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dc.contributor.author HERNANDEZ CRUZ, MARIA GUADALUPE
dc.contributor.author Solís Casados, Dora Alicia
dc.contributor.author TOLEDO ANTONIO, JOSE ANTONIO
dc.contributor.author VARGAS GARCIA, JORGE ROBERTO
dc.contributor.author ESTRADA FLORES, MIRIAM
dc.contributor.author ANGELES CHAVEZ, CARLOS
dc.contributor.author CORTES JACOME, MARIA ANTONIA
dc.contributor.author ENCARNACION GOMEZ, CECILIA
dc.creator HERNANDEZ CRUZ, MARIA GUADALUPE; 255407
dc.creator Solís Casados, Dora Alicia; 121120
dc.creator TOLEDO ANTONIO, JOSE ANTONIO; 12450
dc.creator VARGAS GARCIA, JORGE ROBERTO; 16133
dc.creator ESTRADA FLORES, MIRIAM; 331157
dc.creator ANGELES CHAVEZ, CARLOS; 20404
dc.creator CORTES JACOME, MARIA ANTONIA; 20476
dc.creator ENCARNACION GOMEZ, CECILIA; 105582
dc.date.accessioned 2023-02-15T01:35:48Z
dc.date.available 2023-02-15T01:35:48Z
dc.date.issued 2022-09-07
dc.identifier.issn 1996-1944
dc.identifier.uri http://hdl.handle.net/20.500.11799/137862
dc.description articulo es
dc.description.abstract Au nanoparticles were supported on TiO2 nanotubes by a novel vapor phase impregnation approach (VPI) using gold dimethyl-acetylacetonate as a precursor. This study aimed to evaluate the capacity of these materials in the photodecoloration of malachite green dye, with the vision to correlate the chemical, structural, morphological, and optical properties with its photocatalytic performance. The photocatalysts were characterized by X-ray diffraction, Raman spectroscopy, X-ray photoelectronic spectroscopy (XPS), electronic microscopy (HAADF-STEM and HRTEM), and UV–vis spectroscopy. The techniques mentioned above made it possible to detect the presence of small gold nanoparticles (around 3.1 nm), with a high apparent dispersion even at high metal loading for all analyzed systems. According to the XPS results, the Au nanoparticles remain reduced (Au◦ ), and they have a high electronic interaction with TiO2 , which eventually originates an electronic exchange between them and consequently a decrease in the band gap energy. In addition, the surface plasmonic resonance observed through UV–vis spectroscopy of the Au nanoparticles are factors that can be related to the high decoloration observed in these photocatalysts, specifically in the 15 wt% Au material, which achieves maximum photodecoloration of malachite green dye at 93%. es
dc.description.sponsorship This research was partially founded by the Project D.60048 “Desarrollo de un proceso catalítico para la obtención de compuestos aromáticos a partir de lignina” from Mexican Institute of Petroleum. es
dc.language.iso eng es
dc.publisher MDPI es
dc.rights openAccess es
dc.rights.uri http://creativecommons.org/licenses/by/4.0 es
dc.subject titania nanotubes es
dc.subject catalytic decoloration es
dc.subject vapor phase impregnation es
dc.subject Au nanoparticles es
dc.subject.classification BIOLOGÍA Y QUÍMICA es
dc.title Malachite Green Dye Decoloration over Au/TiO2-Nanotubes Photocatalyst under Simulate Visible-Light Irradiation es
dc.type Artículo es
dc.provenance Científica es
dc.road Verde es
dc.organismo Química es
dc.ambito Local es
dc.cve.CenCos 20403 es
dc.audience students es
dc.audience researchers es
dc.type.conacyt article
dc.identificator 2
dc.relation.vol 15 iss 18


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  • Título
  • Malachite Green Dye Decoloration over Au/TiO2-Nanotubes Photocatalyst under Simulate Visible-Light Irradiation
  • Autor
  • HERNANDEZ CRUZ, MARIA GUADALUPE
  • Solís Casados, Dora Alicia
  • TOLEDO ANTONIO, JOSE ANTONIO
  • VARGAS GARCIA, JORGE ROBERTO
  • ESTRADA FLORES, MIRIAM
  • ANGELES CHAVEZ, CARLOS
  • CORTES JACOME, MARIA ANTONIA
  • ENCARNACION GOMEZ, CECILIA
  • Fecha de publicación
  • 2022-09-07
  • Editor
  • MDPI
  • Tipo de documento
  • Artículo
  • Palabras clave
  • titania nanotubes
  • catalytic decoloration
  • vapor phase impregnation
  • Au 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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