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Tecnai g2 f30 s twin tem

Manufactured by Thermo Fisher Scientific
Sourced in Japan, United States

The Tecnai G2 F30 S-Twin TEM 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) source, a twin-objective lens system, and advanced image processing capabilities. The core function of this instrument is to provide researchers with the ability to study the structure, composition, and properties of materials at the atomic and molecular level.

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9 protocols using tecnai g2 f30 s twin tem

1

Characterization of Catalysts by Spectroscopy

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Powder
X-ray diffraction (XRD) was performed on an Empyrean diffractometer
(Malvern Panalytical, Shanghai, China) with Cu Kα radiation
(k = 1.54056 Å); scanning electron microscopy
(SEM) images were obtained on an S-4800 SEM (Hitachi, Japan); and
transmission electron microscopy (TEM) images were obtained on a Tecnai
G2 F30 S-Twin TEM (FEI Company). Elemental analysis of catalysts and
the concentrations of leached metal ions during the Fenton reaction
were determined by inductively coupled plasma (ICP)-optical emission
spectroscopy (OES) on an Optima 2000 ICP-OES (PerkinElmer Instruments).
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2

Comprehensive Characterization of Catalysts

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The crystalline phases in the samples were investigated by powder XRD with a Rigaku D/max2500 diffractometer (CuKα1 radiation, λ = 1.54059 Å). The metal loadings were tested by ICP-MS on a VISTA MPX (Varian, Inc.). The porous structure was analysed with N2 adsorption–desorption experiments conducted at 77 K on a Quantachrome SI-MP Instrument. The morphology was characterized by field-emission SEM on a JSM-7800F operating at 15 kV and TEM on a JEOL-2100F. The HRTEM images and element mappings were collected using Tecnai G2 F30 S-Twin TEM (FEI, The Netherlands) operated at 200 kV. The HAADF-STEM images were obtained by using a JEOL JEM-ARM200F S/TEM with a spherical aberration corrector. The XAFS analysis of Fe K-edge, Co K-edge, Ru K-edge, Ir K-edge, and Pt L3-edge, and their corresponding references were obtained at the 1W1B station of the Beijing Synchrotron Radiation Facility that was operated at 2.5 GeV with a maximum current of 250 mA. The acquired EXAFS data were analysed according to the standard procedures using the ATHENA module implemented in the IFEFFIT software packages (see the details in Supplementary Materials)
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3

Comprehensive Characterization of Photocatalytic Materials

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TEM (JEOL, JEM-2100) and HRTEM (FEI, Tecnai G2 F30 S-Twin TEM) were measured for imaging. The phase composition was measured by the Bruker D8 ADVANCE X-ray diffractometer (XRD). BET-specific surface areas and pore structures were determined by a Beishide 3H-2000PS2 system. XPS measurement was performed on a Thermo Scientific ESCALAB 250Xi spectrometer. The photocurrent response experiment was performed on a photoelectrochemical workstation (CIMPS-2, Zahner) with a three-electrode system; 300 W Xe lamp and Na2SO4 aqueous solution (0.1 M) were used as the light source and electrolyte solution, respectively. The hydroxyl radicals were detected using a fluorescence spectrophotometer (Hitachi F-7000).
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4

Comprehensive Characterization of Catalysts

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An X-ray diffraction (XRD) analysis of the catalysts was carried out at the XPert Pro MPD (PANalytical B.V., Almelo, The Netherlands) with Cu-Kα radiation generated at 45 kV and 40 mA. The morphologies of the catalysts were charactered by means of field emission scanning electron microscopy (FESEM, S-4800; Hitachi, Tokyo, Japan), which was operated at an accelerating voltage of 4 kV. The transmission electron microscopy (TEM) investigation was performed at the Tecnai G2F30 S-Twin TEM (FEI, Amsterdam, The Netherlands). The X-ray photoelectron spectroscopy (XPS) experiments were performed with a Thermo Scientific ESCA-Lab-200i-XL spectrometer (Waltham, MA, USA), which utilized monochromatic Al Alα radiation (1486.6 eV), and the C 1s and N 1s peak spectra were analyzed by using XPS Peak 4.1 software. To quantify the specific surface areas of examined catalysts, Brunauer–Emmett–Teller analysis was performed (BET, ASAT 2020M+C, Micromeritics, Micromeritics Instrument Co., Norcross, GA, USA), using the nitrogen adsorption and desorption isotherms at liquid nitrogen temperature (77 K). UV-Vis diffuse reflectance spectroscopy was recorded on a UV/Vis spectrophotometer (UV/Vis DRS, UV-2550, Shimadzu, Tokyo, Japan) over the wavelength range between 200 and 800 nm.
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5

Nanomaterial Characterization Techniques

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The morphology of the as-prepared nanostructures was studied with a S-4800 II field-emission scanning electron microscope (SEM) and a Tecnai 12 transmission electron microscope (TEM) (Philips). The high-resolution transmission electron microscope (HRTEM) image and selected area electron diffraction (SAED) image were captured by using a Tecnai G2 F30 S-Twin TEM (FEI). The chemical composition of the AuNPs–AgNWs was also analyzed by using a S-4800 II field-emission scanning electron microscope. The optical density (OD) at 450 nm of CCK-8 was measured by using a Cary UV-5000 spectrometer.
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6

Characterization of Au-AgNSs and MBs

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The UV–visible absorption spectra were obtained from a UNICO 2100 PC UV–Vis spectrophotometer (Japan). All Raman spectra were recorded with a Renishaw InVia Raman Microscope Spectrometer (UK) with excitation at 785 nm and 50 × objective lens. The WiRETM software of Renishaw was used for Raman system operation and data acquisition. To repress the background noises of instrument, smoothing and baseline correction were applied. Tecnai 12 transmission electron microscope (Philips) was used to achieve the transmission electron microscopy (TEM) images of Au-AgNSs and MBs, operating at an accelerating voltage of 60 kV. S-4800 II field-emission scanning electron microscope (Hitachi) was applied for the scanning electron microscopy (SEM) images of Au-AgNSs and MBs, operating at 1.0 kV. The selected area electron diffraction (SAED) images and high-resolution TEM (HRTEM) were obtained with a Tecnai G2 F30 S-Twin TEM (FEI) at 200 kV.
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7

Structural Characterization of Perovskite Powders

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XRD patterns of the perovskite powders were analyzed by using filtered Cu-Kα radiation (λ = 1.5418 Å) on an X-ray diffractometer (Rigaku Smartlab). Detailed structural information was extracted from the XRD refinements. SAED patterns were collected at 200 kV on a TEM instrument (JEM-2100 UHR, JEOL, Japan). HAADF-STEM image and corresponding elemental mapping were taken at 300 kV on a Tecnai G2 F30 S-Twin TEM (FEI, America). SEM image was performed on a Hitachi S-4800 scanning electron micro-analyzer. BET method (Quantachrome Autosorb-iQ3) was applied to obtain the specific surface areas of perovskite powders. Soft XAS spectra at O-K edge in TEY and FY modes were conducted at the TLS BL20A of the NSRRC in Taiwan. To calibrate the photon energy, a NiO sample was measured simultaneously for O-K edge.
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8

Characterization of Gadolinium-Doped Carbon Dots

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Nuclear magnetic resonance (NMR) spectra were recorded in D2O on Agilent Technologies 800/54 premium. Fourier transform infrared spectroscopy (FT-IR) was performed on Thermo Scientific Nicolet iS10 spectrometer. UV–vis absorption spectra were collected on Agilent Cary 60 spectrophotometer and Shimadzu UV-1900 spectrophotometer. The fluorescence spectra were measured on Hitachi F-7000. The fluorescence lifetime and quantum yield were recorded on an Edinburgh Instruments FLS980. Gadolinium in Gd@CDs was quantified by Thermo Fisher iCAP Qnova Series inductively coupled plasma mass spectrometry (ICP-MS). X-ray photoelectron spectroscopy (XPS) analysis was recorded by Kratos Axis Utra Dld. Raman spectra were measured on Labram Aramis with an excitation wavelength of 532 nm. The morphologies were observed with FEI Tecnai G2 F30 S-TWIN TEM. The hydrodynamic diameter and zeta potential of nanoparticles were measured by a PSS-Nicomp 380ZLS.
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9

Characterization of Nanomaterials via Spectroscopy

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The UV-visible absorption spectra were recorded with an Agilent Cary UV-5000 UV-vis spectrophotometer (USA). Transmission electron microscopy (TEM) images were characterized by Tecnai 12 TEM (Philips, Netherlands). Scanning electron microscopy (SEM) images were obtained with an S-4800II field emission SEM (Hitachi, Japan). High-resolution TEM (HRTEM) images, high-angle annular dark-field scanning TEM (HAADF-STEM) images, and selected area electron diffraction (SAED) were captured by Tecnai G2 F30 s-twin TEM (FEI, USA). Raman spectra of test lines were obtained on an inVia micro-Raman spectrometer (Renishaw, UK).
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