Electrocatalytic oxidation and detection of N-acetylcysteine based on magnetite/reduced graphene oxide composite-modified glassy carbon electrode
- 1. School of Chemistry and Chemical Engineering, Southeast University, Nanjing 211189 (China)
- 2. National Synchrotron Radiation Laboratory, University of Science and Technology of China, Hefei 230029 (China)
- 3. College of Science, Hebei University of Engineering, Handan 056038 (China)
- 4. School of Chemistry and Chemical Engineering, Yangzhou University, Yangzhou 225002 (China)
Description
Graphical abstract: The Fe3O4/RGO composite has been successfully synthesized by a facile one-pot in-situ procedure. With its high surface area and excellent electrocatalytic activity, the electrochemical sensor based on the composite-modified glassy carbon electrodes was fabricated and applied in detecting the process of NAC electrocatalytic oxidation. -- Highlights: • RGO/Fe3O4 composite was synthesized by a facile one-pot in-situ procedure. • The RGO/Fe3O4-modified GCE was used for electrocatalytic oxidation of NAC. • Kinetic performance and detection limit of oxidation process were investigated by using different electrochemical methods. -- Abstract: The magnetite/reduced graphene oxide (Fe3O4/RGO) composite was synthesized by a facile one-pot in-situ method and characterized by transmission electron microscopy, atomic force microscopy, vibrating sample magnetometer, X-ray powder diffraction, surface area and pore size distribution, thermogravimetric analysis, Raman spectroscopy and X-ray photoelectron spectroscopy, respectively. The composite consisted of the RGO substrate with a single-layered Fe3O4 nanoparticle film, which showed the large surface area of 352 m2 g−1 and the saturated magnetization of 26.7 emu g−1. The average diameter and coverage ratio of Fe3O4 were about 8 nm and 50%, respectively. The electrocatalytic oxidation and detection of N-acetylcysteine (NAC) based on composite-modified glassy carbon electrodes (GCE) were investigated by cyclic voltammetry, amperometry, double potential step chronoamperometry and differential pulse voltammetry. Especially, the kinetic performance of oxidation processes were estimated by the Cottrell equation, indicating the diffusion coefficient of 2.06 × 10−5 cm2 s−1 and the catalytic reaction rate constant of 3.47 × 106 cm3 mol−1 s−1. Compared with the kinetic parameters, it was found that the oxidation process included both slow absorption and quick diffusion processes. The detection limit of NAC was 1.11 × 10−5 mol L−1 in the range of 0.10–10.0 mmol L−1
Availability note (English)
Available from http://dx.doi.org/10.1016/j.electacta.2013.08.010Additional details
Identifiers
- DOI
- 10.1016/j.electacta.2013.08.010;
- PII
- S0013-4686(13)01519-3;
Publishing Information
- Journal Title
- Electrochimica Acta
- Journal Volume
- 111
- Journal Page Range
- p. 31-40
- ISSN
- 0013-4686
- CODEN
- ELCAAV
INIS
- Country of Publication
- United Kingdom
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 45055273
- Subject category
- S37: INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY;
- Descriptors DEI
- ABSORPTION; AMPEROMETRY; ATOMIC FORCE MICROSCOPY; DETECTION; ELECTRODES; FERRITES; GRAPHENE; IRON OXIDES; MAGNETITE; OXIDATION; RAMAN SPECTROSCOPY; REACTION KINETICS; SENSITIVITY; SURFACE AREA; THERMAL GRAVIMETRIC ANALYSIS; TRANSMISSION ELECTRON MICROSCOPY; VIBRATING SAMPLE MAGNETOMETERS; VOLTAMETRY; X-RAY DIFFRACTION; X-RAY PHOTOELECTRON SPECTROSCOPY
- Descriptors DEC
- CARBON; CHALCOGENIDES; CHEMICAL ANALYSIS; CHEMICAL REACTIONS; COHERENT SCATTERING; DIFFRACTION; ELECTRON MICROSCOPY; ELECTRON SPECTROSCOPY; ELEMENTS; FERRIMAGNETIC MATERIALS; GRAVIMETRIC ANALYSIS; IRON COMPOUNDS; IRON ORES; KINETICS; LASER SPECTROSCOPY; MAGNETIC MATERIALS; MAGNETOMETERS; MATERIALS; MEASURING INSTRUMENTS; MICROSCOPY; MINERALS; NONMETALS; ORES; OXIDE MINERALS; OXIDES; OXYGEN COMPOUNDS; PHOTOELECTRON SPECTROSCOPY; QUANTITATIVE CHEMICAL ANALYSIS; SCATTERING; SORPTION; SPECTROSCOPY; SURFACE PROPERTIES; THERMAL ANALYSIS; TITRATION; TRANSITION ELEMENT COMPOUNDS; VOLUMETRIC ANALYSIS
Optional Information
- Copyright
- Copyright (c) 2013 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.