Abstract

We report here the preparation and characterization of polyaniline Ni-complex catalytic electrode by one-pot plasma deposition for the electrochemical detection of phosphate via the redox reaction of glucose. We first prepared a precursory solution by combining NiCl2 and 3-aminobenzoic acid in a mixed solution of methanol (MeOH) and water, and adding aniline as a conductive polymeric precursor for increasing the electron transfer potential. We then synthesized the catalytic electrode in a one-step cold plasma process by preparing the precursors on ITO glass. We characterized the obtained Ni-coordinate catalytic electrode via X-ray photoelectron spectroscopy (XPS), field emission scanning electron microscopy (SEM), and electrochemical methods. Electrochemical characterization produced stable redox properties of Ni3+/Ni2+ couples in a 0.1 M NaOH solution. Cyclic voltametric experiments have drastically increased electrocatalytic oxidation and reduction of glucose by increasing the concentration of phosphate (PO43−) ions using the prepared Ni-modified catalytic electrodes. From these results, the prepared catalytic electrode could be used as the electrochemical sensor for phosphate in actual water.

Highlights

  • Quantitative evaluation of phosphates, both of inorganic compounds and organic compounds, is important in biomedical research, biological diagnosis, and environmental monitoring [1,2,3]

  • We found that a polyaniline Ni-complex catalytic electrode can be applied as an electrochemical oxidation for glucose in the presence of high concentrations of phosphate

  • By examining the water contact angles, we determined that the contact angle of the bare indium tin oxide (ITO) electrode, No 1 was 77◦ and the contact angles of the polyaniline Ni-coordinated catalytic electrodes, No 2, No 3, and No 4 were 60◦, 53◦, and 51◦, respectively, at room temperature

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Summary

Introduction

Quantitative evaluation of phosphates, both of inorganic compounds and organic compounds, is important in biomedical research, biological diagnosis, and environmental monitoring [1,2,3]. The sensing range of phosphorus is between 0.2 in 10 mg/L in natural and waste waters and between 0.2 and 50 mg/kg in soil. A maximum permissible concentration of phosphate in river water is 0.32 μM and ranges between 0.0143 and 0.143 mM in wastewater [4]. The concentration of phosphate ions in human saliva is variable, ranging from between 5 and 14 mM [5]. Adult human serum with a range of 0.81 to 1.45 mM PO43− was used [6]. Many researchers have developed various detection methods for phosphate such as phosphate ion selective electrodes [7], chromatography [8], spectroscopy [9], and the development of sensors exploiting enzymatic reactions [10,11]. Little has been reported about electrochemical detection, which is known as a simpler method those described above

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