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dc.contributor.authorZhang, Z.
dc.contributor.authorZhu, Y.
dc.contributor.authorZhong, Y.
dc.contributor.authorZhou, W.
dc.contributor.authorShao, Zongping
dc.date.accessioned2017-07-27T05:22:40Z
dc.date.available2017-07-27T05:22:40Z
dc.date.created2017-07-26T11:11:23Z
dc.date.issued2017
dc.identifier.citationZhang, Z. and Zhu, Y. and Zhong, Y. and Zhou, W. and Shao, Z. 2017. Anion Doping: A New Strategy for Developing High-Performance Perovskite-Type Cathode Materials of Solid Oxide Fuel Cells. Advanced Energy Materials. 7 (17): Article ID 1700242.
dc.identifier.urihttp://hdl.handle.net/20.500.11937/54920
dc.identifier.doi10.1002/aenm.201700242
dc.description.abstract

Overcoming the sluggish activity of cathode materials is critical to realizing the wide-spread application of intermediate-temperature solid oxide fuel cells. Herein, a new way is reported to tune the performance of perovskite-type materials as oxygen reduction electrodes by embedding anions (F−) in oxygen sites. The obtained perovskite oxyfluorides SrFeO3−σ−δFσ and SrFe0.9Ti0.1O3−σ−δFσ (σ = 0.05 and 0.10) show improved electrocatalytic activity compared to their parent oxides, achieving area specific resistance values of 0.875, 0.393, and 0.491 Ω cm2 for SrFeO3−δ, SrFeO2.95−δF0.05, and SrFeO2.90−δF0.10, respectively, at 600 °C in air. Such improved performance is a result of the improved bulk diffusion and surface exchange properties due to anion doping. Moreover, favorable stability in performance is also demonstrated for the F− anion-doped perovskites as oxygen reduction electrodes at 650 °C for a test period of ≈200 h. A combination of anion doping and cation doping may provide a highly attractive strategy for the future development of cathode materials.

dc.publisherWILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
dc.titleAnion Doping: A New Strategy for Developing High-Performance Perovskite-Type Cathode Materials of Solid Oxide Fuel Cells
dc.typeJournal Article
dcterms.source.issn1614-6832
dcterms.source.titleAdvanced Energy Materials
curtin.departmentDepartment of Chemical Engineering
curtin.accessStatusFulltext not available


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