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Lanthanum Ferrite Ceramic Powders: Synthesis, Characterization and Electrochemical Detection Application
The perovskite-type lanthanum ferrite, LaFeO , has been prepared by thermal decomposition of obtained lanthanum ferrioxalate compound precursor, LaFe(C O ) ·3H O. The oxalate precursor was synthesized through the redox reaction between 1,2-ethanediol and nitrate ion and characterized by chemical ana...
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Published in: | Materials 2020-04, Vol.13 (9), p.2061 |
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Main Authors: | , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | The perovskite-type lanthanum ferrite, LaFeO
, has been prepared by thermal decomposition of
obtained lanthanum ferrioxalate compound precursor, LaFe(C
O
)
·3H
O. The oxalate precursor was synthesized through the redox reaction between 1,2-ethanediol and nitrate ion and characterized by chemical analysis, infrared spectroscopy, and thermal analysis. LaFeO
obtained after the calcination of the precursor for at least 550-800 °C/1 h have been investigated by X-ray diffraction (XRD), field emission scanning electron microscopy (FE-SEM), transmission electron microscopy (TEM), and high-resolution transmission electron microscopy (HRTEM). A boron-doped diamond electrode (BDD) modified with LaFeO
ceramic powders at 550 °C (LaFeO
/BDD) by simple immersion was characterized by cyclic voltammetry and tested for the voltammetric and amperometric detection of capecitabine (CCB), which is a cytostatic drug considered as an emerging pollutant in water. The modified electrode exhibited a complex electrochemical behaviour by several redox systems in direct relation to the electrode potential range. The results obtained by cyclic voltammetry (CV), differential-pulsed voltammetry (DPV), and multiple-pulsed amperometry proved the electrocatalytic effect to capecitabine oxidation and reduction and allowed its electrochemical detection in alkaline aqueous solution. |
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ISSN: | 1996-1944 1996-1944 |
DOI: | 10.3390/ma13092061 |