Potentiodynamic formation of diaminobenzene films on an electrochemically reduced graphene oxide surface: Determination of nitrite in water samples
Creators
- 1. Electrodics and Electrocatalysis Division, CSIR-Central Electrochemical Research Institute, Karaikudi-630 003, Tamil Nadu (India)
- 2. School of Chemical Engineering, Yeungnam University, Gyeongsan, Gyeongbuk 38541 (Korea, Republic of)
- 3. CSIR-Central Electrochemical Research Institute–Chennai Centre,CSIR–Madras Complex, Taramani, Chennai–600 113 (India)
Description
Highlights: • Novel diaminobenzene film on ERGO was fabricated by potentiodynamic method. • p-DAB@ERGO/GC shows excellent activity towards nitrite. • The proposed sensor exhibits lowest detection limit and wide linear range. • Modified electrode was successfully applied to the analysis in water samples. - Abstract: An electrode comprised of a polydiaminobenzene (p-DAB) film formed on electrochemically reduced graphene oxide (ERGO) on a glassy carbon (GC) (p-DAB@ERGO/GC) was fabricated using a potentiodynamic method for the sensitive and selective determination of nitrite in the presence of a common interference. The p-DAB@ERGO/GC film-modified electrode surfaces were characterized by scanning electron microscopy, X-ray photoelectron spectroscopy (XPS), Raman spectroscopy, electrochemical impedance spectroscopy and cyclic voltammetry. The film fabrication was initiated via the NH2 groups of DAB, which was confirmed by XPS from the peaks corresponding to NH (396.7 eV), NH (399.4 eV), NN (400.2 eV), and N+H (402.2 eV). The Raman spectra revealed the characteristic D and G bands at 1348 and 1595 cm−1, respectively, which confirmed the fabrication of GO on the GC electrode, and the ratio of the D and G bands was increased after the electrochemical reduction of GO. The surface coverage of the modified electrode was 8.16 × 10−11 mol cm−2. The p-DAB@ERGO/GC film-modified electrode was used successfully for the determination of nitrite ions. The p-DAB@ERGO/GC film-modified electrode exhibited superior activity for the determination of nitrite compared to the bare GC and p-DAB@GC electrodes. The amperometric current increased linearly with increasing nitrite concentration from 7.0 × 10−6 to 2.0 × 10−2 M. The detection limit was 30 nM (S/N = 3). In addition, the modified electrode was used successfully to determine the nitrite ion concentration in the presence of a 100-fold excess of common interferents. The practical application of the modified electrode was demonstrated by determining the nitrite ion concentration in water samples.
Availability note (English)
Available from http://dx.doi.org/10.1016/j.msec.2017.12.004Additional details
Identifiers
- DOI
- 10.1016/j.msec.2017.12.004;
- PII
- S0928493117315011;
Publishing Information
- Journal Title
- Materials Science and Engineering. C, Biomimetic Materials, Sensors and Systems
- Journal Volume
- 85
- Journal Page Range
- p. 97-106
- ISSN
- 0928-4931
INIS
- Country of Publication
- Netherlands
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 50038433
- Subject category
- S75: CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND SUPERFLUIDITY; S37: INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY;
- Descriptors DEI
- AMPEROMETRY; BENZENE; CONCENTRATION RATIO; DRINKING WATER; ELECTROCHEMISTRY; ELECTRODES; FABRICATION; GRAPHENE; IMPEDANCE; INTERFERENCE; NITRITES; OXIDES; RAMAN SPECTRA; RAMAN SPECTROSCOPY; SCANNING ELECTRON MICROSCOPY; SENSITIVITY; THIN FILMS; VOLTAMETRY; X-RAY PHOTOELECTRON SPECTROSCOPY
- Descriptors DEC
- AROMATICS; CARBON; CHALCOGENIDES; CHEMICAL ANALYSIS; CHEMISTRY; DIMENSIONLESS NUMBERS; ELECTRON MICROSCOPY; ELECTRON SPECTROSCOPY; ELEMENTS; FILMS; HYDROCARBONS; HYDROGEN COMPOUNDS; LASER SPECTROSCOPY; MICROSCOPY; NITROGEN COMPOUNDS; NONMETALS; ORGANIC COMPOUNDS; OXYGEN COMPOUNDS; PHOTOELECTRON SPECTROSCOPY; QUANTITATIVE CHEMICAL ANALYSIS; SPECTRA; SPECTROSCOPY; TITRATION; VOLUMETRIC ANALYSIS; WATER
Optional Information
- Copyright
- Copyright (c) 2017 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.