Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/150964
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dc.contributor.authorShe, Sixuanen_US
dc.contributor.authorZhu, Yinlongen_US
dc.contributor.authorChen, Yuboen_US
dc.contributor.authorLu, Qianen_US
dc.contributor.authorZhou, Weien_US
dc.contributor.authorShao, Zongpingen_US
dc.date.accessioned2021-07-29T12:57:02Z-
dc.date.available2021-07-29T12:57:02Z-
dc.date.issued2019-
dc.identifier.citationShe, S., Zhu, Y., Chen, Y., Lu, Q., Zhou, W. & Shao, Z. (2019). Realizing ultrafast oxygen evolution by introducing proton acceptor into perovskites. Advanced Energy Materials, 9(20), 1900429-. https://dx.doi.org/10.1002/aenm.201900429en_US
dc.identifier.issn1614-6832en_US
dc.identifier.other0000-0002-4538-4218-
dc.identifier.urihttps://hdl.handle.net/10356/150964-
dc.description.abstractThe oxygen evolution reaction (OER) is of prime importance in multiple energy storage devices. Perovskite oxides involving lattice-oxygen oxidation are generally regarded as highly active OER catalysts, but the deprotonation of surface-bound intermediates limit the further activity improvement. Here, it is shown that this kinetic limitation can be removed by introducing Sr₃B₂O₆ (SB) which activates a proton-acceptor functionality to boost OER activity. As a proof-of-concept example, an experimental validation is conducted on the extraordinary OER performance of a Sr(Co₀.₈Fe₀.₂)₀.₇B₀.₃O₃₋δ (SCFB-0.3) hybrid catalyst, made using Sr₀.₈Co₀.₈Fe₀.₂O₃₋δ as active component and SB as a proton acceptor. This smart hybrid exhibits an exceptionally ultrahigh OER activity with an extremely low overpotential of 340 mV in 0.1 M KOH and 240 mV in 1 M KOH required for 10 mA cm⁻² which is the top-level catalytic activity among metal oxides reported so far, while maintaining excellent durability. The correlation of pH and activity study reveals that this enhanced activity mainly originates from the improved interfacial proton transfer. Such a strategy further demonstrated to be universal, which can be applied to enhance the OER activity of other high covalent oxides with close O 2p-band centers relative to Fermi energy.en_US
dc.language.isoenen_US
dc.relation.ispartofAdvanced Energy Materialsen_US
dc.rights© 2019 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim. All rights reserved.en_US
dc.subjectEngineering::Chemical engineeringen_US
dc.titleRealizing ultrafast oxygen evolution by introducing proton acceptor into perovskitesen_US
dc.typeJournal Articleen
dc.contributor.schoolSchool of Materials Science and Engineeringen_US
dc.identifier.doi10.1002/aenm.201900429-
dc.identifier.scopus2-s2.0-85063990734-
dc.identifier.issue20en_US
dc.identifier.volume9en_US
dc.identifier.spage1900429en_US
dc.subject.keywordsO 2p-band Centersen_US
dc.subject.keywordsOxygen Evolution Reactionen_US
dc.description.acknowledgementS.X.S. and Y.L.Z. contributed equally to this work. This work was supported by the Defense industrial technology development program (JCKY2018605B006), National Nature Science Foundation of China (Grant No. 21576135), and the Jiangsu Nature Science Foundation for Distinguished Young Scholars (Grant No. BK20170043).en_US
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