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Novel Composite Material [email protected](Cr): A Highly Efficient Electrocatalyst for Ascorbic Acid Oxidation

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REQUIMTE, Departamento de Química e Bioquímica, Faculdade de Ciências, Universidade do Porto, 4169-007 Porto, Portugal
Departamento de Química e Bioquímica, CQB, Faculdade de Ciências, Universidade de Lisboa, Campo Grande C8, 1749-016 Lisboa, Portugal
Cite this: ACS Appl. Mater. Interfaces 2013, 5, 24, 13382–13390
Publication Date (Web):December 5, 2013
https://doi.org/10.1021/am4042564
Copyright © 2013 American Chemical Society
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Abstract

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A novel hybrid composite material, PMo10V2@MIL-101 was prepared by the encapsulation of the tetra-butylammonium (TBA) salt of the vanadium-substituted phosphomolybdate [PMo10V2O40]5– (PMo10V2) into the porous metal-organic framework (MOF) MIL-101(Cr). The materials characterization by powder X-ray diffraction, Fourier transform infrared spectra and scanning electron microscopy confirmed the preparation of the composite material without disruption of the MOF porous structure. Pyrolytic graphite electrodes modified with the original components (MIL-101(Cr), PMo10V2), and the composite material PMo10V2@MIL-101 were prepared and their electrochemical responses were studied by cyclic voltammetry. Surface confined redox processes were observed for all the immobilized materials. MIL-101(Cr) showed one-electron reduction process due to chromium centers (CrIII→CrII), while PMo10V2 presented five reduction processes: the peak at more positive potentials is attributed to two superimposed 1-electron vanadium reduction processes (VV→VIV) and the other four peaks to Mo-centred two-electron reduction processes (MoVI→MoV). The electrochemical behavior of the composite material PMo10V2@MIL-101 showed both MIL-101(Cr) and PMo10V2 redox features, although with the splitting of the two vanadium processes and the shift of the Mo- and Cr- centered processes to more negative potentials. Finally, PMo10V2@MIL-101 modified electrode showed outstanding enhanced vanadium-based electrocatalytic properties towards ascorbic acid oxidation, in comparison with the free PMo10V2, as a result of its immobilization into the porous structure of the MOF. Furthermore, PMo10V2@MIL-101 modified electrode showed successful simultaneous detection of ascorbic acid and dopamine.

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(1) UV–vis spectra of the reaction solution during the preparation of the composite material PMo10V2@MIL-101; (2) SEM images of MIL-101 (Cr) and PMo10V2@MIL-101; and (3) Mesopore size distribution for MIL-101(Cr), PMo10V2, and PMo10V2@MIL-101. This material is available free of charge via the Internet at http://pubs.acs.org.

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