dc.contributor.author
Ichikawa, Rodrigo U.
dc.contributor.author
Gómez Roca, Alejandro
dc.contributor.author
López-Ortega, Alberto
dc.contributor.author
Estrader i Bofarull, Marta
dc.contributor.author
Peral Alonso, Inmaculada
dc.contributor.author
Turrillas, Xabier
dc.contributor.author
Nogués, Josep
dc.identifier
https://ddd.uab.cat/record/214184
dc.identifier
urn:10.1002/smll.201800804
dc.identifier
urn:oai:ddd.uab.cat:214184
dc.identifier
urn:scopus_id:85050506644
dc.identifier
urn:articleid:16136829v14n30a1800804
dc.identifier
urn:wos_id:000439935800005
dc.identifier
urn:icn2uab:4130239
dc.identifier
urn:oai:egreta.uab.cat:publications/2fe34f32-743e-4710-b8cd-fc58ae66249f
dc.description.abstract
Altres ajuts: Beatriu de Pinos Program (2011 BPB 00209)
dc.description.abstract
Understanding the microstructure in heterostructured nanoparticles is crucial to harnessing their properties. Although microscopy is ideal for this purpose, it allows for the analysis of only a few nanoparticles. Thus, there is a need for structural methods that take the whole sample into account. Here, a novel bulk-approach based on the combined analysis of synchrotron X-ray powder diffraction with whole powder pattern modeling, Rietveld and pair distribution function is presented. The microstructural temporal evolution of FeO/FeO core/shell nanocubes is studied at different time intervals. The results indicate that a two-phase approach (FeO and FeO) is not sufficient to successfully fit the data and two additional interface phases (FeO and FeO) are needed to obtain satisfactory fits, i.e., an onion-type structure. The analysis shows that the FeO phases grow to some extent (≈1 nm) at the expense of the FeO core. Moreover, the FeO core progressively changes its stoichiometry to accommodate more oxygen. The temporal evolution of the parameters indicates that the structure of the FeO/FeO nanocubes is rather stable, although the exact interface structure slightly evolves with time. This approach paves the way for average studies of interfaces in different kinds of heterostructured nanoparticles, particularly in cases where spectroscopic methods have some limitations.
dc.format
application/pdf
dc.relation
Agència de Gestió d'Ajuts Universitaris i de Recerca 2017/SGR-292
dc.relation
Agencia Estatal de Investigación MAT2016-77391-R
dc.relation
Ministerio de Economía y Competitividad IJCI-2014-21530
dc.relation
Ministerio de Economía y Competitividad MAT2015-67593-P
dc.relation
Ministerio de Economía y Competitividad BIA2014-57658-C2-1-R
dc.relation
Ministerio de Economía y Competitividad SEV-2013-0295
dc.relation
Small (Weinheim) ; Vol. 14, Issue 30 (July 2018), art. 1800804
dc.rights
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dc.rights
https://rightsstatements.org/vocab/InC/1.0/
dc.subject
Core/shell nanoparticles
dc.subject
Pair distribution function
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Whole powder pattern modeling
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X-ray diffraction
dc.title
Combining X-Ray Whole Powder Pattern Modeling, Rietveld and Pair Distribution Function Analyses as a Novel Bulk Approach to Study Interfaces in Heteronanostructures : Oxidation Front in FeO/Fe3O4 Core/Shell Nanoparticles as a Case Study