A screen printed carbon electrode modified with an amino-functionalized metal organic framework of type MIL-101(Cr) and with palladium nanoparticles for voltammetric sensing of nitrite
- Authors
- Vilian, A. T. Ezhil; Dinesh, Bose; Muruganantham, Rethinasabapathy; Choe, Sang Rak; Kang, Sung-Min; Huh, Yun Suk; Han, Young-Kyu
- Issue Date
- Dec-2017
- Publisher
- SPRINGER WIEN
- Keywords
- Metal-organic framework; Electrochemical sensor; Palladiumnanoparticle; Nitrite; Electro-catalysis
- Citation
- MICROCHIMICA ACTA, v.184, no.12, pp 4793 - 4801
- Pages
- 9
- Indexed
- SCI
SCIE
SCOPUS
- Journal Title
- MICROCHIMICA ACTA
- Volume
- 184
- Number
- 12
- Start Page
- 4793
- End Page
- 4801
- URI
- https://scholarworks.dongguk.edu/handle/sw.dongguk/24783
- DOI
- 10.1007/s00604-017-2513-8
- ISSN
- 0026-3672
1436-5073
- Abstract
- The authors describe an electrochemical sensor for nitrite that is based on the use of a screen printed carbon electrode modified with palladium nanoparticles and an amino-functionalized metal-organic framework. The morphology and properties of the resulting material were examined by X-ray photoelectron spectroscopy, X-ray diffraction, thermogravimetry, FTIR spectroscopy and transmission electron microscopy. Nitrite was chosen as a model analyte to evaluate the electron transfer performance of the modified SPCE. Its preparation conditions were optimized. The response to nitrite was studied via cyclic voltammetry, linear sweep voltammetry, and square wave voltammetry. Under the optimal conditions, the oxidation current (typically measured at -0.86 V vs Ag/AgCl) increases linearly in the 5 to 150 nM nitrite concentration range, and the detection limit is 1.3 nM. The sensor was applied to the detection of nitrite in (spiked) sausage and pickle samples. It is highly selective to nitrite in the presence of high concentrations of other electro-active compounds, stable, and well reproducible. In our perception, the sensor presented here reveals the large potential of MOF-based hybrid materials for use as an electrode material.
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Collections - College of Engineering > Department of Energy and Materials Engineering > 1. Journal Articles

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