Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/154940
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dc.contributor.authorFernàndez Altable, Víctor-
dc.contributor.authorDalmases Solé, Mariona-
dc.contributor.authorFalqui, Andrea-
dc.contributor.authorCasu, Alberto-
dc.contributor.authorTorruella Besa, Pau-
dc.contributor.authorEstradé Albiol, Sònia-
dc.contributor.authorPeiró Martínez, Francisca-
dc.contributor.authorFiguerola i Silvestre, Albert-
dc.date.accessioned2020-04-03T10:38:13Z-
dc.date.available2020-04-03T10:38:13Z-
dc.date.issued2015-02-03-
dc.identifier.issn0897-4756-
dc.identifier.urihttp://hdl.handle.net/2445/154940-
dc.description.abstractThe optimization of a material functionality requires both the rational design and precise engineering of its structural and chemical parameters. In this work, we show how colloidal chemistry is an excellent synthetic choice for the synthesis of novel ternary nanostructured chalcogenides, containing exclusively noble metals, with tailored morphology and composition and with potential application in the energy conversion field. Specifically, the Ag-Au-Se system has been explored from a synthetic point of view, leading to a set of Ag2Se-based hybrid and ternary nanoparticles, including the room temperature synthesis of the rare ternary Ag3AuSe2 fischesserite phase. An in-depth structural and chemical characterization of all nanomaterials has been performed, which proofed especially useful for unravelling the reaction mechanism behind the formation of the ternary phase in solution. The work is complemented with the thermal and electric characterization of a ternary Ag-Au-Se nanocomposite with promising results: we found that the use of the ternary nanocomposite represents a clear improvement in terms of thermoelectric energy conversion as compared to a binary Ag-Se nanocomposite analogue.-
dc.format.extent9 p.-
dc.format.mimetypeapplication/pdf-
dc.language.isoeng-
dc.publisherAmerican Chemical Society-
dc.relation.isformatofVersió postprint del document publicat a: https://doi.org/10.1021/cm504433y-
dc.relation.ispartofChemistry of Materials, 2015, vol. 27, num. 5, p. 1656-1664-
dc.relation.urihttps://doi.org/10.1021/cm504433y-
dc.rights(c) American Chemical Society , 2015-
dc.sourceArticles publicats en revistes (Química Inorgànica i Orgànica)-
dc.subject.classificationNanopartícules-
dc.subject.classificationNanocristalls-
dc.subject.classificationAnisotropia-
dc.subject.classificationOr-
dc.subject.otherNanoparticles-
dc.subject.otherNanocrystals-
dc.subject.otherAnisotropy-
dc.subject.otherGold-
dc.titleAu-assisted growth of anisotropic and epitaxial CdSe colloidal nanocrystals via in-situ dismantling of quantum dots-
dc.typeinfo:eu-repo/semantics/article-
dc.typeinfo:eu-repo/semantics/acceptedVersion-
dc.identifier.idgrec652569-
dc.date.updated2020-04-03T10:38:13Z-
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess-
Appears in Collections:Articles publicats en revistes (Química Inorgànica i Orgànica)

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