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%).
Pgstat204
The PGSTAT204 is a potentiostat/galvanostat from Metrohm, a leading manufacturer of lab equipment. The device is designed for electrochemical measurements and analysis. It provides precise control and measurement of electrical signals in various electrochemical applications.
Lab products found in correlation
64 protocols using pgstat204
Electrochemical and Spectroscopic Analysis of PB@CNT-PPy Nanocomposite
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%).
Electrochemical Characterization of AuNP-Modified Electrodes
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.
Photoelectrochemical Characterization Workflow
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).
Characterization of Graphene Oxide and Polyethyleneimine-Reduced Graphene Oxide Films
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).
Electrochemical Fabrication of MIP Sensors
Electrochemical Detection of L-Cysteine and SARS-CoV-2 Spike Protein
Electrochemical Corrosion Monitoring of Steel in Concrete
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 (RΩ) 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.
Electrochemical Characterization of Ferricyanide Redox Probe
Cyclic Voltammetry of Dy Complex
Graphene Electrode Fabrication and H2S Sensing
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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