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Quanta 600 scanning electron microscope

Manufactured by Thermo Fisher Scientific

The Quanta 600 is a scanning electron microscope (SEM) manufactured by Thermo Fisher Scientific. The core function of the Quanta 600 is to produce high-resolution images of small-scale structures and surfaces by scanning them with a focused beam of electrons.

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4 protocols using quanta 600 scanning electron microscope

1

Comprehensive Characterization of Sb2(S1-xSex)3 Thin Films

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Raman analysis was performed on the hydrazine precursor solutions including Sb-S, Sb-Se, Sb-S-Se and S-Se solutions in a backscattering confocal configuration at room temperature. A LabRAM in Via Raman system was applied for measurement, and the unpolarized light was generated through a 532 nm Ar laser with power adjusted to 50 mW. Prior to measurement, each solution was sealed in a glass vial by parafilm in order to minimize oxygen and moisture exposure. X-ray diffraction (XRD) characterization (Philips, X pert pro MRD, with Cu Kα radiation, λ = 1.54178 Å) was performed on the annealed Sb2(S1-xSex)3 thin films prepared on TiO2 substrates. The compositions of the thin films were obtained through energy dispersive spectroscopy (FEI Quanta 600 scanning electron microscope, 20 kV). Sb2S3 powder (99.999%, Alfa Aesar) and Sb2Se3 powder (99.999%, Alfa Aesar) were used as standards for the calibration of EDS measurements. Scanning electron microscopy (FEI Nova NanoSEM450, without Pt coating) and UV-vis-NIR transmission spectroscopy (Perkin Elmer Instruments, Lambda 950 using integrating sphere) was performed on the Sb2(S1-xSex)3 films to determine the surface morphology and band gap, respectively.
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2

Multi-analytical Tool Wear Analysis

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Wear traces on archaeological and experimental tools were recorded following a multi-analytical and multi-scalar approach87 (link), which relies on the combination of optical, 3D digital, and scanning electron microscopy (Table S6). Archaeological tools were examined at the lithic laboratory of IPHES first using a 3D digital microscope Hirox KH-8700 for low-power observations (magnifications ranging from 35 × to 140 ×). Lateral lighting was used to record all the macro-scars visible on the edges to describe their initiation, termination, morphology, orientation, and distribution95 ,96 (link). High-power observations were conducted with a metallurgical microscope Zeiss Axio Scope A1 using incident lighting (magnifications 50 ×–500 ×), which enabled the observation of polish, edge rounding, striations, and micro-scarring. Use polish, edge rounding, and striations were described according to the principles outlined in several publications92 ,97 ,98 , and hafting traces were interpreted following guidelines stated by Rots33 ,84 . Finally, when necessary, a Fei Quanta 600 scanning electron microscope was used in low-vacuum mode (35 ×–2000 ×) to supplement and assist optical identification of wear traces, primarily polish and striations.
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3

Microstructural Evolution in Impacted UFG Al

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After the projectile penetration experiments, the shape of the perforated holes in UFG Al film was examined by using an FEI Quanta 600 scanning electron microscope operated at 10 kV. TEM analysis was performed on an FEI Tecnai F20 ST microscope operated at 200 kV to characterize the evolution of the microstructure near the impacted regions. To further probe the impact-induced microstructural changes in the UFG Al films, HRTEM experiments were performed.
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4

Microneedle-based Vaccine Delivery

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The microneedles were sputter-coated with gold using a Pelco SC-7 Auto Sputter Coating system. The samples were then imaged under an FEI Quanta 600 scanning electron microscope (SEM). To characterize the purity and activity of VLPs after loading into the microneedles, a microneedle extract was prepared by dissolving the patches in PBS and characterizing the released VLPs using the methods listed above. Polymer removal was done using Amicon ultracentrifugal filter units (EMD Millipore), as required for characterization.
To determine the penetration efficiency of the microneedles, pigskin was purchased from a local grocer and microneedles loaded with Qβ-Alexa were inserted into a spring applicator and held against the skin for 2 min after spring-assisted application. The top view and cross section of the skin were visualized under a fluorescence microscope (EVOS).
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