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Smart Compositional Design of B-Site Ordered Double Perovskite for Advanced Oxygen Catalysis at Ultra-High Current Densities

Authors
Christy, MariaKwon, JiseokSubramanian, Sathya SheelaChoi, SeunggunChoi, JunghyunKim, Jung HoPaik, UngyuSong, Taeseup
Issue Date
Apr-2025
Publisher
WILEY-V C H VERLAG GMBH
Keywords
bifunctional electrocatalyst; double perovskites; electrocatalyst; oxygen catalysis; oxygen evolution reaction; oxygen reduction reaction
Citation
Small Methods, v.9, no.4, pp 1 - 12
Pages
12
Indexed
SCIE
SCOPUS
Journal Title
Small Methods
Volume
9
Number
4
Start Page
1
End Page
12
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/211106
DOI
10.1002/smtd.202401480
ISSN
2366-9608
2366-9608
Abstract
Perovskite oxides have been considered promising oxygen catalysts for oxygen reduction and evolution reactions (ORR and OER), owing to structural and compositional flexibility, and tailorable properties. Ingenious B-site ordered La1.5Sr0.5NiMn0.5Fe0.5O6 (LSNMF) double perovskite is strategically designed by simultaneously interposing Ni0.5Mn0.5 and Ni0.5Fe0.5 into B′ and B″ sites. Controlling B-site cation systematically tailors the electronic structure of the B-site cation with a d-band center (Md) upshift close to the Fermi level, increasing the overlap of the Md center and O 2p center (OP). The strong interaction of Md and Op facilitates the adsorption of oxygen and activates the lattice oxygen to participate in the OER process, thereby enhancing the ORR and OER activity. For ORR, LSNMF exhibited an onset potential of 0.9 V along with a high limiting current of −8.05 mA cm−2. At the same time, for OER at 1 m KOH, LSNMF effectively reached a maximum current density of 3000 mA cm−2. Most importantly, the difference between EORR (at −1 mA cm−2) and EOER (at 10 mA cm−2), ΔE is 0.69 V, which stands among the best of recently reported perovskites. The as-designed LSNMF is stable, efficient, lucrative, and a promising candidate for practical application.
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