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dc.contributor.authorNi, Chengsheng
dc.contributor.authorZhou, Jun
dc.contributor.authorZhang, Ziye
dc.contributor.authorLi, Shuangbin
dc.contributor.authorNi, Jiupai
dc.contributor.authorWu, Kai
dc.contributor.authorIrvine, John T. S.
dc.date.accessioned2022-11-09T00:41:41Z
dc.date.available2022-11-09T00:41:41Z
dc.date.issued2021-12-01
dc.identifier.citationNi , C , Zhou , J , Zhang , Z , Li , S , Ni , J , Wu , K & Irvine , J T S 2021 , ' Iron-based electrode materials for solid oxide fuel cells and electrolysers ' , Energy & Environmental Science , vol. 14 , no. 12 , pp. 6287-6319 . https://doi.org/10.1039/d1ee01420jen
dc.identifier.issn1754-5692
dc.identifier.otherPURE: 277001290
dc.identifier.otherPURE UUID: 9d2e276b-9b2c-42c1-a2ff-4940af673b9e
dc.identifier.otherJisc: ea84e6a101d5487b84cf23c94b121e40
dc.identifier.otherScopus: 85121235639
dc.identifier.otherWOS: 000722312900001
dc.identifier.urihttps://hdl.handle.net/10023/26339
dc.descriptionWe would like to acknowledge the support from the National Natural Science Foundation of China (NSFC, 51702264, 41371275, 51877173, 51737011), the Fundamental Research Funds for the Central Universities (XDJK2020B066; SWURC2020002) and EPSRC (EP/R023522/1, EP/P024807/1). We also thank the funding from Chongqing Committee of S&T (grant No. cstc2021ycjhbgzxm0162). C. N. also acknowledges the support from Bayu Scholar for Young Teachers.en
dc.description.abstractA critical new research direction in solid oxide cells (SOCs) is related to balancing power-grid load or integrating heat-electricity-gas interconnection simply by switching operations between the fuel-cell and electrolyser mode. The rational design of robust and high-performance materials for SOCs is urgent for high conversion/energy efficiencies. Iron is highly abundant and offers suitable and flexible redox chemistry for the two operation modes. Iron-based oxide materials are widely investigated for SOCs because of their low cost and, more importantly, the appropriate valence stability of the Fe–O bond for excellent redox activity across a wide range of electrode functions. This review describes the progress in iron-based materials for SOCs, especially the recent applications in electrode materials or catalysts. The stable structure of the ferrite oxides provides an important platform for improved performance via the substitution of Fe in the fuel electrodes of an SOC with H2/H2O or carbonaceous fuel/feedstock. Furthermore, we discuss nano-sized Fe0 metal or alloys on an oxide electrode via infiltration and in situ exsolution aiming to fabricate highly active electrocatalysts. The advances of ferrite oxide-based oxygen electrodes are also discussed in terms of thermal expansion, stability and electrocatalysis before the developments of symmetrical and reversible SOCs based on ferrite oxides are classified and summarized. Therefore, the challenges and future prospects are discussed.
dc.format.extent33
dc.language.isoeng
dc.relation.ispartofEnergy & Environmental Scienceen
dc.rightsCopyright © 2021 The Author(s). This work has been made available online in accordance with publisher policies or with permission. Permission for further reuse of this content should be sought from the publisher or the rights holder. This is the author created accepted manuscript following peer review and may differ slightly from the final published version. The final published version of this work is available at https://doi.org/10.1039/D1EE01420Jen
dc.subjectQD Chemistryen
dc.subjectACen
dc.subject.lccQDen
dc.titleIron-based electrode materials for solid oxide fuel cells and electrolysersen
dc.typeJournal itemen
dc.contributor.sponsorEPSRCen
dc.contributor.sponsorEPSRCen
dc.description.versionPostprinten
dc.contributor.institutionUniversity of St Andrews. School of Chemistryen
dc.contributor.institutionUniversity of St Andrews. Centre for Energy Ethicsen
dc.contributor.institutionUniversity of St Andrews. Centre for Designer Quantum Materialsen
dc.contributor.institutionUniversity of St Andrews. EaSTCHEMen
dc.identifier.doihttps://doi.org/10.1039/d1ee01420j
dc.description.statusPeer revieweden
dc.date.embargoedUntil2022-11-09
dc.identifier.grantnumberEP/R023522/1en
dc.identifier.grantnumberEP/P024807/1en


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