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8 protocols using talos f200s transmission electron microscope

1

Comprehensive Characterization of Materials

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The powder X-ray diffraction (XRD) patterns were performed on a Panaco X′ Pert PRO X-ray diffractometer with Cu Kα radiation (l = 0.15406 nm) with the operation voltage and current maintained at 45 kV and 40 mA. Scanning speed: 1° min−1, test range: 10° ≤ 2θ ≤ 70°. Fourier transform infrared spectroscopy (FT-IR) analysis was carried out on a PerkinElmer FT-IR spectrometer. The scanning electron microscope (SEM) images were determined by Zeiss MERLIN Compact SEM-EDX microanalysis. TEM images and elemental mapping analysis of the samples were obtained on a FEI Talos F200S transmission electron microscope operating at 200 kV. The chemical states of different elements were determined by Thermo ESCALAB 250XI X-ray photoelectron spectroscopy (XPS). The UV-vis absorption spectra of the samples were measured on Shimadzu UV-1780 UV-vis-NIR spectrophotometer. The absorbance of the solution during the reaction was monitored by a 722N visible spectrophotometer.
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2

Advanced Material Characterization Techniques

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The morphology of the samples was observed by a scanning electron microscope with an operating voltage of 10 kV (SEM, Apreo S LoV ac, Thermo Fisher Scientific, Waltham, MA, USA).
The X-ray diffraction data were taken using an X-ray diffractometer with CuK radiation and a measurement range of 20–80°, (XRD, Miniflex 600, Akishima, Rigaku, Tokyo, Japan).
The transmission electron microscopy and selected area electron diffraction images were obtained from an FEI Talos F200s transmission electron microscope, operated at 200 kV (TEM, SAED, Thermo Fisher Scientific, Waltham, MA, USA).
High-resolution transmission electron microscopy was carried out on an FEI Titan Themis Z G3 30–300 spherical aberration-corrected transmission electron microscope, operated at 300 kV, equipped with both image and probe aberration (HRTEM, Thermo Fisher Scientific, Waltham, MA, USA).
X-ray photoelectron spectroscopy was used to characterize the atomic composition and state at the surface of the samples, using Al Ka rays as the excitation source (XPS, Thermo Scientific K-Alpha, Waltham, MA, USA).
The UV-Vis absorbance spectra were collected by a Cary 5000 spectrophotometer, (UV-Vis, Agilent, Santa Clara, CA, USA).
The photoluminescence spectra were acquired using a fluorescence spectroscopy test system (PL, FLS980, Edinburgh Instruments Ltd., Livingston, UK).
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Comprehensive Characterization of Optoelectronic Materials

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Photoluminescence (PL) and stability tests were acquired on an Ideaoptics FX2000-EX PL-spectrometer. Transmission electron spectroscopy (TEM) and high-angle annular dark-field scanning transmission electron microscope (HAADF-STEM) micrographs was performed on a FEI TalosF200s transmission electron microscope operating at 100 kV. Scanning electron microscopy (SEM) experiments were performed on FEI Nova NanoSEM 450. Fourier transform infrared spectroscopy (FTIR) measurements were carried out on a Thermo-Nicolet iS50 FTIR-spectrometer. The quantum efficiency (QE) measurements were carried out on an Ocean Optics QEpro QY test system under 390 nm blue laser irradiation. The infrared thermal images were recorded on an Optris PI200. The luminous efficiency and optical power were recorded on an EVERFINE ATA-1000 LED automatic temperature control photoelectric analysis and measurement system. Ultraviolet visible (UV-Vis) absorption spectra were tested on a Persee T6 UV-Vis spectrometer. Thermal gravimetric (TG) analysis was performed on a Beijing lasting Scientific Instrument Factory HCT-3 Microcomputer Differential Thermal Balance. The luminous efficiency and optical power were recorded on an EVERFINE ATA-1000 LED automatic temperature control photoelectric analysis and measurement system. The fluorescent thermal quenching was tested on an EVERFINE EX-1000 test system.
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4

Characterization of CuO Nanostructures

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The electrochemistry tests were conducted at a CHI 760E workstation (ChenHua, China). A Talos F200S transmission electron microscope (FEI, USA) and a Merlin Compact scanning electron microscope (Zeiss, Germany) provided the morphology results. Samples for transmission electron microscopy (TEM) were prepared by placing a drop of precipitate (dispersed in water by ultrasonication for 10 min) on a carbon-coated copper grid and allowing it to dry in air. The X-ray diffraction (XRD) measurements were implemented with a D8 Advance diffractometer (Bruker, Germany). The Raman spectra of the CuO nanostructures were recorded on a LabRAM HR Evolution spectrophotometer equipped with an Ar ion 514 nm laser (Horiba, Japan). The X-ray photoelectron spectra (XPS) were recorded on a K-Alpha spectrometer (Thermo, USA). The absorption spectral study was performed using a 1800PC UV-Vis spectroscope (Mapada, China) with a deuterium lamp as the irradiation source and phosphate-buffered saline (PBS) as the reference. A ZEN3690 Zetasizer (Malvern, UK) was applied to measure the zeta potential and size distribution, and the test temperature was 25 °C, the number of cycles was 10, and the dispersant was water.
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5

Comprehensive Material Characterization for Photocatalysis

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Powder X-ray diffraction (XRD) was tested on a Shimadzu Maxima X-ray diffractometer (XRD 7000) with Cu Kα radiation at a current of 30 mA and a voltage of 40 kV. The textural structures and surface morphologies of obtained samples were analyzed by a Scanning Electron microscope (SEM, HITACHI S-4800) and TEM images were performed on a FEI Talos F200S Transmission Electron microscope. X-ray photoelectron spectroscopy (XPS) was carried out using a ThermoFisher electron spectrometer (ESCSLAB 250Xi) with a monochromatized microfocused Al X-ray source. The binding energy was calibrated using C1s peak at 284.6 eV as the reference energy. Fourier Transform Infrared Spectroscopy (FTIR) was tested on a Shimadzu IRAffinity-1 using K-Br plate applied for observation of further structural information in the range of 4000 ~ 500 cm−1. The specific surface area, pore volume and pore size distribution of prepared photocatalysts were measured using a Quantachrome instrument and calculated by the nitrogen adsorption–desorption isotherms using the Brunauer–Emmett–Teller (BET) and Barrett-Joyner-Halenda (BJH) methods at liquid nitrogen temperature. The evolution amount of H2 was detected on a Shimadzu gas chromatograph (GC-2014C) by manual injection.
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6

Comprehensive Material Characterization Protocol

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The powder X-ray diffraction (XRD) pattern was measured on a Panaco X′ Pert PRO X-ray diffractometer with Cu Ka radiation (l = 0.15406 nm, the operation voltage: 45 kV, the operation current: 40 mA, scanning speed: 1° min−1, test range: 10° ≤ 2θ ≤ 70°). The transmission electron microscope (TEM) images were obtained on a FEI Talos F200S transmission electron microscope (the operation voltage: 200 kV). The Fine spectra of Fe and Pt were determined by Thermo ESCALAB 250XI X-ray photoelectron spectroscopy (XPS). The magnetometer hysteresis loops was measured on LakeShore 7404. The UV-vis absorption spectra were measured on Shimadzu UV-1780 UV-vis-NIR spectrophotometer. The absorbance at λ = 400 nm was monitored by a 722N visible spectrophotometer.
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7

Purification and Visualization of Baculoviruses

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The supernatant of Sf9 cells infected with recombinant baculovirus (multiplicity of infection (MOI) = 1) was collected at 4 dpi, and baculoviruses in the supernatant were purified by two rounds of sucrose gradient ultracentrifugation according to standard methods. The purified baculoviruses were adsorbed onto glow discharge-activated carbon-coated grids for 2 min. The sample-coated grids were washed three times with distilled water, following by negative staining with 1% uranyl acetate for 45 s. Images were acquired using an Talos F200S transmission electron microscope (FEI, Hillsboro, OR, USA).
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8

Structural Characterization of Fe(OH)3/Fe2O3@Au Nanocomposites

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The crystal structure and phase purity of the samples were measured by a Panaco X'Pert PRO X-ray diffractometer. A Panalytical Empyrean powder X-ray Cu-Kα radiation diffractometer with wavelength set to 0.15406 nm, commonly used voltage at 45 kV, current at 40 mA, and scanning speed: 2° min−1, was used for measurement in the following test range: 10° ≤ 2θ ≤ 70°. The elemental composition of the Fe(OH)3/Fe2O3@Au nanocomposites was determined by Zeiss MERLIN Compact SEM-EDX microanalysis. The chemical states of different elements were determined by Thermo ESCALAB 250XI X-ray photoelectron spectroscopy (XPS). TEM images of the samples were obtained on a FEI Talos F200S transmission electron microscope (acceleration voltage: 200 kV). The UV-Vis absorption spectra of the samples were measured on a Shimadzu UV-1780 UV-vis-NIR spectrophotometer. The absorbance of the solution during the reaction was monitored by a 722N visible spectrophotometer.
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