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dc.contributor.authorChen, Z
dc.contributor.authorGao, X
dc.contributor.authorWei, X
dc.contributor.authorWang, X
dc.contributor.authorLi, Y
dc.contributor.authorWu, T
dc.contributor.authorGuo, J
dc.contributor.authorGu, Q
dc.contributor.authorWu, WD
dc.contributor.authorChen, XD
dc.contributor.authorWu, Z
dc.contributor.authorZhao, D
dc.date.accessioned2021-09-07T05:56:26Z
dc.date.available2021-09-07T05:56:26Z
dc.date.issued2017
dc.identifier.issn0008-6223
dc.identifier.doi10.1016/j.carbon.2017.05.078
dc.identifier.urihttp://hdl.handle.net/10072/407717
dc.description.abstractPorous carbon materials doped with nano-sized transition metal carbides and/or metal-nitrogen coordinative sites are promising oxygen reduction electrocatalysts. The doping of such functionalities in carbon materials with desirable concentration, ultra-small size and stable configuration is still a challenge. In this paper, by grinding and pyrolyzing solid mixtures of an amino acid, an iron salt, and a mesoporous silica template, we demonstrate a solvent-free assembly approach to directly anchor both Fe3C nanoclucters and FeNx sites into nitrogen-doped ordered mesoporous graphitic carbon materials. The carbonaceous electrocatalysts are imparted with several fascinating features, namely, highly dispersed ultra-small Fe3C nanoclusters of 1–3 nm, well-anchored FeNx sites, nitrogen-doped well-graphitized carbon frameworks, and ordered mesopores (∼5.4 nm) and high surface areas (>1000 m2/g), respectively. The combination of these features makes these electrocatalysts exceptional for oxygen reduction reaction under both alkaline and acidic electrolytes, i.e. superior catalytic activities (e.g. onset and half-wave potentials up to 1.00 and 0.89 V vs. the reversible hydrogen electrode in alkaline solution), outstanding stabilities and excellent methanol tolerance, respectively. An in-depth study has been conducted to identify and characterize the key active sites in these electrocatalysts and to elucidate several important influencing factors to optimize the catalytic performance.
dc.description.peerreviewedYes
dc.languageen
dc.publisherElsevier
dc.relation.ispartofpagefrom143
dc.relation.ispartofpageto153
dc.relation.ispartofjournalCarbon
dc.relation.ispartofvolume121
dc.subject.fieldofresearchPhysical sciences
dc.subject.fieldofresearchChemical sciences
dc.subject.fieldofresearchEngineering
dc.subject.fieldofresearchcode51
dc.subject.fieldofresearchcode34
dc.subject.fieldofresearchcode40
dc.titleDirectly anchoring Fe3C nanoclusters and FeNx sites in ordered mesoporous nitrogen-doped graphitic carbons to boost electrocatalytic oxygen reduction
dc.typeJournal article
dc.type.descriptionC1 - Articles
dcterms.bibliographicCitationChen, Z; Gao, X; Wei, X; Wang, X; Li, Y; Wu, T; Guo, J; Gu, Q; Wu, WD; Chen, XD; Wu, Z; Zhao, D, Directly anchoring Fe3C nanoclusters and FeNx sites in ordered mesoporous nitrogen-doped graphitic carbons to boost electrocatalytic oxygen reduction, Carbon, 2017, 121, pp. 143-153
dc.date.updated2021-09-07T05:55:13Z
gro.hasfulltextNo Full Text
gro.griffith.authorZhao, Dongyuan


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