Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/100339
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dc.contributorDepartment of Applied Physicsen_US
dc.creatorGao, Xen_US
dc.creatorLiu, Gen_US
dc.creatorZhu, Yen_US
dc.creatorKreider, Pen_US
dc.creatorBayon, Aen_US
dc.creatorGengenbach, Ten_US
dc.creatorLu, Ten_US
dc.creatorLiu, Yen_US
dc.creatorHinkley, Jen_US
dc.creatorLipiński, Wen_US
dc.creatorTricoli, Aen_US
dc.date.accessioned2023-08-08T01:55:11Z-
dc.date.available2023-08-08T01:55:11Z-
dc.identifier.issn2211-2855en_US
dc.identifier.urihttp://hdl.handle.net/10397/100339-
dc.language.isoenen_US
dc.publisherElsevieren_US
dc.rights© 2018 Elsevier Ltd. All rights reserved.en_US
dc.rights© 2018. This manuscript version is made available under the CC-BY-NC-ND 4.0 license https://creativecommons.org/licenses/by-nc-nd/4.0/en_US
dc.rightsThe following publication Gao, X., Liu, G., Zhu, Y., Kreider, P., Bayon, A., Gengenbach, T., ... & Tricoli, A. (2018). Earth-abundant transition metal oxides with extraordinary reversible oxygen exchange capacity for efficient thermochemical synthesis of solar fuels. Nano Energy, 50, 347-358 is available at https://doi.org/10.1016/j.nanoen.2018.05.045.en_US
dc.subjectEarth-abundant transition metalsen_US
dc.subjectOxygen exchange capacityen_US
dc.subjectRedox materialsen_US
dc.subjectSolar fuelsen_US
dc.subjectThermochemicalen_US
dc.subjectTransition metal carbidesen_US
dc.titleEarth-abundant transition metal oxides with extraordinary reversible oxygen exchange capacity for efficient thermochemical synthesis of solar fuelsen_US
dc.typeJournal/Magazine Articleen_US
dc.description.otherinformationTitle on author’s file: Earth-Abundant Transition Metal Oxides with Extraordinary Oxygen Exchange Capacity for Efficient Thermochemical Synthesis of Solar Fuelsen_US
dc.identifier.spage347en_US
dc.identifier.epage358en_US
dc.identifier.volume50en_US
dc.identifier.doi10.1016/j.nanoen.2018.05.045en_US
dcterms.abstractEfficient storage of solar and wind power is one of the most challenging tasks still limiting the utilization of the prime but intermittent renewable energy sources. The direct storage of concentrated solar power in renewable fuels via thermochemical splitting of water and carbon dioxide on a redox material is a scalable approach with up to 54% solar-to-fuel conversion efficiency. Despite progress, the search for earth-abundant materials that can provide and maintain high H2 and CO production rates over long period of high-temperature cycles continues. Here, we report a strategy to unlock the use of manganese, the 12th most abundant element in the Earth's crust, for thermochemical synthesis of solar fuels, achieving superior thermochemical stability, oxygen exchange capacity, and up to seven times higher mass-specific H2 and CO yield than cerium dioxide. We observe that incorporation of a small fraction of cerium ions in the manganese (II,III) oxide crystal lattice drastically increases its oxygen ion mobility, allowing its reduction from oxide to carbide during methane partial oxidation with simultaneous Ce exsolution. High CO2 and H2O splitting rates are achieved by re-oxidation of the carbide to manganese (II) oxide with simultaneous reincorporation of the cerium ions. We demonstrate that the oxide to carbide reaction is highly reversible achieving remarkable CO2 splitting rates over 100 thermochemical cycles of methane partial oxidation and CO2 splitting, and preserving the initial oxygen exchange capacity of 0.65 molO molMn −1 and 89% of the fuel production rates. Due to this extraordinarily high reversible oxygen exchange capacity, the 3% Ce-doped manganese oxide achieves an average mass-specific CO yield for CO2 splitting of 17.72 mmolCO g−1, which is significantly higher than that previously achieved in thermochemical redox cycles. More generally, these findings suggest that incorporation of small soluble amounts of cerium in earth-abundant transition metal oxides like manganese oxide is a powerful approach to enable solar thermochemical fuel synthesis.en_US
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationNano energy, Aug. 2018, v. 50, p. 347-358en_US
dcterms.isPartOfNano energyen_US
dcterms.issued2018-08-
dc.identifier.scopus2-s2.0-85047630781-
dc.identifier.eissn2211-3282en_US
dc.description.validate202308 bcvcen_US
dc.description.oaAccepted Manuscripten_US
dc.identifier.FolderNumberAP-0469-
dc.description.fundingSourceRGCen_US
dc.description.fundingSourceOthersen_US
dc.description.fundingTextThe Hong Kong Polytechnic Universityen_US
dc.description.pubStatusPublisheden_US
dc.identifier.OPUS16754765-
dc.description.oaCategoryGreen (AAM)en_US
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