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Pp211

Manufactured by Zahner
Sourced in Germany

The PP211 is a laboratory equipment designed for precision mixing and blending of various materials. It features a compact and durable construction, allowing for efficient and consistent sample preparation. The core function of the PP211 is to thoroughly mix and homogenize samples, ensuring accurate and reproducible results.

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5 protocols using pp211

1

Characterization of Modified Electrodes

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The sheet resistance of modified electrodes was measured with Fluke Ohmmeter (1550B). Absorption measurements were taken with a single beam UV–Vis Spectrophotometer (CECIL CE9200) from 200 to 800 nm. Scanning electron microscopy (SEM) and atomic force microscopy (AFM) tests were done on prepared samples using (LEO 1455VP) and (Micro Photonics Inc/ Dual scope DS95-200E) instruments, respectively. A fluorescence spectrometer (PerkinElmer LS55) was used to measure the fluorescence intensity of tested samples. The cyclic voltammetry (CV) measurements were performed on electrodes using a (Zahner PP211 potentiostat) in the three-electrode electrochemical cell. In this test, the surface of prepared electrodes was used as a working electrode, and platinum was used as a counter electrode with Ag/AgCl as the reference one. A KCl solution (0.1molar in deionized water) was used as a standard electrolyte in all tests. In all of CV tests, the potential scan step was 0.005 V, and the potential scanning speed was 0.05 Vs−1. Each cyclic voltammogram presented in this research work is the most representative cycle obtained for each experiment.
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2

Electrochemical Cell Detachment for Cell Retrieval

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After cell capture, the washed CNF-Chip with cells was taken out and placed in an electrolytic cell with PBS as the electrolyte. The conductive CNF-Chip was taken as the working electrode, Ag/AgCl electrode was the reference electrode, and the platinum electrode was the counter electrode. A potential of −1.2 V was then applied by the electrochemical workstation (Zahner PP211) for 6 min. The cells were then released and collected by well plates. After that, the residual cells on the CNF-Chip were fixed with 2.5% glutaraldehyde for 30 min, stained with DAPI for 20 min, and observed under a fluorescence microscope. Five random fields of the sample were photographed. The obtained images were analyzed by ImageJ software, and the release efficiency ( ER ) was calculated according to Equation (3): ER%=(1NRNT×EC)×100%
where  NR is the number of residual cells on the CNF-Chip after release, NT is the total number of cells pumped in, and EC is the capture efficiency.
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3

SEM and Photoelectrochemical Analysis

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The scanning electron microscope (SEM) images were obtained by the field emission SEM (ZEISS, Germany). Photoelectrochemical (PEC) measurements were performed on an electrochemical workstation (Zahner Zennium PP211, Germany).
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4

Comprehensive Characterization of Nanomaterials

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SEM images were obtained from JSM-6700F microscope (JEOL, Japan). HRTEM image was recorded by JEM-2100F microscope (JEOL, Japan). FT-IR spectra were obtained with Perkin-Elmer 580B spectrophotometer (Perkin-Elmer, USA). XRD patterns were collected from D8 focus diffractometer (Bruker AXS, Germany). PEC tests were carried out on electrochemical work station (Zahner Zennium PP211, Germany). UV-vis measurements were obtained on Lambda 35 UV-vis spectrometer (Perkin-Elmer, USA). PL spectra were obtained on LS-45/55 PL spectrometer (Perkin-Elmer, USA).
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5

Photoelectrochemical Characterization of CoFe2O4

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Photoelectrochemical measurements were performed using a (Zahner Zennium, PP211) potentiostat with a three electrode cell assembly. Nanostructure film of CoFe2O4 was used as a photoanode, platinum wire as the counter electrode and Ag/AgCl (in sat. KCl, 3.6 M) was used as the reference electrode. A 0.1 M Na2S solution was used as an electrolyte solution. A tungsten halogen lamp of intensity ~100 mW/cm2 was used as a light source. Current-potential measurements were performed with a slew rate of 10 mV/s. Electrochemical impedance spectroscopy measurements were performed in the frequency range of 100 mHz to100 kHz. Voltage-capacitance measurements were performed at 1 kHz with an AC disturbance of 10 mV.
All experimentally measured potentials vs. Ag/AgCl were converted into reversible hydrogen electrode (RHE) scale using the equation; ERHE=EAg/AgCl+0.059pH+EAg/AgClo where, E(Ag/AgCl)o=0.1976 at 25 °C.
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