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dc.contributor.authorLópez Vergara, Adrián
dc.contributor.authorEl-Refaei, S.M.
dc.contributor.authorRusso, Patricia A.
dc.contributor.authorVilchez, A
dc.contributor.authorLosilla, Enrique R.
dc.contributor.authorPorras-Vázquez, José Manuel 
dc.contributor.authorOlivera-Pastor, Pascual 
dc.contributor.authorPinna, N
dc.contributor.authorCabeza-Díaz, Aurelio 
dc.date.accessioned2019-07-19T07:13:16Z
dc.date.available2019-07-19T07:13:16Z
dc.date.created2019
dc.date.issued2019-07-19
dc.identifier.urihttps://hdl.handle.net/10630/18085
dc.description.abstractCo1-xFex-HPAA metal phosphonates were prepared and pyrolyzed under N2 and H2/Ar flows. The result-ing powders were structural and electrochemically characterised by XRD and CV, respectively. The ob-tained materials possess different structures depending on the temperature and pyrolysis atmosphere. Samples pyrolized in N2 at 1000 ºC are monophasic diphosphates, while phosphides form in H2/Ar at 850 ºC. Cyclic voltammetry studies indicate that the Co0.5Fe0.5HPAA sample, pyrolized in H2/Ar, exhibits the best behaviour, but further studies are needed to fully understand the role of graphene oxide and pyrazine.en_US
dc.description.sponsorshipUniversidad de Málaga. Campus de Excelencia Internacional Andalucía Techen_US
dc.language.isoengen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectQuímica inorgánicaen_US
dc.subject.otherElelctrocatalysisen_US
dc.subject.otherWater splittingen_US
dc.subject.otherMetal phosphonatesen_US
dc.subject.otherMetal phosphidesen_US
dc.titleSingle and solid solutions metal carboxyphosphonates as precursors for phosphorous-containing electrocatalystsen_US
dc.typeinfo:eu-repo/semantics/conferenceObjecten_US
dc.centroFacultad de Cienciasen_US
dc.relation.eventtitleHYCELTEC 2019en_US
dc.relation.eventplaceBarcelona, Españaen_US
dc.relation.eventdate01/07/2019en_US
dc.rights.ccAttribution-NonCommercial-NoDerivatives 4.0 Internacional*


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Attribution-NonCommercial-NoDerivatives 4.0 Internacional
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