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Role of strontium as doping agent in LaMn0.5Ni0.5O3 for oxygen electro-catalysis

Authors
Islam, MobinulJeong, Min-GiOh, In-HwanNam, Kyung-WanJung, Hun-Gi
Issue Date
25-May-2020
Publisher
ELSEVIER SCIENCE INC
Keywords
Perovskite oxide; Oxygen evolution reaction; Oxygen reduction reaction; Strontium doping; Rotating disk electrode
Citation
JOURNAL OF INDUSTRIAL AND ENGINEERING CHEMISTRY, v.85, pp 94 - 101
Pages
8
Indexed
SCIE
SCOPUS
KCI
Journal Title
JOURNAL OF INDUSTRIAL AND ENGINEERING CHEMISTRY
Volume
85
Start Page
94
End Page
101
URI
https://scholarworks.dongguk.edu/handle/sw.dongguk/6606
DOI
10.1016/j.jiec.2020.01.026
ISSN
1226-086X
1876-794X
Abstract
Doping is an effective way to trigger various behaviors in ceramics. LaMn0.5Ni0.5O3 perovskites with or without strontium (Sr) doping were prepared using a sol-gel process and characterized by X-ray diffraction, X-ray photoelectron spectroscopy, scanning electron microscopy (SEM), and BrunauerEmmett-Teller (BET) gas adsorption techniques. A structural transition in the LaMn0.5Ni0.5O3 perovskite was observed upon doping, suggesting its pinning effect on the crystal structure. The SEM and BET results showed that the incorporation of Sr2+ into this oxide material markedly decreased the particle size into the nanoscale range and increased the active surface area. The oxide electrocatalytic properties toward the oxygen reduction reaction (ORR) and oxygen evolution reaction (OER) in an alkaline medium were measured using a rotating disk electrode. The results revealed that La0.8Sr0.2Ni0.5Mn0.5O3 is a more active catalyst than LaMn0.5Ni0.5O3 for the ORR and OER. The improved electrocatalytic performance of the Sr-doped oxide is related to the increase in ORR/OER current density and the positive shift in the ORR onset potential compared with that of the LaMn0.5Ni0.5O3 catalyst. The overall electron transfer number was measured as approximately 4. The basis of this enhanced performance is discussed in terms of the material electronic structure and morphology. (C) 2020 The Korean Society of Industrial and Engineering Chemistry. Published by Elsevier B.V. All rights reserved.
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