@article{c6c5ff00881f44249ea02fc066eb6c41,
title = "Highly Active Cobalt-Based Electrocatalysts with Facile Incorporation of Dopants for the Oxygen Evolution Reaction",
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 −2 and a high current density of more than 300 mA cm −2 at 1.7 V NHE 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 3+ and Co 4+ . 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.",
keywords = "Nafion, cobalt, electrocatalysis, oxygen evolution reaction, transition metals",
author = "Moon, {Gun hee} and Mingquan Yu and Candace Chan and Harun T{\"u}ys{\"u}z",
note = "Funding Information: This work was supported by the MAXNET Energy research consortium of the Max Planck Society and the Carbon2Chem project funded by the Bundesministerium f{\"u}r Bildung und Forschung (BMBF) and the Deutsche Forschungsgemein-schaft (DFG, German Research Foundation) under Germany≫s Excellence Strategy—EXC-2033—Projektnummer 390677874. C.K.C. would like to thank the Alexander von Humboldt Foundation for support of this work through aHumboldt Research Fellowship. We thank Adrian Schlueter for TEM and EDX analyses. Funding Information: This work was supported by the MAXNET Energy research consortium of the Max Planck Society and the Carbon2Chem project funded by the Bundesministerium f?r Bildung und Forschung (BMBF) and the Deutsche Forschungsgemeinschaft (DFG, German Research Foundation) under Germany's Excellence Strategy?EXC-2033?Projektnummer 390677874. C.K.C. would like to thank the Alexander von Humboldt Foundation for support of this work through a Humboldt Research Fellowship. We thank Adrian Schlueter for TEM and EDX analyses. Publisher Copyright: {\textcopyright} 2019 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim",
year = "2019",
month = mar,
day = "11",
doi = "10.1002/anie.201813052",
language = "English (US)",
volume = "58",
pages = "3491--3495",
journal = "Angewandte Chemie - International Edition",
issn = "1433-7851",
publisher = "John Wiley and Sons Ltd",
number = "11",
}