Flexible Screen-Printed Electrochemical Sensors Functionalized with Electrodeposited Copper for Nitrate Detection in Water
Autor: | Inam, A. K. M. S., Costa Angeli, M. A., Shkodra, B., Douaki, A., Avancini, E., Magagnin, L., Petti, L., Lugli, P. |
---|---|
Jazyk: | angličtina |
Rok vydání: | 2021 |
Předmět: | |
Zdroj: | ACS Omega, Vol 6, Iss 49, Pp 33523-33532 (2021) ACS Omega |
ISSN: | 2470-1343 |
Popis: | Nitrate (NO3–) contamination is becoming a major concern due to the negative effects of an excessive NO3– presence in water which can have detrimental effects on human health. Sensitive, real-time, low-cost, and portable measurement systems able to detect extremely low concentrations of NO3– in water are thus becoming extremely important. In this work, we present a novel method to realize a low-cost and easy to fabricate amperometric sensor capable of detecting small concentrations of NO3– in real water samples. The novel fabrication technique combines printing of a silver (Ag) working electrode with subsequent modification of the electrode with electrodeposited copper (Cu) nanoclusters. The process was tuned in order to reach optimized sensor response, with a high catalytic activity toward electroreduction of NO3– (sensitivity: 19.578 μA/mM), as well as a low limit of detection (LOD: 0.207 nM or 0.012 μg/L) and a good dynamic linear concentration range (0.05 to 5 mM or 31 to 310 mg/L). The sensors were tested against possible interference analytes (NO2–, Cl–, SO42–, HCO3–, CH3COO–, Fe2+, Fe3+, Mn2+, Na+, and Cu2+) yielding only negligible effects [maximum standard deviation (SD) was 3.9 μA]. The proposed sensors were also used to detect NO3– in real samples, including tap and river water, through the standard addition method, and the results were compared with the outcomes of high-performance liquid chromatography (HPLC). Temperature stability (maximum SD 3.09 μA), stability over time (maximum SD 3.69 μA), reproducibility (maximum SD 3.20 μA), and repeatability (maximum two-time useable) of this sensor were also investigated. |
Databáze: | OpenAIRE |
Externí odkaz: |