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dc.contributor.authorTeixeira, Mayara Mondego
dc.contributor.authorOliveira, Regiane
dc.contributor.authorCarvalho de Oliveira, Marisa
dc.contributor.authorRibeiro, Renan
dc.contributor.authorde Lazaro, Sergio Ricardo
dc.contributor.authorLi, Maximo Siu
dc.contributor.authorChiquito, Adenilson J.
dc.contributor.authorGracia, Lourdes
dc.contributor.authorAndres, Juan
dc.contributor.authorLongo, Elson
dc.date.accessioned2019-02-13T10:00:11Z
dc.date.available2019-02-13T10:00:11Z
dc.date.issued2018-11
dc.identifier.citationTEIXEIRA, Mayara Mondego, et al. Computational Chemistry Meets Experiments for Explaining the Geometry, Electronic Structure, and Optical Properties of Ca10V6O25. Inorganic chemistry, 2018, 57.24: 15489-15499.ca_CA
dc.identifier.urihttp://hdl.handle.net/10234/181032
dc.description.abstractIn this paper, we present a combined experimental and theoretical study to disclose, for the first time, the structural, electronic, and optical properties of Ca10V6O25 crystals. The microwave-assisted hydrothermal (MAH) method has been employed to synthesize these crystals with different morphologies, within a short reaction time at 120 °C. First-principle quantum mechanical calculations have been performed at the density functional theory level to obtain the geometry and electronic properties of Ca10V6O25 crystal in the fundamental and excited electronic states (singlet and triplet). These results, combined with the measurements of X-ray diffraction (XRD) and Rietveld refinements, confirm that the building blocks lattice of the Ca10V6O25 crystals consist of three types of distorted 6-fold coordination [CaO6] clusters: octahedral, prism and pentagonal pyramidal, and distorted tetrahedral [VO4] clusters. Theoretical and experimental results on the structure and vibrational frequencies are in agreement. Thus, it was possible to assign the Raman modes for the Ca10V6O25 superstructure, which will allow us to show the structure of the unit cell of the material, as well as the coordination of the Ca and V atoms. This also allowed us to understand the charge transfer process that happens in the singlet state (s) and the excited states, singlet (s*) and triplet (t*), generating the photoluminescence emissions of the Ca10V6O25 crystals.ca_CA
dc.format.extent12 p.ca_CA
dc.format.mimetypeapplication/pdfca_CA
dc.language.isoengca_CA
dc.publisherAmerican Chemical Societyca_CA
dc.rightsCopyright © 2018 American Chemical Societyca_CA
dc.rights.urihttp://rightsstatements.org/vocab/InC/1.0/*
dc.subjectcrystalsca_CA
dc.titleComputational Chemistry Meets Experiments for Explaining the Geometry, Electronic Structure, and Optical Properties of Ca10V6O25ca_CA
dc.typeinfo:eu-repo/semantics/articleca_CA
dc.identifier.doihttp://dx.doi.org/10.1021/acs.inorgchem.8b02807
dc.relation.projectIDCoordenação de Aperfeiçoamento de Pessoal de Nível Superior - Brasil (CAPES) - Finance Code 001 and financial support of agencies: FAPESP (2013/07296-2; 2013/26671-9), CNPq (304531/2013-8) ; Generalitat Valenciana (PrometeoII/2014/022, Prometeo/2016/079, ACOMP/2014/270, ACOMP/2015/1202) ; Ministerio de Economía y Competitividad, project CTQ2015-65207-P) ; Universitat Jaume I (UJI-B2016-25) ; Programa de Cooperación Científica con Iberoamerica (Brasil) of Ministerio de Educació (PHBP14-00020) ; GeneralitatValenciana, Santiago Grisolia Program (2015/033).ca_CA
dc.rights.accessRightsinfo:eu-repo/semantics/openAccessca_CA
dc.relation.publisherVersionhttps://pubs.acs.org/doi/abs/10.1021/acs.inorgchem.8b02807ca_CA
dc.date.embargoEndDate2019-11
dc.contributor.funderUEPG, CAPES and Fundação Araucariaca_CA
dc.type.versioninfo:eu-repo/semantics/acceptedVersionca_CA


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