Highly effective bi‐functional electrochemical activity of Ag2O‐PrO2/γ‐Al2O3 electrocatalysts towards OER and ORR

• Published in: International journal of energy research Vol. 46; no. 10; pp. 14161 - 14173
• Main Authors: Khan, Mariam, Janjua, Naveed Kausar, Ahmad, Awais, Luque, Rafael, Al‐Kahtani, Abdullah A., Tighezza, Ammar Mohamed
• Format: Journal Article
• Language: English
• Published: Chichester, UK John Wiley & Sons, Inc 01.08.2022; Hindawi Limited
• Subjects: Aluminum oxide; Batteries; bi‐functional electrocatalysts; Carbon; Catalysts; Chemical reduction; Coefficients; Commercialization; Corrosion; cyclic voltammetry; Diffusion; Diffusion coefficients; Electrocatalysts; Electrochemistry; Electrode materials; Electrodes; Electrons; Energy; Energy output; Energy storage; Fuel cells; Fuel technology; Kinetics; Marketing; Mass transport; nanocomposites; Oxidation; Oxygen; oxygen reduction reaction; Oxygen reduction reactions; Platinum; Praseodymium; Praseodymium oxide; Regenerative fuel cells; Silver; Voltammetry; water splitting
• ISSN: 0363-907X; 1099-114X
• DOI: 10.1002/er.8133

Summary The oxygen reduction and evolution reaction (ORR/OER), are the keystones for many energy generating and storage devices, have influence with many electrocatalytic reactions. The sluggish kinetics of these reaction is a challenging situation on the surface of electrodes which imposes large over‐potential and affects the energy output of fuel cells. Although the platinum‐based electrode materials have excellent activity toward ORR/OER but their high cost limits commercialization of fuel cells. To deal with this problem, platinum‐free electrode materials has aroused the considerations of scientists. The present work is proposed to study the oxygen reduction reaction and water oxidation on the surface of xAg2O‐yPrO2/γ‐Al2O3/Glassy‐Carbon. The ORR was studied electrochemically via cyclic voltammetry on the surface of these nano‐catalysts while the OER was investigated via cyclic voltammetry and linear sweep voltammetry in alkaline media. The mechanism of ORR on catalysts surface was enquired and the results indicate that ORR followed two electrons pathway in case of 10PrO2/γ‐Al2O3/Glassy‐Carbon while four electrons reduction pathway is identified on surface of others catalysts which divulged that addition of silver with praseodymium shifted the mechanism from 2e− to 4e− pathway. The electrocatalysts featured the stability during multiple scans and no corrosion of electrode in OER/ORR is observed. Different kinetic parameters for both reactions are determined which affirmed that both ORR and OER on the active surface of catalysts is irreversible and diffusion controlled. 4Ag2O‐6PrO2/γ‐Al2O3 is indicated to be proficient electro‐catalyst among other members of the series, having greater value of mass transport and diffusion coefficients. The bi‐functionality of all electrocatalysts are verified by their electrochemical responses in alkaline medium. The catalytic reduction of oxygen and oxidation of water by these electro‐catalysts imitates their potential as electrode material in batteries and unitized regenerative fuel cells (URFC) technology for energy production as substitute of platinum electrode. xAg2O‐yPrO2/γ‐Al2O3 are studied for electrochemical OER and ORR. These are proved to be cost‐effective and active bi‐functional electrocatalysts towards ORR/water oxidation, intimating their potential as electrode material for future perspective of URFC/batteries.