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dc.contributor.authorGarcía Lojo, Daniel 
dc.contributor.authorModin, Evgeny
dc.contributor.authorGómez Graña, Sergio 
dc.contributor.authorImpéror-Clerc, Marianne
dc.contributor.authorChuvilin, Andrey
dc.contributor.authorPastoriza Santos, Isabel 
dc.contributor.authorPérez Juste, Jorge 
dc.contributor.authorConstantin, Doru
dc.contributor.authorHamon, Cyrille
dc.date.accessioned2024-02-07T14:09:59Z
dc.date.issued2021-07-02
dc.identifier.citationAdvanced Functional Materials, 31(27): 2101869 (2021)spa
dc.identifier.issn1616301X
dc.identifier.issn16163028
dc.identifier.urihttp://hdl.handle.net/11093/6067
dc.description.abstractOrganizing nanoparticles (NPs) into periodic structures is a central goal in materials science. Despite progress in the last decades, it is still challenging to produce macroscopic assemblies reliably. In this work, the analysis of the pervaporation‐induced organization of gold octahedra into supercrystals within microfluidic channels using a combination of X‐ray scattering techniques and FIB‐SEM tomography is reported. The results reveal the formation of a single‐domain supercrystal with a monoclinic C2/m symmetry and long‐range order extending over the dimensions of the microfluidic channel, covering at least 1.7 × 0.3 mm 2 . Time‐resolved small angle X‐ray scattering analysis shows that the formation of the superlattice involves an accumulation of the NPs within the channel before the nucleation and growth of the supercrystal. The orientation of the crystal remains unchanged during its formation, suggesting a growth mechanism directed by the channel interface. Together, these results show the potential application of the pervaporation strategy to providing spatially determined control over NP crystallization, which can be used for the rational fabrication of nanomaterial architectures.spa
dc.description.sponsorshipMinisterio de Economía, Industria y Competitividad | Ref. MAT2016-77809-Rspa
dc.description.sponsorshipAgencia Estatal de Investigación | Ref. PID2019-108954RB-I00spa
dc.description.sponsorshipXunta de Galicia | Ref. GRC ED431C 2016–048spa
dc.description.sponsorshipAgencia Estatal de Investigación | Ref. BES-2017-081670spa
dc.description.sponsorshipAgencia Estatal de Investigación | Ref. IJCI-2016-29108spa
dc.language.isoengspa
dc.publisherAdvanced Functional Materialsspa
dc.relationinfo:eu-repo/grantAgreement/MINECO//MAT2016-77809-R/ES/
dc.relationinfo:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2017-2020/PID2019-108954RB-I00/ES
dc.rightsReservados todos os dereitos
dc.titleStructure and formation kinetics of millimeter‐size single domain supercrystalsen
dc.typearticlespa
dc.rights.accessRightsclosedAccessspa
dc.identifier.doi10.1002/adfm.202101869
dc.identifier.editorhttps://onlinelibrary.wiley.com/doi/10.1002/adfm.202101869spa
dc.publisher.departamentoQuímica Físicaspa
dc.publisher.grupoinvestigacionNanoBioMateriais Funcionaisspa
dc.subject.unesco2307 Química Físicaspa
dc.date.embargoEndDateindefinidospa
dc.date.updated2024-02-06T10:45:16Z
dc.computerCitationpub_title=Advanced Functional Materials|volume=31|journal_number=27|start_pag=2101869|end_pag=spa


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