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Fei verios 460

Manufactured by Thermo Fisher Scientific
Sourced in United States

The FEI Verios 460 is a high-resolution field emission scanning electron microscope (FE-SEM) designed for advanced materials characterization. It features a high-brightness electron source and a range of imaging and analytical capabilities.

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7 protocols using fei verios 460

1

Scanning Electron Microscopy of Dried Samples

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The SEM analysis was conducted according to the method described by Tanpichai et al. [25 (link)] with minor modifications. Briefly, raw materials and papery food dried through vacuum freeze drying were glued on the sample holder using conductive adhesive and then coated with a thin gold layer using an ion sputtering instrument (JYSC-100, Guangzhou Jingying Scientific Instrument Co., Ltd., Guangzhou, China). Microscopic images of the samples’ surface were observed under a high-resolution field emission scanning electron microscope (FEI Verios 460, FEI company, Hillsboro, USA, OSU) at a magnification of 5000× and an acceleration voltage of 5 kV [26 (link)].
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2

Characterization of Graphene Oxide Powders

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Two electron microscopy studies were undertaken. The first study was a bright field transmission electron microscopy (TEM) investigation of the size, shape and topography of the various GO and RGO powder samples. The study was carried out using a Tecnai G2, FEI, (Electron Optics, USA) microscope operating at 100 kV. The second study used a high resolution field emission scanning electron microscope (FESEM: FEI-Verios 460) operating at 5 kV, with 0.10 nA current and operating under secondary electron mode. The FESEM was also used to examine the physical structure and topography of the GO and RGO powder samples. Prior to analysis, dried powder samples were deposited on carbon tape covered SEM holders and then sputter coated (E5000, Polaron Equipment Ltd.) with a 2 nm layer of platinum to prevent charge build up.
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3

SEM Imaging of Gold-Coated Samples

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Scanning
electron microscopy
(SEM) experiments were performed on an FEI Verios 460 instrument (Thermo
Fisher Scientific, Eindhoven, The Netherlands) equipped with an Everhart-Thornley
detector (EDT) using a 2 kV electron beam. The samples were sputter-coated
with a 20 nm gold layer.
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4

Characterization of AuNPs and AuNP-immersed Paper

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The morphology of the AuNPs and AuNP-immersed paper were characterized using a scanning electron microscope (SEM; FEI Verios 460, Thermo Fisher, Hillsboro, CA, USA) and a transmission electron microscope (TEM; FEI Talos F200S, Thermo Fisher, Hillsboro, CA, USA). The UV–VIS absorption spectrum of the synthesized AuNPs were obtained using a UV–VIS spectrophotometer (UV-5500PC, Shanghai Yuanxi Instrument Ltd., Shanghai, China). The results of the pesticides within the apple tissues were acquired by high performance liquid chromatography (HPLC; Agilent 1290B, Santa Clara, CA, USA).
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5

SEM Imaging of Monolith Cross-Sections

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SEM images of cross sections of the
monoliths were recorded on a FEI Verios 460 instrument (Thermo Fisher
Scientific, Eindhoven, The Netherlands) equipped with an Everhart–Thornley
detector (EDT) using a 2 kV electron beam. The samples were sputter-coated
with a 15 nm gold layer on top of a 5 nm layer of palladium.
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6

Morphological Characterization of PEDOT Films

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The morphology of the films and nanostructures was analyzed using field emission-scanning electron microscopy (FE-SEM, FEI VERIOS 460, Thermo Fisher Scientific, Waltham, MA, USA) with a 2 kV accelerating voltage. The thickness of the films was measured using a stylus profiler system (Vecco® Dektak, Bruker, Billerica, MA, USA). Raman spectroscopy was performed to analyze the vibrational modes of PEDOT films prepared to vary the deposition conditions: applied potential and electropolymerization time. These measurements were performed using a high-resolution Raman spectrometer (Horiba Jobin Yvon, Kioto, Japan) with a 532 m Nd:YAG laser (8.5 mW) from 200 to 1700 cm−1 in air at RT.
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7

Characterization of Fabricated Monoliths

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The modification of the PP housing and the polymerization were carried out using a Julabo water bath (900F, Julabo, Seelbach, Germany). The chromatographic separations were performed on an Agilent Technologies 1100 series system (Agilent, Waldbronn, Germany). For solvent delivery, a capillary pump (G1376A) was used. Other system components included an autosampler (G1313A) and a diode-array detector (G7117B). The morphological and topographical characterization of fabricated monoliths, was performed by scanning electron microscopy (FEI Verios 460, Thermo Fisher Scientific, Eindhoven, The Netherlands) with an Everhart-Thornley detector (EDT). The samples were sputter-coated with gold using an EM ACE600 Double sputter coater (Leica Microsystems, Amsterdam, The Netherlands).
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