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Please use this identifier to cite or link to this item: http://lrcdrs.bennett.edu.in:80/handle/123456789/1519
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dc.contributor.authorPanda, Swarup K.-
dc.date.accessioned2023-04-10T03:37:17Z-
dc.date.available2023-04-10T03:37:17Z-
dc.date.issued2022-
dc.identifier.issn1463-9076-
dc.identifier.urihttps://doi.org/10.1039/D1CP04082K-
dc.identifier.urihttp://lrcdrs.bennett.edu.in:80/handle/123456789/1519-
dc.description.abstractGreen and sustainable energy production through renewable sources is an enormously exciting field of research. Herein, we report an A-site lanthanum doped oxygen excess ruthenate (predominantly Ru5+-ions) double perovskite system, CaLaScRuO6+d (CLSR), as an excellent photocatalyst for water splitting. The well characterized polycrystalline compound shows canted antiferromagnetic (AFM) behavior due to the existence of disordered Ru-ions at the B-site. Based on density functional theory + U (Hubbard U) calculations, we have estimated various magnetic exchange interactions and found that the ground state is antiferromagnetic in nature which is in perfect agreement with our experimental results. Detailed analysis of the electronic structure further reveals that the present system belongs to the family of charge transfer semiconductors with an energy gap of B0.45 eV. Finally, the material is found to proficiently work for the oxygen evolution reaction (OER) via visible-light driven water splitting at neutral pH in an ecofriendly manneren_US
dc.language.isoenen_US
dc.publisherRoyal Society of Chemistryen_US
dc.relation.ispartofseriesVol. 24;Issue 08-
dc.subjectAntiferromagneticallyen_US
dc.subjectsplittingen_US
dc.titleAntiferromagnetically coupled double perovskite as an efficient and robust catalyst for visible light driven water splitting at neutral pHen_US
dc.typeArticleen_US
dc.indexedSWCen_US
Appears in Collections:Journal Articles_ECE

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