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dc.contributor.author HERNANDEZ MOLINA, ROSABRIL
dc.contributor.author HERNANDEZ MARQUEZ, JUAN OMAR
dc.contributor.author ENRIQUEZ CARREJO, JOSE LUIS
dc.contributor.author FARIAS MANCILLA, JOSE RURIK
dc.contributor.author MANI GONZALEZ, PIERRE GIOVANNI
dc.contributor.author VIGUERAS SANTIAGO, ENRIQUE
dc.contributor.author RODRIGUEZ ARANDA, MA DEL CARMEN
dc.contributor.author Vargas Ortíz, Ramón Álvaro
dc.contributor.author YAÑEZ LIMON, JOSE MARTIN
dc.creator HERNANDEZ MOLINA, ROSABRIL; 420537
dc.creator HERNANDEZ MARQUEZ, JUAN OMAR; 567273
dc.creator ENRIQUEZ CARREJO, JOSE LUIS; 355799
dc.creator FARIAS MANCILLA, JOSE RURIK; 121190
dc.creator MANI GONZALEZ, PIERRE GIOVANNI; 176393
dc.creator VIGUERAS SANTIAGO, ENRIQUE; 25387
dc.creator RODRIGUEZ ARANDA, MA DEL CARMEN; 160012
dc.creator Vargas Ortíz, Ramón Álvaro; 44876
dc.creator YAÑEZ LIMON, JOSE MARTIN; 14570
dc.date.accessioned 2016-08-09T19:14:33Z
dc.date.available 2016-08-09T19:14:33Z
dc.date.issued 2015
dc.identifier http://www.redalyc.org/articulo.oa?id=94245280004
dc.identifier.uri http://hdl.handle.net/20.500.11799/54716
dc.description Actually, lithium niobate (LiNbO3) has been used for optical wavelength conversion and ultrafast optical signal processing because of its outstanding rapid nonlinear optical response behavior, low switching power and broad conversion bandwidth. LiNbO3nanoparticles, which belong to the ferroelectric oxide class, were synthesized by chemical reaction with wetchemistry. Their sizedistributionwascenteredaround200 nm. Xray diffraction (XRD) and scanning electron microscopy (SEM) were used to further investigate the quality of the obtained LiNbO3powders.The present work shows thatby employingthis chemical method the correct stoichiometric phasewas obtained. This wascorroborated by XPS (X-Ray Photoelectron Spectroscopy) results. Also, the nanoparticles showed a defined crystallinity and uniform morphology. This way of obtaining nanoparticles is innovative because of its low cost and simple way to reproduce it. It isan important method of increasing the surfacearea, controlling thephase purityand reducing theparticle size distribution. The samples were obtained under low temperature annealing at500, 650 and 800 ºC. Those features can be controlled using variables such temperature, time of synthesis,and calcination. In previous worksit wasfound that hydrothermal methods offer many advantages over conventional ceramic synthesis methods.
dc.format application/pdf
dc.language.iso eng es
dc.publisher Sociedad Mexicana de Ciencia y Tecnología de Superficies y Materiales A.C.
dc.relation http://www.redalyc.org/revista.oa?id=942
dc.rights Superficies y vacío
dc.rights openAccess es
dc.rights.uri http://creativecommons.org/licenses/by-nc-nd/4.0
dc.source Superficies y vacío (México) Num.4 Vol.28
dc.subject Física, Astronomía y Matemáticas es
dc.subject LiNbO3 es
dc.subject wet chemistry es
dc.subject XRD es
dc.subject XPS es
dc.subject SEM es
dc.subject nanoparticles es
dc.subject.classification CIENCIAS FÍSICO MATEMÁTICAS Y CIENCIAS DE LA TIERRA
dc.title Synthesis by wet chemistry and characterization of LiNbO3 nanoparticles es
dc.type Artículo es
dc.ambito Internacional es
dc.audience students es
dc.audience researchers es
dc.type.conacyt article
dc.identificator 1


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  • Título
  • Synthesis by wet chemistry and characterization of LiNbO3 nanoparticles
  • Autor
  • HERNANDEZ MOLINA, ROSABRIL
  • HERNANDEZ MARQUEZ, JUAN OMAR
  • ENRIQUEZ CARREJO, JOSE LUIS
  • FARIAS MANCILLA, JOSE RURIK
  • MANI GONZALEZ, PIERRE GIOVANNI
  • VIGUERAS SANTIAGO, ENRIQUE
  • RODRIGUEZ ARANDA, MA DEL CARMEN
  • Vargas Ortíz, Ramón Álvaro
  • YAÑEZ LIMON, JOSE MARTIN
  • Fecha de publicación
  • 2015
  • Editor
  • Sociedad Mexicana de Ciencia y Tecnología de Superficies y Materiales A.C.
  • Tipo de documento
  • Artículo
  • Palabras clave
  • Física, Astronomía y Matemáticas
  • LiNbO3
  • wet chemistry
  • XRD
  • XPS
  • SEM
  • nanoparticles
  • Los documentos depositados en el Repositorio Institucional de la Universidad Autónoma del Estado de México se encuentran a disposición en Acceso Abierto bajo la licencia Creative Commons: Atribución-NoComercial-SinDerivar 4.0 Internacional (CC BY-NC-ND 4.0)

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