Flexible Screen-Printed Electrochemical Sensors Functionalized with Electrodeposited Copper for Nitrate Detection in Water

A K M S Inam; Martina A Costa Angeli; Bajramshahe Shkodra; Ali Douaki; Enrico Avancini; Luca Magagnin; Luisa Petti; Paolo Lugli

doi:10.1021/acsomega.1c04296

Flexible Screen-Printed Electrochemical Sensors Functionalized with Electrodeposited Copper for Nitrate Detection in Water

ACS Omega. 2021 Dec 1;6(49):33523-33532. doi: 10.1021/acsomega.1c04296. eCollection 2021 Dec 14.

Authors

A K M S Inam^{1

2}, Martina A Costa Angeli¹, Bajramshahe Shkodra¹, Ali Douaki¹, Enrico Avancini¹, Luca Magagnin³, Luisa Petti¹, Paolo Lugli¹

Affiliations

¹ Faculty of Science and Technology, Free University of Bozen-Bolzano, Bolzano 39100, Italy.
² Department of Nutrition and Food Engineering, Daffodil International University, Dhaka 1207, Bangladesh.
³ Department of Chemistry, Materials and Chemical Engineering "Giulio Natta", Politecnico di Milano, Milano 20133, Italy.

Abstract

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^-, SO₄ ^2-, 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.