Surface modification of electrocatalyst for optimal adsorption of reactants in oxygen evolution reaction

Abstract

Technological development after the industrial revolution has improved the quality of human life, but global energy consumption continues to increase due to population growth and the development of fossil fuels. Therefore, numerous studies have been conducted to develop sustainable long-term and renewable alternative energy sources. The anodic electrode, which is one of the two-electrode system components, is an essential element for effective energy production. In general, precious metal-based electrocatalysts show high OER reactions from the anodic electrode, but it is difficult to scale up due to their low abundance and high cost. To overcome these problems, transition metal-based anodic electrodes, which exhibit advantages with respect to their low cost and high catalytic activities, are in the spotlight nowadays. Among them, stainless steel is a material with a high ratio of transition metal components, i.e., Fe, Ni, and Cr, and has excellent corrosion resistance and low cost. However, stainless steel shows low electrochemical performance due to its slow sluggish kinetics and lack of active sites. In this study, we fabricated surface modified electrodes by two methods: (i) anodization and (ii) hydrogen peroxide (H2O2 ) immersion treatments. As a result of comparing the two methods, the change of the electrode surface and the electrochemical properties were not confirmed in the H2O2 immersion method. On the other hand, the porous electrode (PE) fabricated through electrochemical anodization shows a low charge transfer resistance (Rct ) and high OER activity due to its large surface area compared to the conventional electrode (CE). These results confirm that the synthesis process of H2O2 immersion is an unsuitable method for surface modification. In contrast, the PE fabricated by anodization can increase the OER activity by providing high adsorption of reactants through surface modification.