Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/153574
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dc.contributor.authorWang, Xiaojiangen_US
dc.contributor.authorZheng, Tianlongen_US
dc.contributor.authorTang, Yizhaoen_US
dc.contributor.authorLi, Xiaoyuen_US
dc.contributor.authorRykov, Alexandre I.en_US
dc.contributor.authorLi, Xuningen_US
dc.contributor.authorWang, Junhuen_US
dc.contributor.authorHe, Qinggangen_US
dc.contributor.authorCheng, Junen_US
dc.contributor.authorZhang, Xueen_US
dc.date.accessioned2021-12-08T06:43:18Z-
dc.date.available2021-12-08T06:43:18Z-
dc.date.issued2021-
dc.identifier.citationWang, X., Zheng, T., Tang, Y., Li, X., Rykov, A. I., Li, X., Wang, J., He, Q., Cheng, J. & Zhang, X. (2021). The effect of tuning the coordination sphere of iron complexes for the oxygen reduction reaction in acidic media. Journal of the Electrochemical Society, 168(4), 044506-. https://dx.doi.org/10.1149/1945-7111/abf21ben_US
dc.identifier.issn0013-4651en_US
dc.identifier.urihttps://hdl.handle.net/10356/153574-
dc.description.abstractAs a type of important non-precious catalyst for the oxygen reduction reaction (ORR), the regulating role of a metal centre in metal-macrocycles and other complexes for activity has been extensively studied. However, a common guideline to explain the effect of peripheral coordinated-ligands has not been reached. Herein, a series of organic iron complexes (denoted as FeL, L = TAA, Pc, TPP, Corrole, Tim and Salen) were synthesized as ORR catalysts and an explicit relationship of structure-activity was constructed. The kinetic current density for these compounds was identified to follow the order of FeTAA > FePc > FeTPP > FeCorrole > FeTim > FeSalen. An electron-transfer number close to 4 was derived for all these complexes except for FeTim and FeSalen, implying a near complete reduction of oxygen to water. X-ray absorption near edge structure spectroscopy (XANES) and Mössbauer spectroscopy were used to probe the nature of the distinct activities by investigating the iron-centre electron structures. Density function theory (DFT) calculations were carried out to study the charge redistribution across the iron complexes. Novel activity descriptors including the charge and spin densities on the Fe site were proposed and validated by available experimental data, presenting a strategy to design highly-active nonprecious metal complex catalysts with specific supporting ligands.en_US
dc.language.isoenen_US
dc.relation.ispartofJournal of the Electrochemical Societyen_US
dc.rights© The Electrochemical Society, Inc. 2021. All rights reserved. Except as provided under U.S. copyright law, this work may not be reproduced, resold, distributed, or modified without the express permission of The Electrochemical Society (ECS). The archival version of this work was published in Journal of The Electrochemical Society, 168(4), 044506-..en_US
dc.subjectEngineering::Chemical engineeringen_US
dc.titleThe effect of tuning the coordination sphere of iron complexes for the oxygen reduction reaction in acidic mediaen_US
dc.typeJournal Articleen
dc.contributor.schoolSchool of Chemical and Biomedical Engineeringen_US
dc.identifier.doi10.1149/1945-7111/abf21b-
dc.description.versionPublished versionen_US
dc.identifier.scopus2-s2.0-85105763891-
dc.identifier.issue4en_US
dc.identifier.volume168en_US
dc.identifier.spage044506en_US
dc.subject.keywordsCatalystsen_US
dc.subject.keywordsElectrolytic Reductionen_US
dc.description.acknowledgementQ.H. acknowledges the financial support from the National Natural Science Foundation of China (grant nos. 21978260, 21676241, and U1732111).en_US
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