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dc.citation.number 36 -
dc.citation.startPage 2101899 -
dc.citation.title ADVANCED ENERGY MATERIALS -
dc.citation.volume 11 -
dc.contributor.author Song, Yufei -
dc.contributor.author Liu, Jiapeng -
dc.contributor.author Wang, Yuhao -
dc.contributor.author Guan, Daqin -
dc.contributor.author Seong, Arim -
dc.contributor.author Liang, Mingzhuang -
dc.contributor.author Robson, Matthew J. -
dc.contributor.author Xiong, Xiandong -
dc.contributor.author Zhang, Zhiqi -
dc.contributor.author Kim, Guntae -
dc.contributor.author Shao, Zongping -
dc.contributor.author Ciucci, Francesco -
dc.date.accessioned 2023-12-21T15:17:13Z -
dc.date.available 2023-12-21T15:17:13Z -
dc.date.created 2021-08-26 -
dc.date.issued 2021-09 -
dc.description.abstract Reversible protonic ceramic cells (RePCCs) can facilitate the global transition to renewable energy sources by providing high efficiency, scalable, and fuel-flexible energy generation and storage at the grid level. However, RePCC technology is limited by the lack of durable air electrode materials with high activity toward the oxygen reduction/evolution reaction and water formation/water-splitting reaction. Herein, a novel nanocomposites concept for developing bifunctional RePCC electrodes with exceptional performance is reported. By harnessing the unique functionalities of nanoscale particles, nanocomposites can produce electrodes that simultaneously optimize reaction activity in both fuel cell/electrolysis operations. In this work, a nanocomposite electrode composed of tetragonal and Ruddlesden-Popper (RP) perovskite phases with a surface enriched by CeO2 and NiO nanoparticles is synthesized. Experiments and calculations identify that the RP phase promotes hydration and proton transfer, while NiO and CeO2 nanoparticles facilitate O-2 surface exchange and O2- transfer from the surface to the major perovskite. This composite also ensures fast (H+/O2-/e(-)) triple-conduction, thereby promoting oxygen reduction/evolution reaction activities. The as-fabricated RePCC achieves an excellent peak power density of 531 mW cm(-2) and an electrolysis current of -364 mA cm(-2) at 1.3 V at 600 degrees C, while demonstrating exceptional reversible operation stability of 120 h at 550 degrees C. -
dc.identifier.bibliographicCitation ADVANCED ENERGY MATERIALS, v.11, no.36, pp.2101899 -
dc.identifier.doi 10.1002/aenm.202101899 -
dc.identifier.issn 1614-6832 -
dc.identifier.scopusid 2-s2.0-85111745001 -
dc.identifier.uri https://scholarworks.unist.ac.kr/handle/201301/55364 -
dc.identifier.url https://onlinelibrary.wiley.com/doi/10.1002/aenm.202101899 -
dc.identifier.wosid 000681218700001 -
dc.language 영어 -
dc.publisher WILEY-V C H VERLAG GMBH -
dc.title Nanocomposites: A New Opportunity for Developing Highly Active and Durable Bifunctional Air Electrodes for Reversible Protonic Ceramic Cells -
dc.type Article -
dc.description.isOpenAccess FALSE -
dc.relation.journalWebOfScienceCategory Chemistry, Physical; Energy & Fuels; Materials Science, Multidisciplinary; Physics, Applied; Physics, Condensed Matter -
dc.relation.journalResearchArea Chemistry; Energy & Fuels; Materials Science; Physics -
dc.type.docType Article; Early Access -
dc.description.journalRegisteredClass scie -
dc.description.journalRegisteredClass scopus -
dc.subject.keywordAuthor nanocomposites -
dc.subject.keywordAuthor perovskites -
dc.subject.keywordAuthor reversible protonic ceramic cells -
dc.subject.keywordAuthor air electrodes -
dc.subject.keywordAuthor bifunctional -
dc.subject.keywordPlus OXIDE ELECTROLYSIS CELLS -
dc.subject.keywordPlus ELECTROCHEMICAL-CELLS -
dc.subject.keywordPlus LAYERED PEROVSKITES -
dc.subject.keywordPlus OXYGEN REDUCTION -
dc.subject.keywordPlus TRACER DIFFUSION -
dc.subject.keywordPlus CATHODE MATERIAL -
dc.subject.keywordPlus CO-ELECTROLYSIS -
dc.subject.keywordPlus FUEL-CELL -
dc.subject.keywordPlus GENERATION -
dc.subject.keywordPlus KINETICS -

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