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Leo 1550 fe sem

Manufactured by Zeiss
Sourced in United Kingdom

The LEO 1550 FE-SEM is a field emission scanning electron microscope (FE-SEM) produced by Zeiss. It provides high-resolution imaging of a wide range of materials and samples. The FE-SEM utilizes a field emission source to produce a focused electron beam, enabling detailed observation and analysis at the nanoscale level.

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5 protocols using leo 1550 fe sem

1

Comprehensive Characterization of Carbon Materials

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The morphology characterization of the samples were performed by scanning electron microscopy (SEM) using a ZEISS LEO 1550 FE-SEM at an accelerating voltage of 7 kV. For the HRTEM analysis, the samples were scratched onto lacey carbon grids and observed using a JEOL 2010F at the Canadian Centre for Electron Microscopy (Hamilton, Ontario, Canada). The surface chemical composition analysis was performed by X-ray photoelectron spectroscopy (XPS) analysis using a multi-technique ultra-high vacuum imaging XPS microprobe spectrometer (Thermo VG Scientific ESCALab 250) with a monochromatic Al-Ka 1486.6 eV X-ray source. Raman analysis was performed with a 50x objective, and the spectra were acquired with a laser wavelength of 633 nm at a power of 0.1 mW. For the electrochemical oxidation, a Gamry Potentiostat (Series 300) was employed. The electrical measurements of the carbon-based devices were performed with a Keithley 2602 A source meter at ambient conditions.
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2

Synthesis of Functionalized Silica Particles

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Monodisperse silica (Si) particles with a diameter of 2–3 μm were synthesized using tetraethyl orthosilicate (TEOS), 29% ammonia and 100% ethanol via the Stöber method. To produce a positively charged surface, Si particles were suspended in ethanol containing 1 mg/ml 3-aminopropyl triethoxysilane (APTES) and stirred overnight. To prepare FITC-labeled Si particles, FITC was first reacted with APTES in the presence of ethanol and ammonia. Afterwards, TEOS was added to FITC dye solution and stirred overnight to form FITC-labeled Si particles. All synthesized Si particles were washed three times with 100% ethanol followed by three times with TBS to remove free substrate. Particles were characterized with dynamic light scattering using a Zetasizer (Malvern Instruments, Malvern, Worcestershire, UK) and LEO 1550 FE-SEM (Zeiss, Atlanta, GA, USA) prior to PMDV coating.
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3

Fracture Surface Roughness Characterization

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After the mechanical data were obtained, the roughness of the fracture areas (Ra) of all AD, BDS, VV, WDD, C1, and C2 specimens was measured using a contact profilometer (Taylor Hobson Form TalySurf Serie 2 FTS S2, Leicester, UK). Since WNc and WNu both used the same resin, the fracture surface measurements were performed only on the WNc group, but the results may be considered to apply to both WN groups. The roughness parameter Ra stands for “roughness average”. It is the most common parameter for describing a surface’s roughness and is defined as the arithmetic mean of the absolute values of the roughness profile ordinates. The measurements were performed perpendicular to the surface. The profilometer filter settings were chosen according to the respective ISO norm [21 ]. Three standardised measurements of 4.0 mm were performed. The cut-off wavelength was set at λ = 0.8 mm, meaning that roughness peaks larger than 0.8 mm did not contribute to the result.
To gain a better understanding of the specific fracture surface configurations, scanning electron microscope (SEM) images were produced using a LEO-1550 FE-SEM (Carl Zeiss GmbH, Vienna, Austria) at magnifications of 100-fold and 450-fold.
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4

Scanning Electron Microscopy of Samples

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Samples were removed from culture, washed with PBS and fixed using 2.5% (w/v) glutaraldehyde for 15 min at room temperature, washed with PBS and submerged in 70% ethanol for 15 min, then 90% ethanol for 15 min followed by two changes of 100% ethanol for 15 min. Samples were dried using a critical point dryer (Prion, UK). Dry samples were fixed to SEM stubs (Agar Scientific, UK) using double-sided carbon sticky tabs (Agar Scientific, UK). The samples were then coated with 20 nm of chromium using a sputter coater (Emtech, UK). The samples were observed under a Leo 1550 FESEM (Zeiss, UK). This was repeated 3 times for each time point. Representative images were used in results section. Where nodule formation was observed, measurements were taken using the annotation function on the LEO SEM software (Zeiss, Germany).
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5

High-Resolution Scanning Electron Microscopy

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Scanning electron microscopy was performed using a Zeiss LEO 1550 FE-SEM with a field emission source operating at 2 kV acceleration voltage in the In-Lens mode.
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