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64 protocols using pgstat204

1

Electrochemical and Spectroscopic Analysis of PB@CNT-PPy Nanocomposite

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Electrochemical studies were performed using an Autolab PGSTAT204 analysis system with Nova 2.1.1 software from Eco Chemie (Utrecht, NLD). All measurements were made using a three-electrode system comprised of SPE as the working electrode, a helical platinum wire as an auxiliary electrode, and an Ag/AgCl (KCl sat) electrode as reference. All potentials given in this work were determined relative to the Ag/AgCl (KCl sat) reference electrode.
Chemical characterization of the PB@CNT-PPy nanocomposite was performed by Fourier transform infrared (FT-IR) spectroscopy analyses. FT-IR spectra were recorded on a Bruker FT-IR spectrometer, Model IFS-66 (Ettlingen, DEU, Germany), controlled by OPUS software (version 6.5). The measurements were made in the attenuated total reflectance (ATR) mode with a frequency resolution of 25 cm−1 at room temperature (24 °C) and controlled humidity (~10%).
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2

Electrochemical Characterization of AuNP-Modified Electrodes

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All the electrochemical
measurements, including CV and EIS, were performed by an Autolab PGSTAT204
potentiostat/galvanostat (Ecochemie) setup interfaced to a computer
controlled by the NOVA 1.11 software package. The polished bare GC
electrode, control, or AuNP-modified GC electrode acted as the working
electrode, a platinum electrode as the counter electrode, and a saturated
calomel electrode (SCE) as the reference electrode. All the electrochemical
experiments were carried out at room temperature in a Faradaic cage.
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3

Photoelectrochemical Characterization Workflow

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The active surface of the photoelectrode
was exposed to PBS electrolyte (0.01 M phosphate buffer, 0.137 M NaCl).
By mounting the photoelectrode in a dedicated measurement cell, only
the semiconducting layer is exposed to the electrolyte (through a
1 cm diameter mask), while the buried ITO surface and the electrical
contacts remain separated via a polydimethylsiloxane
O-ring. The measurement cell allows the exposition to the illumination
from either the ITO side or the solution side, the latter through
a quartz window. In a three-electrode setup, the photoelectrode was
operated as the WE. An Ag|AgCl (3 M KCl) RE was used in combination
with a Pt CE. The light source was a monochromatic LED (Thorlabs M530L4)
driven by a source-measure unit (Thorlabs DC2200). A potentiostat
(Metrohm PGSTAT204) was used to set the voltage and collect the current.
The potentiostat was also used for impedance spectroscopy measurements.
Results are shown as mean ± standard deviation (n = 3 samples).
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4

Characterization of Graphene Oxide and Polyethyleneimine-Reduced Graphene Oxide Films

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Raman spectroscopy (300R,
WITec, Germany) and FTIR–ATR (VARIAN 670/620, CA, USA) were
used to characterize the GO and PEI–rGO thin film. UV–vis
spectra were recorded using a liquid spectrophotometer (UV–vis–NIR;
Cary 5000, Agilent, USA). A field-emission scanning electron microscope
(S-4800, Hitachi, Japan) was used to image the PEI–rGO thin
films on ITO/glass electrodes. The samples were coated with platinum
by ion sputtering (E-1045, Hitachi, Japan). The chemical bonding of
the synthesized GO and PEI–rGO thin films was studied by XPS
(K-Alpha, Thermo Scientific, USA). The synthesized GO and PEI–rGO
sheets were also characterized using a tapping mode atomic force microscope
(Bruker Instrument, USA). All electrochemical measurements were recorded
using an Autolab System (PGSTAT204, Metrohm, Netherlands) controlled
by the NOVA 1.10 software at room temperature (23 ± 2 °C).
All the measurements (otherwise mentioned) were performed in 5 mM
[Fe(CN)6]3–/4– and 0.5 M KCl (1×
PBS, pH 7.4) with a three-electrode system comprising a working electrode
(ITO/glass; [2 cm × 0.5]), a reference electrode (Ag/AgCl), and
a counter electrode (Pt).
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5

Electrochemical Fabrication of MIP Sensors

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Electrochemical measurements were performed using an Autolab potentiostat (PGSTAT 204, Metrohm). Platinum (Pt) interdigitated microelectrodes, obtained by standard lithography fabrication, composed of two Pt connection tracks and patterned on a glass substrate were used as working and counter electrodes, while an Ag/AgCl electrode was used as the reference. All measurements were performed at room temperature (22 °C). potential range -0.2-0.8 V vs. Ag/AgCl at a scan rate of 50 mV s -1 in a solution of acetate buffer (0.5 M, pH 5.2) containing 0.1 mg mL -1 o-PD. Before polymerization, TGF-β1 was added in the o-PD solution as a template molecule at a concentration of 1 µg mL -1 . After polymerization, the modified electrode was washed with different solutions to explore the best conditions for the template removal. The electrochemical stepwise process of MIP fabrication was investigated by the Differential Pulse Voltammetry (DPV) technique in the potential range of -0.2-0.8 V at a scan rate of 100 mV s -1 . The control electrode was modified with a non-imprinted polymer (NIP), without TGF-β1 being added as a template. Modified electrodes were stored at room temperature (22 °C).
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6

Electrochemical Detection of L-Cysteine and SARS-CoV-2 Spike Protein

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All electrochemical measurements were performed in an AutoLab PGSTAT204 potentiostat/galvanostat with an impedance module FRA32M managed by NOVA 2.1.4 software (Metrohm, Utrecht, Netherlands). Cyclic voltammetry (CV) measurements were performed from 0.0 to +1.2 V, at a scan rate of 50 mV s−1, and chronoamperometry measurements at an applied potential of +0.55 V were used for the determination of L-cysteine. On the other hand, electrochemical impedance spectroscopy (EIS) was recorded from 100 kHz to 0.10 Hz, with an amplitude of 10 mV, and square wave voltammetry (SWV) measurements were performed with an amplitude of 80 mV, a frequency of 80 Hz, and a step potential of 10 mV. EIS and SWV were applied for the detection of the SARS-CoV-2 spike protein. For these analyses, 0.10 mol L−1 KCl (pH 7.0) was used as a supporting electrolyte, and an equimolar mixture of 5.0 mmol L−1 [Fe(CN)6]3−/4− was applied as a redox probe. The EIS measurements were calibrated by normalized impedance change (NIC%) [43 (link),44 (link)] concerning the control. The NIC% value was calculated using Equation (1), where, in this case, Zcontrol is the magnitude of charge transfer resistance (Rct) for a control sample without the antigen, and Zsample is the magnitude of Rct for each added point of concentration of the antigen.
NIC%=ZsampleZcontrolZcontrol×100      
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7

Electrochemical Corrosion Monitoring of Steel in Concrete

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The oxygen concentration in the glovebox atmosphere was less than 1% throughout the experiment. Such a low oxygen content was verified with chronoamperometric readings at potentials of −750 mVAg/AgCl and −850 mVAg/AgCl [16 (link)]. The results (Figure 2) showed that the oxygen content was negligible, for negative current density values are associated with oxygen reduction whilst values near zero are indicative of an inert atmosphere and those above zero of anodic behaviour in the steel.
Three techniques were deployed to assess specimen electrochemical behaviour: linear polarisation resistance (LPR); electrochemical impedance spectroscopy (EIS); and chronopotentiometry (CP). All three measure the open circuit corrosion potential (OCP) and polarisation resistance (Rp) values from which corrosion rate can be calculated. The EIS and CP findings can also be used to determine the resistance drop (R) value. All the readings were recorded on a Metrohm Autolab PGSTAT204 potentiostat/galvanostat. In the electrochemical cell used, saturated concrete was the medium, a steel bar the working electrode, stainless steel mesh the auxiliary electrode, and saturated Ag/AgCl solution the reference electrode. The electrochemical readings were logged over 232 days on duplicate samples.
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8

Electrochemical Characterization of Ferricyanide Redox Probe

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All the reagents used in this study were of analytical grade, obtained from Fisher (Hampton, VA, USA), Dinâmica (Indaiatuba, Brazil), Sigma-Aldrich (St. Luis, MO, USA), or Fluka (Buchs, Switzerland) and the solutions were prepared using purified water Heal Force® (resistivity ≥ 18.2 MΩ cm). The electrochemical measurements (cyclic voltammetry (CV), open circuit potential (OCP), and square wave voltammetry (SWV)) were performed, using a potentiostat/galvanostat PGSTAT204 (Metrohm Autolab, Utrecht, The Netherlands) managed by Nova 2.1.5 software (Metrohm Autolab, Utrecht, The Netherlands, available for free download). Cyclic voltammograms were achieved using a 0.1 mmol L−1 ferricyanide potassium and 0.1 mol L−1 KCl solution (both obtained from Sigma-Aldrich®, St. Luis, MO, USA), as a redox probe and supporting electrolyte, respectively.
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9

Cyclic Voltammetry of Dy Complex

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All cyclic voltammetry experiments were conducted under inert atmosphere in an argon-filled glovebox. Complex 2-Dy was measured using a PGSTAT204 from Metrohm with 1.3 mmol L−1 sample solution in THF with (nBu4N)(PF6) as supporting electrolyte (0.25 mol L−1) in conjunction with a glassy carbon working electrode, a Pt spring counter electrode and a Pt wire pseudo reference electrode. All voltammograms were externally referenced to a ferrocene solution with identical supporting electrolyte concentration.
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10

Graphene Electrode Fabrication and H2S Sensing

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A DIW digital material depositor (DMD100
from Kellenn Technologies, FR) was used for the fabrication of bare
Gr electrodes.
The printed devices were morphologically characterized
by means of a digital microscope (AM4815ZTL from DinoLite, NE) and
a field emission-scanning electron microscope (MerlinFE-SEM from Carl
Zeiss, GE) with an energy-dispersive X-ray spectroscopy (EDX) analysis
system. Electrochemical performance was tested by using a potentiostat
μAutolab (PGSTAT204 from Metrohm Autolab BV, NE). Stock solutions
of H2S were standardized using a commercial S2– ion-selective electrode (Thermo Scientific Orion Star, USA) coupled
to a pH/ISE SB90M5 measurement system (SympHony, USA).
Real
samples were compared to a SULF-10 commercial H2S gas sensor
coupled to a X-5 UNIAMP multimeter both from Unisense,
DK.
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