The largest database of trusted experimental protocols

43 protocols using sp 150 potentiostat

1

ZnO-V2O5 Coated PET Fiber Electrochemical Sensor

Check if the same lab product or an alternative is used in the 5 most similar protocols
All the electrochemical measurements were carried out using Biologic (SP-150) Potentiostat. The ZnO-V2O5 coated PET fiber was used as a working electrode, Ag/AgCl electrode in 0.2 M KCl as a reference electrode, and a Pt wire electrode as a counter electrode with different concentrations of NaOH and HCl as electrolytes. Prior to the electrochemical test, an electrode was prepared by thoroughly mixing active material (ZnO/V2O5), carbon black, and PVDF in a mass ratio of 80:10:10. The prepared sample was coated on the ZnO seed layered PET fiber using a dip coater. The fabricated electrode was dried in a vacuum oven at 60 °C and finally used as an electrochemical sensor.
+ Open protocol
+ Expand
2

Electrochemical Synthesis of Drug-Loaded Polypyrrole Films

Check if the same lab product or an alternative is used in the 5 most similar protocols
Drug containing PPy films were grown potentiostatically onto the device electrodes using a Bio-Logic SP-150 potentiostat. The dexamethasone electrosynthesis solution consisted of 0.2 M Pyrrole (Alfa Aesar, Ward Hill, MA) and 0.02 M dexamethasone 21 phosphate disodium salt (Sigma-Aldrich, used as received) in Milli-Q water of 18 MΩ/cm resistivity. The Indomethacine electrosynthesis solution consisted of 0.2 M Pyrrole and 0.01 M Indomethacin (Sigma-Aldrich) in acetonitrile. The acetylsalicylic acid electrosynthesis solution consisted of 0.2 M Pyrrole (Alfa Aesar, Ward Hill, MA) and 0.02 M acetylsalicylic acid (Sigma-Aldrich,) in Milli-Q water. The films were synthesized by applying a constant current of 0.1 mA for Indomethacin and 1 mA for acetylsalicylic acid and dexamethasone each for 10 minutes between the drug release electrode and the counter electrode. For drug release experiments, the counter and working electrodes were reversed. The amount of released DEX, ASA and Indomethacin was quantified by absorbance at 242 nm, 298 nm and 318 nm, respectively using an infinite M200 Pro plate reader (TECAN).
+ Open protocol
+ Expand
3

Conductivity Measurement of Ionic Liquids

Check if the same lab product or an alternative is used in the 5 most similar protocols
Specific conductivities of the pure ionic liquid and binary solutions with lithium salts were obtained by impedance spectroscopy using a sealed commercial conductivity probe (WTW, Weilheim, Germany) consisting of two rectangular platinized platinum electrodes fused into glass with a nominal cell constant of 0.5 cm−1. The actual cell constant was determined prior to the experiments using commercial conductivity standards. The impedance spectra were obtained with an SP-150 potentiostat (Biologic, Seysinnet-Pariset, France) by applying voltages of 5, 10 and 15 mV and frequencies from 200 kHz to 1 Hz in 50 logarithmic steps. The electrolyte resistance for the three voltages was averaged. Temperature was controlled by immersing the conductivity probe in a Proline RP 1845 thermostat (LAUDA, Lauda-Königshofen, Germany). The specific conductivity κ was calculated as the actual cell constant divided by the electrolyte resistance R . From the specific conductivity and density, the molar conductivity was calculated using Equation (5), with M the molar mass of the sample.
ΛM=κ Mρ.
+ Open protocol
+ Expand
4

Characterization of Dye-Sensitized Solar Cells

Check if the same lab product or an alternative is used in the 5 most similar protocols
The optical absorbance spectra were recorded using Shimadzu 1800 scanning double beam UV–Visible spectrophotometer. The structural properties of the dye coated films were studied by fourier transform infrared spectroscopy (Thermo Scientific™ Nicolet™ iS5 FTIR spectrometer) and atomic force microscopy (AFM-Park XE7, in 1 × 1 µm scan area). pH of the prepared dye solutions was measured using Eutech pH 700 m. The photovoltaic performance of the fabricated devices with effective area of 0.25 cm2 was studied using Keithley-2400 source measurement unit under simulated irradiation by 150 W Xe lamp with an intensity of 100 mWcm−2 and AM 1.5 filter (Peccell-PEC-L12, Kanagawa, Japan). All electrochemical studies were carried out using Bio Logic SP-150 potentiostat.
+ Open protocol
+ Expand
5

Electrochemical Synthesis and Drug Release of PPy/DEX Films

Check if the same lab product or an alternative is used in the 5 most similar protocols
PPy/DEX films were grown potentiostatically onto the device electrodes using a Bio-Logic SP-150 potentiostat. The electrosynthesis solution consisted of 0.2 M Pyrrole (Alfa Aesar, Ward Hill, MA) and 0.1 M DEX (Sigma-Aldrich, DEXamethasone 21 phosphate disodium, used as received) in Milli-Q water of 18 MΩ/cm resistivity. The film was synthesized by applying a constant potential of 1 V for 10 min between the device and a counter electrode. For drug release experiments, the counter and working electrodes were reversed. The amount of released DEX was quantified by absorbance at 242 nm (a characteristic band of DEX) using an infinite M200 Pro plate reader (TECAN).
+ Open protocol
+ Expand
6

Cyclic Voltammetry in Organic Solvent

Check if the same lab product or an alternative is used in the 5 most similar protocols
CV was performed using a BIOLOGIC SP‐150 potentiostat with positive feedback compensation in 0.10 m Bu4NPF6/CH2Cl2 (HPLC grade). Experiments were carried out in a one‐compartment cell equipped with a platinum working electrode (2 mm diameter) and a platinum wire counter electrode. A silver wire immersed in a 0.01 m solution of AgNO3 in CH3CN was used as reference electrode and checked against the ferrocene/ferrocenium couple (Fc/Fc+) before and after each experiment. The potentials were then expressed vs. Fc/Fc+.
+ Open protocol
+ Expand
7

Electrochemical Characterization Setup

Check if the same lab product or an alternative is used in the 5 most similar protocols
Electrochemical
studies were performed in a three-electrode configuration (unless
otherwise stated) using either a CH Instruments CHI600D potentiostat
or a BioLogic SP-150 potentiostat. A glassy carbon button electrode
(surface area = 0.071 cm2) or carbon felt was used as the
working electrodes (as specified), a Pt wire or a piece of carbon
felt was used as the counter electrode (as specified), and an Ag/AgCl
(NaCl, 3 M) reference electrode was used when specified. Glassy carbon
working electrodes were polished using polishing powder and then washed
with acetone and deionized water prior to use. Carbon felt electrodes
were not reused.
+ Open protocol
+ Expand
8

Cyclic Voltammetry Analysis of Redox-Active Materials

Check if the same lab product or an alternative is used in the 5 most similar protocols
Cyclic voltammetry measurements were performed using a three-electrode configuration composed of a glassy carbon working electrode, a Pt counter electrode and an Ag/AgCl reference electrode at around 25 °C. The electrolytes were prepared by dissolving redox-active materials (1 mmol) in aqueous KCl solution (1 M, 10 mL), using trace amount of aqueous KOH solution (1 M) to adjust pH to 9.0) Cyclic voltammogram of K4Fe(CN)6 and 2,6-DPPAQ were collected using a Biologic SP-150 potentiostat at a scan rate of 100 mV s−1 as shown in Supplementary Fig. 29. The crossover rates of 2,6-DPPAQ through membrane separators to catholytes, and K4Fe(CN)6 to analytes in the operating battery were measured by cyclic voltammetry.
+ Open protocol
+ Expand
9

Photocatalytic Electrode Fabrication and Characterization

Check if the same lab product or an alternative is used in the 5 most similar protocols
The photocatalyst powder was dispersed in H2O to form a 10 mg mL−1 solution under sonication for 30 min. Indium-tin oxide (ITO) glass, as the working electrode, was cleaned by sonication in cleanout fluid, acetone and ethanol for 10 min. The as-prepared solution was dropped onto the pretreated ITO surface and allowed to dry under vacuum conditions for 24 h at 60 °C. Subsequently, the uncoated part of the ITO glass was isolated with epoxy resin. The photocurrent was measured by an electrochemical analyzer (CHI660D Instruments) in a conventional three-electrode electrochemical cell with the working electrode, a platinum foil counter electrode and Ag/AgCl (3 M KCl) as reference electrode. A 300 W Xenon lamp with 400 nm cutoff filter was utilized as a light source. A 0.5 M Na2SO4 aqueous solution was used as the electrolyte. The Mott–Schottky measurements were carried out using a Bio-Logic SP-150 potentiostat equipped with a VMP3B-20 20A booster.
+ Open protocol
+ Expand
10

Electrochemical Impedance Spectroscopy for Biomolecular Detection

Check if the same lab product or an alternative is used in the 5 most similar protocols
An SP-150 potentiostat (Bio-Logic, USA) was used for EIS analysis. EIS analysis was performed to distinguish between antibodies and antigens and Aβ(1–42) monomers and oligomers via the measurement of impedance differences. Figure 3 shows the schematic illustration of the experimental setup. The surface-modified nanostructured biosensor was used as the working electrode in electrochemical analysis, and Pt film and Ag/AgCl/3 M KCl functioned as the counter and reference electrodes, respectively. A solution of 5 mM Fe(CN)64−, 5 mM Fe(CN)63−, and 0.1 M KCl in 100 mM MES (pH = 6.0) was used as the electrolyte solution. The applied AC power amplitude was 10 mV. The scanning AC frequency was between 0.02 Hz and 200 kHz.
+ Open protocol
+ Expand

About PubCompare

Our mission is to provide scientists with the largest repository of trustworthy protocols and intelligent analytical tools, thereby offering them extensive information to design robust protocols aimed at minimizing the risk of failures.

We believe that the most crucial aspect is to grant scientists access to a wide range of reliable sources and new useful tools that surpass human capabilities.

However, we trust in allowing scientists to determine how to construct their own protocols based on this information, as they are the experts in their field.

Ready to get started?

Sign up for free.
Registration takes 20 seconds.
Available from any computer
No download required

Sign up now

Revolutionizing how scientists
search and build protocols!