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Meso-tetra(4-sulfonatophenyl)porphyrin silver/Ag nanoparticles/graphene-phase C3N4 with a sandwich-like structure and double-faced active centers via two-step room-temperature photocatalytic synthesis for ractopamine detection.
Weng, Xuehua; Ye, Huiling; Xie, Wenqiang; Ying, Meihui; Pan, Haibo; Du, Min.
Afiliação
  • Weng X; National & Local Joint Biomedical Engineering Research Center on Photodynamics Technology Fuzhou Fujian 350108 P. R. China.
  • Ye H; College of Chemistry, Fuzhou University Qishan Campus Fuzhou Fujian 350108 China hbpan@fzu.edu.cn.
  • Xie W; National & Local Joint Biomedical Engineering Research Center on Photodynamics Technology Fuzhou Fujian 350108 P. R. China.
  • Ying M; College of Chemistry, Fuzhou University Qishan Campus Fuzhou Fujian 350108 China hbpan@fzu.edu.cn.
  • Pan H; National & Local Joint Biomedical Engineering Research Center on Photodynamics Technology Fuzhou Fujian 350108 P. R. China.
  • Du M; College of Chemistry, Fuzhou University Qishan Campus Fuzhou Fujian 350108 China hbpan@fzu.edu.cn.
Nanoscale Adv ; 3(13): 3900-3908, 2021 Jun 30.
Article em En | MEDLINE | ID: mdl-36133022
Photochemical synthesis under visible light irradiation is a novel approach in the field of green chemistry, and composites with abundant active centers for electrochemical detection are highly attractive. Herein, a meso-tetra(4-sulfonatophenyl)porphyrin silver/Ag nanoparticles/graphene phase C3N4 nanosheets (Ag2TPPS4/AgNPs/ng-C3N4) material with a sandwich-like structure was synthesized using a two-step photocatalytic reaction at room temperature (25 °C). In the first visible light irradiation step and in the presence of a hole capture agent, Ag+ ions were photocatalytically reduced onto the surface of ng-C3N4 that was used as a photocatalyst. Then, the protons (H+) in the core of H2TPPS4 were substituted in situ by photo-oxidized Ag+ during the second visible light irradiation step and in the presence of an electron capture agent. The electrochemical response of Ag2TPPS4 and ng-C3N4 to ractopamine (RAC) results in the unique double-faced active centers of Ag2TPPS4/AgNPs/ng-C3N4, and the cores (AgNPs) are beneficial as bridges for the connection between Ag2TPPS4 and ng-C3N4 and for high-efficiency electron transfer. Hence, as-synthesized Ag2TPPS4/AgNPs/ng-C3N4 exhibits high sensitivity (a low detection limit of 5.1 × 10-8 M, S/N = 3.0), a wide linear range (1 × 10-7 to 1.2 × 10-5 M), and long-term stability. Based on the experimental verification of the electrochemical dynamics and electrostatic attraction at the interface between the dual-active-center surface and RAC, the electrochemical mechanism has been clarified. Specifically, in the multi-cycle oxidation of RAC, the blue shift of specific UV-vis peaks also confirms the electrocatalytic oxidation of the two terminal hydroxyl groups of RAC. In brief, Ag2TPPS4/AgNPs/ng-C3N4 with a sandwich-like structure and double-faced active centers enhances the detection sensitivity and electrocatalytic efficiency towards RAC.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies Idioma: En Revista: Nanoscale Adv Ano de publicação: 2021 Tipo de documento: Article País de publicação: Reino Unido

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies Idioma: En Revista: Nanoscale Adv Ano de publicação: 2021 Tipo de documento: Article País de publicação: Reino Unido