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Jem 2010 uhr

Manufactured by JEOL

The JEM-2010 UHR is a high-resolution transmission electron microscope (HRTEM) manufactured by JEOL. It is designed to provide high-resolution imaging and analysis capabilities for a wide range of materials and applications. The JEM-2010 UHR features a 200 kV electron beam, advanced optics, and a range of analytical capabilities to support in-depth characterization of samples at the nanoscale.

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4 protocols using jem 2010 uhr

1

Uranium Nanoparticle Characterization by TEM

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To observe uranium-bearing loci by TEM, we fabricated electron-transparent ultrathin sections with a focused ion beam (FIB) sample preparation technique using a Hitachi FB-2100 instrument (Ibaraki, Japan) with a micro-sampling system. Before FIB fabrication, the thin section sample was coated by a carbon film and inserted into the FIB apparatus, then locally coated with the deposition of W (100–500 nm thick) for protection, trimmed using a Ga ion beam at an accelerating voltage of 30 kV and thinned down to a final thickness of 100–200 nm with a low energy beam of 10 kV as a final process. FIB-fabricated ultrathin sections were placed on a Cu specimen support with W deposition and observed by TEM. TEM examinations were performed at an accelerating voltage of 200 kV using a JEOL JEM-2010 UHR (LaB6 electron gun) with a nominal point resolution of ~0.2 nm. TEM-EDS was used for elemental analysis of U-bearing nanoparticles and Mg- and Fe-bearing aluminosilicate.
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2

Characterization of GO/PDA/Cu NPs Composite

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The microstructure and composition of GO/PDA and GO/PDA/Cu NPs were characterized by TEM (JEM-2010 UHR, JEOL) and XPS (ESCALAB 250, Thermo Fisher Scientific) using the Al Kα radiation (1486.6 eV, 15 kV, 150 W) at a vacuum of 2×10−9 mbar. Electrochemical measurement was performed at room temperature in phosphate buffer (PBS) on the CHI 660e potentiostat (CH Instruments Inc., Shanghai, China). A simple three-electrode configuration used in the measurement consisted of an Ag/AgCl electrode as the reference electrode, a Pt wire as the counter electrode, and a glassy carbon electrode (GCE, 3 mm in diameter) modified with GO/PDA/Cu NPs composite as the working electrode.
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3

Characterization of Zinc Oxide Nanorods

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The electrodes morphologies were examined by field emission scanning electron microscopy (FESEM, Hitachi S4700, and SUPRA 40VP) equipped with an energy dispersive X-ray (EDX), and high-resolution transmission electron microscopy (HRTEM, JEOL JEM-2010UHR) with selected area electron diffraction (SAED) at an acceleration voltage of 200 kV. The crystalline structure of as-synthesized ZNRs was analyzed using X-ray diffractometer (XRD, Rigaku) with Cu-Kα radiation (λ = 1.54178 Ǻ) in the range of 10–90° with 8°/min scanning speed. In addition, the optical properties of ZNRs were characterized by Raman-scattering measurements with Ar+ (513.4 nm) as the exciton source.
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4

Microparticle Analysis by Advanced TEM

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Cross-sectional thin TEM specimens were prepared from radioactive microparticles using a focused ion beam (FIB) instrument with micro-sampling system (Hitachi FB-2100) as described in the supplementary information. Then specimens were initially examined using a TEM (JEOL JEM-2010UHR) operated at 200 kV with an EDS analyzer system (JEOL JED-2200). Elemental mapping in the microparticles and quantitative analyses were performed using a JEOL JEM-3100FEF operated at 300 kV in the STEM mode, with an EDS analyzer system (Thermo Fisher Scientific NORAN System SIX). Finally, elemental maps for nanoparticulates inside the microparticles were acquired using a JEOL JEM-2800 operated at 200 kV with double wide-area (0.95 sr.) silicon drift detectors (SDD) for EDS analyses.
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