Metal‐Organic Gel‐Derived Co/CoO/Co3O4 Composite for the Electrochemical Detection of Diethylstilbestrol
A novel three‐phase composite of Co/CoO/Co3O4 is synthesized through straightforward calcination treatment towards cobalt‐based metal‐organic gel (Co MOG) precursor, which is constructed with the metal source of cobalt chloride and organic ligand of 4, 4', 4”‐((1, 3, 5‐triazine‐2, 4, 6‐triyl) t...
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Veröffentlicht in: | Applied organometallic chemistry 2020-04, Vol.34 (4), p.n/a |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | A novel three‐phase composite of Co/CoO/Co3O4 is synthesized through straightforward calcination treatment towards cobalt‐based metal‐organic gel (Co MOG) precursor, which is constructed with the metal source of cobalt chloride and organic ligand of 4, 4', 4”‐((1, 3, 5‐triazine‐2, 4, 6‐triyl) tris (azanediyl)) tribenzoic acid at room temperature. The morphology, structure and composition of the derived Co/CoO/Co3O4 is confirmed through scanning electron microscopy (SEM), transmission electron microscopy (TEM), powder X‐ray diffraction (XRD) and X‐ray photoelectron spectrums (XPS). Furthermore, the composite of Co/CoO/Co3O4 is employed as electrode modified material with the excellent electrochemical performances of accelerating the electron transfer and boosting the electrode interface reaction. As a proof of concept, the electrochemical redox behaviors of diethylstilbestrol (DES) have been systemically investigated at the modified electrode interface and the established analytical approach for DES with the broad linear range and satisfied recovery. This work not only provided a facile approach to obtain electrode material with excellent electrochemical performance but also enriched the application of MOG materials in the electrochemical field.
Three‐phase composite of Co/CoO/Co3O4 was obtained through one step calcination treatment towards the cobalt‐based metal organic gel (Co‐MOG), which was constructed by the metal source of CoCl2 and organic ligand of H3TATAB solution at room temperature. The derived composite acted as electrode modified material with the function of boosting charge transfer and accelerating electrode interface reaction. |
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ISSN: | 0268-2605 1099-0739 |
DOI: | 10.1002/aoc.5536 |