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CeO2 and CeO2:Pr nanocrystalline powders prepared by the polymeric precursor method: Yellow and red pigments with tunable color

dc.contributor.authorGonzaga, Luiziana Aparecida [UNESP]
dc.contributor.authorSantana, Vinicius Tadeu
dc.contributor.authorBernardi, Maria Inês Basso
dc.contributor.authorHrubý, Jakub
dc.contributor.authorNeugebauer, Petr
dc.contributor.authorMesquita, Alexandre [UNESP]
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionBrno University of Technology
dc.contributor.institutionUniversidade de São Paulo (USP)
dc.date.accessioned2020-12-12T01:30:01Z
dc.date.available2020-12-12T01:30:01Z
dc.date.issued2020-11-01
dc.description.abstractThe development of stable and reproducible inorganic pigments is noteworthy for industrial applications mainly considering more intense shades and low toxicity. Among the various candidates to substitute non-hazardous red and yellow pigments, CeO2 and CeO2:Pr have been attracting attention because of their opacity and high-temperature stability besides being environmental-friendly and health-friendly. In this study, nanostructured CeO2 and CeO2:Pr samples were synthesized using the polymeric precursor method and structural and optical characterizations were performed. Scanning electron microscopy reveals the morphology of CeO2 nanoparticles in which the particle size ranges from 22 to 28 nm as a function of the annealing temperature. Pr-doping does not show influence on the particle size. XRD results show that CeO2 and CeO2:Pr samples crystallize in the cubic fluorite lattice with Fm3m space group. Raman spectra show the fluorite F2g mode, confirming the XRD results. With Pr-doping and the annealing of the samples, two bands are observed between 550 and 600 cm−1, which are related to the defects in the fluorite structure associated with oxygen vacancies. XPS spectra reveal an increase in the ratio of Ce3+ ions depending on the annealing temperature and Pr-doping. This increase is associated with the carbon removal from the lattice by annealing. This behavior causes a change in the hue of the powders as the annealing temperature increases. According to diffuse reflectance and colorimetric measurements, CeO2 shows a light-yellow color due to the O 2p­Ce 4f transitions whose b* parameter mainly decreases with annealing, becoming almost white. The CeO2:Pr sample exhibits a red-orange color because of the electronic transitions between 4f2 → 5d1 states of Pr3+. Upon annealing, L* and b* parameters decrease, resulting in a red-brown shade. The charge compensation or charge transfer is responsible for the modification of the hue of these pigments.en
dc.description.affiliationInstitute of Geosciences and Exact Sciences São Paulo State University (Unesp)
dc.description.affiliationCEITEC – Central European Institute of Technology Brno University of Technology
dc.description.affiliationSão Carlos Institute of Physics University of São Paulo - USP
dc.description.affiliationUnespInstitute of Geosciences and Exact Sciences São Paulo State University (Unesp)
dc.description.sponsorshipCoordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)
dc.description.sponsorshipConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
dc.description.sponsorshipIdFAPESP: 2013/12993-4
dc.format.extent6280-6288
dc.identifierhttp://dx.doi.org/10.1111/jace.17339
dc.identifier.citationJournal of the American Ceramic Society, v. 103, n. 11, p. 6280-6288, 2020.
dc.identifier.doi10.1111/jace.17339
dc.identifier.issn1551-2916
dc.identifier.issn0002-7820
dc.identifier.scopus2-s2.0-85087512248
dc.identifier.urihttp://hdl.handle.net/11449/199073
dc.language.isoeng
dc.relation.ispartofJournal of the American Ceramic Society
dc.sourceScopus
dc.subjectcerium/cerium compounds
dc.subjectnanostructures
dc.subjectpigment
dc.subjectrare earths
dc.titleCeO2 and CeO2:Pr nanocrystalline powders prepared by the polymeric precursor method: Yellow and red pigments with tunable coloren
dc.typeArtigopt
dspace.entity.typePublication
unesp.author.orcid0000-0002-2258-6140[2]
unesp.author.orcid0000-0001-8524-0959[6]
unesp.campusUniversidade Estadual Paulista (UNESP), Instituto de Geociências e Ciências Exatas, Rio Claropt

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