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用于析氧反应的、易于掺入掺杂剂的高活性钴基电催化剂。

Highly Active Cobalt-Based Electrocatalysts with Facile Incorporation of Dopants for the Oxygen Evolution Reaction.

作者信息

Moon Gun-Hee, Yu Mingquan, Chan Candace K, Tüysüz Harun

机构信息

Department of Heterogeneous Catalysis, Max-Planck-Institut für Kohlenforschung, Kaiser-Wilhelm-Platz 1, 45470, Mülheim an der Ruhr, Germany.

Materials Science and Engineering, School for Engineering of Matter, Transport and Energy, Arizona State University, P.O. Box 876106, Tempe, AZ, USA.

出版信息

Angew Chem Int Ed Engl. 2019 Mar 11;58(11):3491-3495. doi: 10.1002/anie.201813052. Epub 2019 Feb 6.

DOI:10.1002/anie.201813052
PMID:30664307
Abstract

In situ formation of electroactive cobalt species for the oxygen evolution reaction is simply achieved by applying an anodic bias to a commercially available cobalt precursor and Nafion binder mixture coated on a glassy carbon electrode. This preparation does not require energy-intensive materials preparation steps or noble metals, yet a low overpotential of 322 mV at 10.2 mA cm and a high current density of more than 300 mA cm at 1.7 V were obtained in 1 m KOH. An operando electrochemical Raman spectroscopy study confirmed the formation of cobalt oxyhydroxide species and the iron stimulated the equilibrium state between Co and Co . The iron present in the alkali electrolyte or ink solution effectively activated the cobalt species, and most of the first row transition metals could also enhance the catalytic performance. The concept presented here is one of the simplest strategies for preparing highly active electrocatalysts and is very flexible for the replacement of cobalt by other transition metals.

摘要

通过对涂覆在玻碳电极上的市售钴前驱体和Nafion粘合剂混合物施加阳极偏压,可简单地实现用于析氧反应的电活性钴物种的原位形成。这种制备方法不需要耗能的材料制备步骤或贵金属,然而在1 m KOH中,在10.2 mA cm时获得了322 mV的低过电位,在1.7 V时获得了超过300 mA cm的高电流密度。一项原位电化学拉曼光谱研究证实了羟基氧化钴物种的形成,并且铁促进了Co和Co之间的平衡状态。碱电解质或油墨溶液中存在的铁有效地活化了钴物种,并且大多数第一排过渡金属也可以提高催化性能。这里提出的概念是制备高活性电催化剂的最简单策略之一,并且对于用其他过渡金属替代钴非常灵活。

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