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dc.contributor.authorHu, K.
dc.contributor.authorXiao, Z.
dc.contributor.authorCheng, Yi
dc.contributor.authorYan, D.
dc.contributor.authorChen, R.
dc.contributor.authorHuo, J.
dc.contributor.authorWang, S.
dc.date.accessioned2018-02-19T07:59:56Z
dc.date.available2018-02-19T07:59:56Z
dc.date.created2018-02-19T07:13:37Z
dc.date.issued2017
dc.identifier.citationHu, K. and Xiao, Z. and Cheng, Y. and Yan, D. and Chen, R. and Huo, J. and Wang, S. 2017. Iron phosphide/N, P-doped carbon nanosheets as highly efficient electrocatalysts for oxygen reduction reaction over the whole pH range. Electrochimica Acta. 254: pp. 280-286.
dc.identifier.urihttp://hdl.handle.net/20.500.11937/65848
dc.identifier.doi10.1016/j.electacta.2017.09.131
dc.description.abstract

© 2017 Elsevier Ltd Developing electrocatalysts with both high activity and low cost for oxygen reduction reaction (ORR) has attracted much attention. Herein, we fabricated iron phosphide/N, P-doped carbon nanosheets electrocatalysts via a one-pot pyrolysis process without any post-treatments, which shows high ORR activity over the whole pH range. In alkaline solution, the optimal catalyst exhibits almost the same onset potential (0.918 V vs RHE) and half-wave potential (0.832 V vs RHE) with commercial Pt/C (20 wt %), meanwhile it shows prominent catalytic activity compared with Pt/C in acidic and neutral media. Noteworthy, the catalyst catalyzes ORR process following a one-step 4e pathway in all these media and poses better tolerance toward methanol and greater durability than Pt/C. It was proved that Fe x P (x = 1 or 2) and N, P-doped carbon synergistically contributed to the high ORR activity for the electrocatalysts. This work would broaden the application of iron phosphides in the field of electrocatalysis.

dc.publisherPergamon
dc.titleIron phosphide/N, P-doped carbon nanosheets as highly efficient electrocatalysts for oxygen reduction reaction over the whole pH range
dc.typeJournal Article
dcterms.source.volume254
dcterms.source.startPage280
dcterms.source.endPage286
dcterms.source.issn0013-4686
dcterms.source.titleElectrochimica Acta
curtin.departmentFuels and Energy Technology Institute
curtin.accessStatusFulltext not available


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