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Tecnai g2 f30 microscope

Manufactured by Thermo Fisher Scientific
Sourced in United States

The Tecnai G2 F30 is a transmission electron microscope (TEM) designed for high-resolution imaging and analysis of materials at the nanoscale. It features a field emission gun (FEG) electron source, advanced optics, and a range of specialized detectors to enable versatile imaging and analytical capabilities.

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13 protocols using tecnai g2 f30 microscope

1

Comprehensive Characterization of Nanomaterials

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X-ray diffraction (XRD) patterns were recorded on a X'Pert PRO X-ray diffractometer equipped with Cu Kα (λ = 1.54178 Å) radiation. Transmission electron microscopy (TEM) was carried out on a FEI Tecnai G2 F30 microscope. High-resolution TEM (HRTEM) was carried out on a FEI Tecnai G2 F30 microscope. Dynamic light scattering was measured using a particle size analyzer (ZetaPALS, Brookhaven Instruments). X-ray photoelectron spectroscopy (XPS) measurements were carried out on an Axis Ultra imaging photoelectron spectrometer (Kratos Analytical Ltd). Magnetization was measured by a superconducting quantum interference device (SQUID). The concentrations of Fe were quantified using an inductively coupled plasma-atomic emission spectrometer (ICP-AES, Profile, Leeman, USA). Fourier transform infrared radiation (FT-IR) spectrum was determined using a Nicolet 6700 spectrometer. Ultraviolet visible (UV-vis) absorption spectra were measured on a HACH DR6000 ultraviolet visible absorption spectrometer.
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2

Comprehensive Characterization of Pt-based Samples

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The crystal structure of the Pt-based samples was characterized by X-ray powder diffraction (XRD) using a Rigaku D/max-ga X-ray diffractometer with graphite monochromatized Cu Kα radiation (λ = 1.54178 Å). Transmission electron microscopy (TEM) images of such samples were taken using a HITACHI HT-7700 microscope operated at 100 kV. High-resolution transmission electron microscopy (HRTEM) was performed using a FEI Tecnai F30 G2 microscope operated at 300 kV. High-angle annular dark-field scanning TEM (HAADF-STEM) and Energy dispersive X-ray (EDX) mapping analyses were taken on a FEI Titan ChemiSTEM equipped with a probe-corrector and a Super-X EDX detector system and operated at 200 kV. The percentages of the elements in the samples were determined using inductively coupled plasma atomic emission spectrometry (ICP-AES, IRIS Intrepid II XSP, TJA Co., USA). Gas chromatography mass spectrometer (GC-MS) measurements were performed on a GC-MS 7890A-5975C (Agilent) with molecular ion selective monitoring. All of these samples were diluted with acetone in fixed ratio before the GC-MS measurement.
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3

Cryo-EM Analysis of ZIKV Virions

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ZIKV-316Q/461G virions were prepared for TEM analysis as described previously42 (link). Briefly, virus was precipitated from clarified culture supernatants using PEG 8000, resuspended in NTE buffer (10 mM Tris pH 8, 120 mM NaCl, 1 mM EDTA) before ultracentrifugation through a 20% sucrose cushion and a final purification step on a 10–40% potassium tartrate gradient. The virus band was harvested and buffer exchanged into NTE and final preparations (4 μl) were applied to a freshly glow-discharged 400-mesh holey carbon-coated copper grids (Proscitech). Grids were blotted for 7 s, in 100% relative humidity before plunge-freezing in liquid ethane using a Vitrobot (FEI). Cryo-EM images were acquired at 300 kV with an FEI Tecnai F30 G2 microscope, equipped with a K2 summit direct electron detector (Gatan).
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4

Comprehensive Materials Characterization

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The structure of
the samples was characterized by XRD patterns (D8 ADVAHCL instrument,
Bruker, Germany), FTIR spectroscopy (FTIR TENSOR 27 spectrophotometer,
Bruker, Germany), and Raman spectroscopy (Labram HR800 Raman system,
HORIBA, America). The morphologies of the samples were observed by
SEM (Sigma 300 microscope, ZEISS, Germany) and TEM (Tecnai F30G2 microscope,
FEI, Netherlands). The static water contact angles (SWCA) of the samples
were measured with a homemade apparatus. A 5 μL water droplet
was carefully dripped onto the samples, and the average SWCA value
was obtained by measuring 10 different positions on the sample.
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5

Structural Characterization of Nanoparticles

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Transmission electron microscopy (TEM) images of the obtained samples were taken using a HITACHI HT-7700 microscope operated at 100 kV. High-resolution transmission electron microscopy (HRTEM) was performed using a FEI Tecnai F30 G2 microscope operated at 300 kV. High-angle annular dark-field scanning TEM (HAADF-STEM) and Energy Dispersive X-ray (EDX) mapping analyses were taken on a FEI Titan ChemiSTEM equipped with a probe-corrector and a Super-X EDX detector system. This microscope was operated at 200 kV with a probe current of 50 pA and a convergent angle of 21.4 mrad for illumination. The X-ray diffraction (XRD) patterns were recorded on a Miniflex600 X-ray diffractometer in a scan range of 10–80° at a scan rate of 10° min−1. The percentages of Pd, Pt, and Cu in the samples were determined using inductively coupled plasma atomic emission spectrometry (ICP-AES, IRIS Intrepid II XSP, TJA Co., USA). TGA analysis was performed with a thermogravimetric analyzer (SDT Q600). The temperature was scanned from room temperature to 800 °C with a scan rate of 10 °C min−1.
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6

Comprehensive Characterization of Nanomaterials

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SEM and TEM images were recorded using an
EVO-18 microscope (ZEISS, Oberkochen, Germany) and an FEI Tecnai-G2
F30 microscope (FEI Co., Hillsboro, OR) spectrometer, respectively.
XPS spectra were obtained using a K-α spectrometer (Thermo Fisher
Scientific Co., Waltham, MA). The FTIR spectra were collected with
a Spectrum 65 FTIR spectrophotometer (PerkinElmer Co., Ltd., Waltham,
MA). The UV–vis absorption spectra were obtained using a Shimadzu
UV-6100 UV–vis-NIR spectrophotometer (Shanghai Mapada Instruments
Co., Ltd., Shanghai, China). Red excitation light was provided by
a PEAC 200A system (Ada Hengsheng Technology Development Co., Ltd.,
Tianjin, China). The distance between the illumination source and
the sample cell was maintained at 10 cm. PEC measurements were performed
using an electrochemical workstation (CHI760e, Chenhua Instrument
Co., Ltd., Shanghai, China). ITO slices (≤6 Ω, South
China Xiangcheng Technology Co., Ltd., Shenzhen, China) with an active
surface area of 0.25 cm2 were used as the working electrode
vs Ag/AgCl as the reference electrode.
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7

Synthesis and Characterization of Silica Nanoparticles

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Triton X-100 (9002-93-1), cyclohexane (110-82-7), 3-aminopropyltriethoxysilane (APTES, 919-30-2), ethyl silicate (tetraethyl orthosilicate; TEOS, 78-10-4), acetone (67-64-1), and AVAs (108605-69-2) were purchased from Darwin Reagent Co., Ltd., (Beijing, China). The ultrapure water was purchased from the A.S. Watson Group (Hong Kong, China). The SEM images were acquired using an SU 8020 microscope (Hitachi, Tokyo, Japan). The TEM images were recorded using a FEI Tecnai G2 F30 microscope (FEI; Hillsboro, OR, USA) at an accelerating voltage of 200 kV. The FT-IR was collected by a Vertex 70 spectrometer (Bruker, Bremen, Germany). The ultraviolet spectrophotometry was performed using a Cary 100 UV-Vis spectrometer (Agilent, Santa Clara, CA, USA). The fluorescence characteristics were recorded with a Biotek Synergy H1 Multi-Mode Microplate Reader (BioTek; Winooski, VT, USA).
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8

Characterization of Realgar Quantum Dots

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Ultravoilet-visible (UV-vis) absorption spectrum was recorded on a Shimadzu UV 2450PC spectrophotometer (Shimadzu Corp., Kyoto, Japan). Photoluminescence (PL) spectrum was monitored on a Perkin Elmer LS 55 luminescence spectrometer (PerkinElmer Inc., Waltham, MA, USA). High-resolution (HR) transmission electron microscopy (TEM) images were obtained with an FEI Tecnai G2F30 microscope (FEI, Hillsboro, OR, USA). The as-prepared realgar QDs were appropriately diluted with Milli-Q water before instrumental analysis.
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9

Characterization of Nanomaterial via SEM, HRTEM, XRD, and Raman

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Scanning electron microscope (SEM) images were obtained using a HITACHI S-4800 microscope (Japan). High-resolution transmission electron microscopy (HRTEM) images were obtained using a FEI Tecnai G2 F30 microscope (USA). The phase purity of the product was characterized by X-ray diffraction (XRD, German Bruker AXSD8 ADVANCE X-ray diffractometer) using an X-ray diffractometer with Cu KR radiation (λ = 1.5418 Å). The ultraviolet-visible (UV-Vis) diffuse reflectance spectra were obtained on an America Varian Cary 5000 spectrophotometer. Raman spectra were measured using a Britain Renishaw inVia Raman spectrometer at room temperature.
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10

Comprehensive Characterization of Rhenium-Doped Quantum Dots

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UV-vis absorption spectrum was recorded on a Shimadzu UV 2450PC spectrophotometer (Shimadzu Corp.). PL spectrum was monitored on a Perkin Elmer LS 55 luminescence spectrometer (PerkinElmer Inc.). Upconversion fluorescence spectrum was recorded by a Tsunami® femtosecond Ti:sapphire oscillator (Spectra-Physics, Santa Clara, CA, USA). HRTEM images were observed with a FEI Tecnai G2F30 microscope (FEI). The as-prepared RQDs were appropriately diluted with Milli-Q water before instrumental analysis. Scanning electron microscopy (SEM) images were taken by a Hitachi S-4300 microscope (Hitachi Ltd., Tokyo, Japan). To prepare the samples for SEM imaging, dried precipitates obtained by adding formic acid into the solution of synthesized RQDs were firstly scattered onto carbon conductor tape followed by coating with gold.
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