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Electrochemical workstation

Manufactured by Metrohm
Sourced in Switzerland

The Electrochemical Workstation is a versatile instrument designed for a wide range of electrochemical measurements and experiments. It provides advanced capabilities for controlling and monitoring electrochemical processes, enabling researchers and analysts to investigate various electrochemical phenomena.

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4 protocols using electrochemical workstation

1

Synthesis and Characterization of H3L Ligand

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The ligand 5-(5-carboxy-pyridin-3-yloxy)-isophthalic
acid (H3L) was purchased from Jinan Henghua Technology
Co. Ltd. All other reagents were purchased commercially and used as
received without further purification. Elemental analysis was performed
by an Elementar Vario ELIII instrument. The powder X-ray diffraction
(PXRD) was obtained from a Rigaku X-ray diffractometer (Cu Kα,
λ = 1.5418 Å). Infrared spectrum (IR) was measured in the
range ν = 400–4000 cm–1 using KBr pellets
by Thermo Scientific FTIR-Nicolet iS10. Thermogravimetric analysis
(TGA) was conducted on a Metler-Toledo synchronous differential thermal
analyzer under N2 atmosphere and the test range from 25
to 800 °C at the heating rate of 10 °C min–1. Magnetic susceptibility χM was investigated between
2 and 300 K under 1000 Oe magnetic field using a SQUID magnetometer
(Quantum MPMS). The alternating current (AC) impedance spectra were
measured on a Metrohm Autolab Electrochemical workstation using a
quasi-four-probe method (frequencies: 1 Hz to 1 MHz; ac voltage amplitude:
0.01 V).
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2

Electrochemical Characterization of CoOx-rGO

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To perform the electrochemical measurements, an electrochemical workstation (Metrohm Autolab B.V., Utrecht, The Netherlands) was used with a three-electrode configuration, where the as-prepared CoOx-rGO, Hg/HgO and Pt wire were working, reference and counter electrodes, respectively. The electrochemical measurements included the cyclic voltammetry (CV), galvanostatic charge–discharge test (GCD) and electrochemical impedance spectroscopy (EIS). CV measurements were performed at different scan rates from 10 to 100 mV/s in the potential window of 0–0.6 V. The GCD tests were carried out in the same potential window and at various applied current densities. The EIS measurements were recorded in a frequency range of 100 kHz to 10 mHz with an ac perturbation signal of 10 mV. All the electrochemical measurements were carried out in 1 M KOH aqueous electrolyte in ambient conditions at room temperature (23 °C). The electrochemical measurements setup was constructed using the PTFE (Teflon) rod (McMaster-Carr, Elmhurst, IL, USA), and it is schematically shown in Figure 2.
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3

Differential Pulse Voltammetric Measurements

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Differential pulse voltammetric (DPV) measurements were carried out on an Autolab Electrochemical Workstation (Metrohm, Switzerland) with a conventional three-electrode system: an ITO electrode as the working electrode, a platinum wire as the counter electrode, and an Ag/AgCl electrode as the reference electrode. It should be noted that ITO electrode with negative charge was obtained by using a previously reported pretreatment method29 (link).
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4

Catalyst Ink Preparation and Electrochemical Evaluation

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The catalyst ink was prepared by adding the catalyst (0.5 mg) and the Nafion solution (10 μL) into an iPA and water (1 : 1) mixture (500 μL). Then, the catalyst suspension (11–13 μL) was dropcast on a clean glassy carbon (GC) disk electrode having a 5 mm diameter (geometric area = 0.196 cm2) and dried under an infrared (IR) lamp. The electrocatalytic activities of the different catalysts were tested on an Autolab electrochemical workstation (Metrohm, 302N) in a standard three electrode system. Ag/AgCl saturated with 3 M KCl and a Pt wire were used as the reference and counter electrodes, respectively. A rotating disc electrode (RDE) of the catalyst deposited GC was used as the working electrode.
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