An Efficient Electrocatalyst for Oxygen Evolution Reaction in Alkaline Solutions Derived from a Copper Chelate Polymer via In Situ Electrochemical Transformation

Efficient oxygen evolution reaction (OER) electrocatalysts are highly desired in the field of water electrolysis and rechargeable metal-air batteries. In this study, a chelate polymer, composed of copper (II) and dithiooxamide, was used to derive an efficient catalytic system for OER. Upon potential...

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Bibliographic Details
Main Authors: Ridwan P. Putra, Hideyuki Horino, Izabela I. Rzeznicka
Format: Article
Language:English
Published: MDPI AG 2020-02-01
Series:Catalysts
Subjects:
Online Access:https://www.mdpi.com/2073-4344/10/2/233
Description
Summary:Efficient oxygen evolution reaction (OER) electrocatalysts are highly desired in the field of water electrolysis and rechargeable metal-air batteries. In this study, a chelate polymer, composed of copper (II) and dithiooxamide, was used to derive an efficient catalytic system for OER. Upon potential sweep in 1 M KOH, copper (II) centers of the chelate polymer were transformed to CuO and Cu(OH)<sub>2</sub>. The carbon-dispersed CuO nanostructures formed a nanocomposite which exhibits an enhanced catalytic activity for OER in alkaline media. The nanocomposite catalyst has an overpotential of 280 mV (at 1 mA/cm<sup>2</sup>) and a Tafel slope of 81 mV/dec in 1M KOH solution. It has a seven-fold higher current than an IrO<sub>2</sub>/C electrode, per metal loading. A catalytic cycle is proposed, in which CuO undergoes electrooxidation to Cu<sub>2</sub>O<sub>3</sub> that further decomposes to CuO with the release of oxygen. This work reveals a new method to produce an active nanocomposite catalyst for OER in alkaline media using a non-noble metal chelate polymer and a porous carbon. This method can be applied to the synthesis of transition metal oxide nanoparticles used in the preparation of composite electrodes for water electrolyzers and can be used to derive cathode materials for aqueous-type metal-air batteries.
ISSN:2073-4344