有权利。

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