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Feg250 microscope

Manufactured by Thermo Fisher Scientific

The FEG250 microscope is a field emission gun (FEG) scanning electron microscope (SEM) designed for high-resolution imaging and microanalysis of samples. It features a high-brightness electron source, advanced optics, and a range of detectors to provide detailed information about the surface morphology and elemental composition of specimens.

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2 protocols using feg250 microscope

1

Comprehensive Characterization of Novel Materials

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XRD measurements
were taken with a Stoe X-ray diffractometer using Cu Kα1 radiation (λ = 1.5406 Å). SEM images of samples
were performed on a FEI-Q FEG250 microscope, equipped with an EDAX
system. XPS data were recorded on an ESCALAB 250 spectrometer with
a monochromatized Al Kα1 X-rays as the excitation
source. All binding energies were corrected by fitting the C 1s peak
of surface adventitious carbon at 284.8 eV. The optical absorption
of the samples was studied using a Lambda-950 UV–vis spectrometer.
The steady-state PL spectra were recorded on an Edinburgh FLS980,
under an excitation wavelength of 380 nm. Nitrogen adsorption–desorption
isotherms at 77 K were carried out on a Micromeritics 3Flex surface
analyzer. Before the measurement, all the samples were degassed at
130 °C for 12 h under flowing N2. TEM images were
obtained on a CM200FEG PHILIPS operated at 200 kV, equipped with an
EDAX system and a GATAN Tridiem Image Filter. TGA was performed from
room temperature to 800 °C at a heating rate of 10 °C min–1 under O2. Fluorescence lifetime data were
acquired on a home-built confocal FLIM microscope based on a single
photon counting (TCSPC) device (Picoquant). The pulse frequency of
the 485 nm laser diode was set at 5 MHz, and the emission was filtered
by a 530 ± 25 nm bandpass filter.
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2

Scanning Electron Microscopy of Fungal Wheat Colonization

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To estimate the ability of the F. culmorum KF846 and T. atroviride AN240, T. viride AN430, and C. rosea AN291 strains to colonize wheat kernels, scanning electron microscopic (SEM) observations were performed. In the semi-field experiment, two ears collected from each positive control plot and each plot inoculated with a single fungus strain were used for the analysis. Plant material for SEM was prepared exactly as described by Basińska-Barczak et al. [39 (link)] by fixation in a mixture of 4% methanol-free formaldehyde and 0.5% glutaraldehyde (Polysciences, Hirschberg an der Bergstrasse, Germany) with the addition of phosphate buffered saline (PBS). SEM imaging was performed using a Quanta FEG 250 microscope (FEI) in low vacuum mode at 70 Pa pressure and 10 kV beam accelerating voltage with 30 µm aperture, with a working distance of 10 mm.
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