4.7 Article

Catalytic behavior of Pr1-xBa1+xCo2O6-δ in alkaline medium

Journal

INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
Volume 47, Issue 25, Pages 12582-12591

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.ijhydene.2022.02.002

Keywords

Electrocatalysis; Double perovskites; Oxygen evolution reaction; Oxygen reduction reaction; Cyclic voltammetry

Funding

  1. UPCST [CST-D/2273]
  2. DST-INSPIRE fellowship [IF160958, IF170554]

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A series of double perovskite oxide materials were synthesized and their catalytic activity in alkaline medium was investigated. The results show that these materials exhibit catalytic activity for both oxygen evolution reaction (OER) and oxygen reduction reactions (ORR). Among them, Pr0.90Ba1.10Co2O6-δ shows the best activity in OER.
In this work, a series of double perovskite oxide materials Pr1-xBa1+xCo2O6-delta (x = 0.05, 0.10, 0.15, and 0.20) was synthesized using the solid-state route method. Their catalytic activity and stability in 1 M KOH alkaline medium were investigated. The phase formation and structure of the prepared oxides were determined by Powder X-ray diffraction. The morphology of prepared catalysts was confirmed by SEM analysis. The catalytic performance of the prepared catalyst in alkaline solution was investigated using electrochemical measurements for both oxygen evolution reaction (OER) and oxygen reduction reactions (ORR). This series of double perovskite oxide materials exhibit catalytic activity for both OER and ORR. Pr0.90Ba1.10Co2O6-delta shows wonderful OER activity among all the catalysts with a specific capacitance of 598.40 F/g and double-layer capacitance of 38.94 mF/cm(2). Power low gives a hint of oxide-ion intercalation pseudocapacitance in the Pr0.90Ba1.10Co2O6-delta. On the other hand, Pr0.90Ba1.10Co2O6-delta exhibits potential behavior for ORR. Overall, our findings highlight the combined effects of incorporating Ba into double perovskite PrBaCo2O6-delta in its behavior for OER and ORR.(C) 2022 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.

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