We introduce the fabrication and electrochemical application of platinum nanoflower-modified glassy carbon electrode (PtNFs/GCE) for the trace level determination of lead and cadmium using differential pulse anodic stripping voltammetry (DPASV). The modified electrodes have been characterized by EDX, XRD, SEM, and AFM techniques to confirm chemical and physical properties. The effect of potential electrodeposition on the properties of the electrode was investigated. At −0.2 V of potential, platinum developed with a nanoflower shape and dispersed densely all over the glassy carbon surface. In this condition, the highest of lead and cadmium electrochemical signals was clearly observed. The sensor showed wide linearity in the concentration range of 1–100 μg·L−1 with detection limits of 0.408 μg·L−1 and 0.453 μg·L−1 for lead and cadmium ions, respectively. The produced electrodes have good reproducibility with relative standard deviations of 4.65% for lead and 4.36% for cadmium ions. The results demonstrate that this simple, stable, and sensitive sensor is suitable for the simultaneous electrochemical determination of Pb2+ and Cd2+ at trace levels.
Platinum nanoflowers modified glassy carbon electrodes (PtNFs/GCE) was fabricated simply for lead determination in water samples. The modified electrodes were prepared by electrodeposition in hexachloroplatinic acid solution at constant potential. The influence of deposition time and potential on surface morphology, chemical composition, electrochemical properties of electrode were investigated. At À 0.2 V of potential and 150 s of deposition duration, platinum developed as nanoflower shape and scattered densely all over the glassy carbon surface, producing the largest electrochemically active surface areas. The highest differential pulse stripping voltammetry (DPSV) signal of lead was obtained by using the prepared electrode. Under optimized experimental condition of electrolyte, accumulation potential and time, the peak current was found to be linear proportion to lead concentration in range of 1 to 100 μg L À 1 (slope = 0.371) with a limit of detection of 0.398 μg L À 1 . The method has good repeatability and reproducibility with relative standard deviations of 1.47 % and 4.83 %, respectively. The modified PtNFs/GCE also demonstrated an excellent long-term stability with only 9 % decrease in Pb peak current over 30 days. Moreover, the performance of the modified PtNFs/GCE in determination of Pb(II) in two industrial wastewaters was good agreement with data obtained by a graphite furnace atomic absorption spectrometry (GFAAS) method.
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