4.8 Article

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

Journal

ACS APPLIED MATERIALS & INTERFACES
Volume 13, Issue 2, Pages 2788-2798

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsami.0c21169

Keywords

GdFeO3; perovskite oxide; group X heterometal oxides; bifunctional; OER; ORR

Funding

  1. National Research Foundation of Korea (NRF) - Korea Government (MSIT) [2020R1C1C1007106]
  2. GIST Research Institute (GRI) grant - GIST
  3. National Research Foundation of Korea [2020R1C1C1007106] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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A novel hierarchical GdFeO3 perovskite oxide with a spherelike nanostructure and surface modification with group X heterometal oxides was reported in this study. PtOx + Ni/NiO nanoparticles decoration on the nanostructured GdFeO3 layer significantly enhanced the electrocatalytic performances for oxygen electrocatalysis. The incorporation of mesoporous PtOx + Ni/NiO nanoparticles into the porous GdFeO3 nanostructure enlarged the electrochemically active surface area and facilitated OER/ORR.
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 N-2 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 vertical bar GdFeO3 (x = 0, 1, and 2) electrode achieved the enhanced OER performance with an overpotential of 0.19 Vat 10 mA/cm(2) in an alkaline solution and a high turnover frequency of 0.28 s(-1) at eta = 0.5 V. Furthermore, the ORR activity is observed with an onset potential of 0.80 V and a half-wave potential (E-1/2) of 0.40 V versus reversible hydrogen electrode.

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