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GdFeO3 Perovskite Oxide Decorated by Group X Heterometal Oxides and Bifunctional Oxygen Electrocatalysis

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Author(s)
Balamurugan, ChandranSong, SeungjinJo, HyeonjeongSeo, Junhyeok
Type
Article
Citation
ACS Applied Materials and Interfaces, v.13, no.2, pp.2788 - 2798
Issued Date
2021-01
Abstract
Bifunctional electrocatalysts for oxygen evolution reaction (OER) and oxygen reduction reaction (ORR) are necessary in the renewable energy systems. However, the kinetically slow and large energy-demanding procedures of oxygen electrocatalysis make the preparation of bifunctional catalysts difficult. In this work, we report a novel hierarchical GdFeO3 perovskite oxide of a spherelike nanostructure and surface modification with the group X heterometal oxides. The nanostructured GdFeO3 layer behaved as a bifunctional electrocatalyst in the oxygen electrocatalysis of OER and ORR. Moreover, the surface decoration with catalytically active PtOx + Ni/NiO nanoparticles enhanced the electrocatalytic performances substantially. Incorporation of mesoporous PtOx + Ni/NiO nanoparticles into the porous GdFeO3 nanostructure enlarged the electrochemically active surface area and provided the interconnected nanostructures to facilitate the OER/ORR. The nanostructures were visualized by scanning electron microscopy and transmission electron microscopy images, and the surface area and pore size of nanoparticles were analyzed from N2 adsorption/desorption isotherms. Tafel analysis indicates that surface modification effectively improves the kinetics of oxygen reactions and accordingly increases the electrocatalytic efficiency. Finally, the 2 wt % PtOx + NiO|GdFeO3 (x = 0, 1, and 2) electrode achieved the enhanced OER performance with an overpotential of 0.19 V at 10 mA/cm2 in an alkaline solution and a high turnover frequency of 0.28 s-1 at η = 0.5 V. Furthermore, the ORR activity is observed with an onset potential of 0.80 V and a half-wave potential (E1/2) of 0.40 V versus reversible hydrogen electrode. ©
Publisher
American Chemical Society
ISSN
1944-8244
DOI
10.1021/acsami.0c21169
URI
https://scholar.gist.ac.kr/handle/local/11759
Appears in Collections:
Department of Chemistry > 1. Journal Articles
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