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Versastat 4 potentiostat galvanostat

Manufactured by Ametek
Sourced in United States

The VersaSTAT 4 is a potentiostat/galvanostat designed for electrochemical measurements. It provides precise control and measurement of voltage, current, and impedance parameters.

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6 protocols using versastat 4 potentiostat galvanostat

1

Characterization of Fabricated Electrodes

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The surface morphology, thickness, and the live quantitative colored images of the fabricated electrodes were obtained using Thermo-Fisher Scientific Apreo 2C scanning electron microscopy equipped with ColorSEM technology.
Thermogravimetric analysis to estimate the SAM surface coverage was done using a Q500 thermogravimetric analyzer (TA Instruments, DE, USA). The adsorption of proteins onto NPG was studied using a Varian Cary 50 UV–Visible spectrophotometer. UV–Vis spectra and absorbance readings were acquired using the Varian Cary 50 UV–Vis spectrophotometer. A Suprasil quartz spectrophotometer cuvette with a 10 mm light path and volume capacity of 1.0 mL (model number 14-385-902C, Fischer Scientific, Pittsburgh, PA, USA) was used for all experiments.
Electrodeposition and dealloying were carried out using an EG&G Princeton Applied Research 273A digital potentiostat/galvanostat and the PowerPULSE software. Cyclic voltammetry scans and reductive desorption studies were done using a VersaSTAT 4 potentiostat/galvanostat (Princeton Applied Research, AMETEK Scientific Instruments) and the VersaStudio software.
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2

3D Printed Electrochemical Deposition Setup

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The printing nozzles were 1.2 mm and 0.7 mm plastic pipettes, mounted on a 1 ml plastic syringe, which contained the electrolyte and the anode. This small syringe was connected to a larger syringe connected to a syringe pump (NE-300 New Era Pump). The nozzle was mounted on a z-stage, and the substrate was mounted on a xy-stage, and all stages were controlled using the same controller. G-code was used to control the nozzle path. A VersaSTAT-4 Potentiostat/Galvanostat (Princeton Applied Research) was used to apply the current/voltage.
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3

Cyclic Voltammetry and EIS Characterization of Aptamer Affinity

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VersaStat 4 potentiostat galvanostat (Princeton applied research, Ametek scientific instruments, Oak Ridge, TN, USA) controlled by VersaStat studio was used for all cyclic voltammetry (CV) sweeps. The working area (CE, WE, and RE) was covered with 50 µL of 1 mM [Fe (CN)6]3−/4− containing 0.1 M KCl + 3 mM Mg2+ (MgCl2) in PBS buffer, while the measurements were performed with a scan rate of 100 mV/s and a scan potential between −0.8 to 0.8 V. Electrochemical impedance spectroscopy (EIS) measurements were performed in a frequency range of 10 mHz–1 MHz, an AC amplitude of 50 mV and a sampling rate of 60 points using [Fe (CN)6]3−/4− as an electrolyte. The aptamers affinity values (Kd) values were also calculated by nonlinear regression analysis from the calibration curve (employing the Langmuir–Hill equation).
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4

Nanofilm-Pt Electrode Electrochemical Analysis

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Electrochemical measurements were performed at a CHI 660 E electrochemical workstation (CHI Instruments, Inc. USA). A threeelectrode system was employed with Ag/AgCl electrode as reference electrode, a platinum plate as counter electrode, and homemade nanofilm-Pt or NPt electrode (diameter, 3 mm) as working electrode. All the potentials in this work were with respect to Ag/ AgCl electrode and all measurements were carried out at room temperature (25 ± 2 C). EIS experimental was recorded using VersaSTAT 4 potentiostat/Galvanostat (Princeton Applied Research, AMETEK Inc, USA). The amplitude of modulation potential is 5 mV, and frequency range is from 10 5 to 10 À3 Hz. All measurements were carried out at room temperature (25 ± 2 C). Data analysis was performed with ZSimpWin 3.21 using the proposed equivalent circuit. Additionally, scanning electron microscopy (SEM) was obtained on a SU-70 (Hitachi) field emission scanning electron microanalysis at an operation potential of 5 kV.
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5

Glucose Sensing Microcapsule Electrochemistry

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Polyelectrolyte microcapsules, in the amount of 5 μL with incorporated GOx, were applied onto the surface of a Prussian blue electrode and dried at 22 °С for 30 min. Between measurements, the biosensors were stored at a temperature of 4 °С in the dark. The measurements were carried out at a temperature of 22 °С in a 1-ml cell at constant stirring. The measurements were performed on an IPC-Micro galvanopotentiostat (Kronas Ltd, Russia). Glucose solutions were prepared in a 25 mM sodium–potassium–phosphate buffer solution (pH 6.5) with the addition of 20 mM NaCl.
The voltammetric and impedance measurements were carried out with a VersaSTAT 4 potentiostat galvanostat (Ametek Inc., USA) in the same solution with the addition of 5 mM [Fe(CN)6]3. A scanning rate of 40 mV/s was used for voltammetric measurements. A 100 mV constant potential (40 kHz–0.02 Hz frequency range) and a voltage modulation of 10 mV were used to obtain impedance spectra. The correct equivalent circuit for every system was picked using ZSimpWin software (EChem Software, USA). The measurements were carried out with constant stirring of solutions.
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6

Electrochemical Performance of NiMoO4/NG Nanocomposite

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The electrochemical performance of NiMoO4/NG nanocomposite electrodes constructed with graphite foil current collectors was investigated in a three-electrode system. The reference and counter electrodes were calomel and platinum, respectively, and the electrolyte was 1.0 M KOH. Cyclic voltammetry (CV) was carried out at voltages of 0–0.7 V at scan rates of 5–100 mVs−1 using a VersaSTAT 4 Potentiostat Galvanostat (Ametek, Berwyn, PA, USA). Galvanostatic charge–discharge (GCD) tests were conducted at voltages of 0–0.5 V at various current densities. Electrochemical impedance spectroscopy measurements were performed over a frequency range of 0.01 Hz to 100 KHz at a voltage amplitude of 10 mV.
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