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Carbon film

Manufactured by Ted Pella
Sourced in United States

Carbon film is a thin layer of carbon material used as a support for microscopic samples in various scientific and analytical applications. It provides a stable and uniform surface for mounting and observing samples under high-magnification microscopes, such as transmission electron microscopes (TEM) and scanning electron microscopes (SEM).

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7 protocols using carbon film

1

Optical Properties of Ag2S and Li-doped Ag2S NPs

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The absorption spectra of the solutions containing 0.01 g of Ag2S and Li-doped Ag2S NPs (in 10 mL of chloroform) were measured using a SolidSpec-3700 UV–Vis–NIR spectrophotometer from Shimadzu. The photoluminescence (PL) spectra were measured by a Fluorolog-3 in TCSPC mode (HORIBA Scientific). All samples were excited by a CW 450 W xenon source, and directed to a single-grating spectrometer. The PL spectra were obtained using an InP/InGaAs detector equipped with an LN cooler. All TEM images were acquired on a JOEL JEM-2100F transmission electron microscope operating at 200 kV. The TEM samples were prepared by drop casting very thin nanoparticle solutions onto a 200 mesh copper grid with a carbon film (Ted Pella). Then X-ray diffraction spectroscopy (XRD) was conducted using a Rigaku D/MAX-220 V X-ray diffractometer coupled with a Cu K-alpha (1.540598 Å) source. The FT-IR was measured by EQUINOX 55 (Bruker). The Zeta potential and DLS were measured by ELS-77 (Otsukael).
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2

Characterization of Polypyrrole-Coated Carbon Nanofibers

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All of the dispersions of PPy@CNFs were diluted
to 0.01 wt % for the DLS and TEM analysis. The DLS measurement was
conducted by utilizing a helium–neon laser with a wavelength
of 632.8 nm and a scattering angle of 173°. The refractive index
(RI) and viscosity of the Milli-Q dispersant were specified to be
at 1.324 and 0.887 × 10–3 Pa s–1, correspondingly. The samples were characterized by RI and absorption
values of 1.595 and 0.200, respectively. For TEM, about 5 μL
of the sample was sedimented on a copper grid coated with carbon film
(200 mesh, Ted Pella Inc. USA) and then incubated at room temperature
for 3 min, and the excess liquid was drained with filter paper. The
processed samples were loaded onto a JEM-1400 PLUS TEM microscope
(JEOL Ltd., Japan) and evaluated in bright field mode with an accelerating
voltage of 80 kV. Only the LCNF sample was stained.
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3

Optical Properties of Ag2S and Li-doped Ag2S Nanoparticles

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The absorption spectra of solutions containing 0.01 g of Ag2S and Li-doped Ag2S NPs (in 10 mL of chloroform) were measured using a SolidSpec-3700 UV-Vis-NIR spectrophotometer from Shimadzu. The photoluminescence (PL) spectra were measured by a Fluorolog3 with TCSPC mode (HORIBA Scientific). All samples were excited by a CW 450 W xenon source, and directed to a single-grating spectrometer. The PL spectra were obtained using a InP/InGaAs detector equipped with an LN cooler. All TEM images were acquired on a JOEL JEM-2100F transmission electron microscope operating at 200 KV. The TEM samples were prepared by drop-casting very thin nanoparticle solutions onto a 200 mesh copper grid with a carbon film (Ted Pella). X-ray diffraction spectroscopy (XRD) for the NPs was performed using a Rigaku D/MAX-220 V X-ray diffractometer equipped with Cu K-alpha (1.540598 Å) source.
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4

Characterization of Quantum Dot Nanocrystals

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All TEM images were acquired on a JOEL 2010 Advanced High Performance TEM operating at 200 KV with a lanthanum hexaboride cathode. TEM samples were prepared by drop casting a purified solution of QDs from hexanes onto a 400 mesh copper grid with a carbon film (Ted Pella). ImageJ was employed to generate the volume-weighted size distributions shown in Fig. 2a. The images were Fourier transformed using the built-in ‘Bandpass Filter' option. The threshold was adjusted to match the QD dimension and the average 2D projection area of the NCs in the TEM was measured. TEM images of CSS QDs can be found in Supplementary Fig. 10. Assuming a spherical shape, the crystal volume was obtained via eq. (2):

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5

Peptide-Bacterial Component Interactions

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One part of the 10 mM peptide stock solution was added to 99 parts of the 1 mg/mL bacterial component (LPS, LTA, or PGN) solution to obtain a mixture with 0.1 mM peptides and 1 mg/mL bacterial components. Three μL of each mixture was dispersed onto a negatively charged copper grid with a carbon film (Ted Pella Inc., Redding, CA, USA). The specimen was first washed with a droplet of DI water twice and then stained with 5 μL of 0.75% uranyl formate for 45 s. After negatively stained, the TEM specimens were imaged using a Tecnai G2 F30 (FEI, Hillsboro, Oregon, USA) at an accelerating voltage of 300 kV.
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6

Low-Magnification TEM Imaging of Nanoparticles

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Lower magnification
(<300 k×) TEM imaging was performed on a FEI Tecnai T20 with
a LaB6 filament and Orius CCD, operated at 200 kV. Samples were prepared
on copper TEM grids with carbon films (Ted Pella) by drop-casting
a 2–5 μL drop of NP solution and drying in air for at
least 30 min.
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7

Transmission Electron Microscopy of CS/LBGS Nanoparticles

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The morphological examination of CS/LBGS nanoparticles was conducted by transmission electron microscopy (TEM; JEM-1011, JEOL, Japan). The samples were stained with 2% (w/v) phosphotungstic acid and placed on copper grids with carbon films (Ted Pella, USA) for TEM observation.
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