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Jem 2010 microscope

Manufactured by Bruker
Sourced in Japan

The JEM-2010 is a transmission electron microscope (TEM) designed and manufactured by Bruker. It is a high-performance instrument capable of providing detailed images and analytical data at the nanoscale level. The JEM-2010 is equipped with advanced optics and a robust design to enable high-resolution imaging and precise elemental analysis.

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2 protocols using jem 2010 microscope

1

Comprehensive Material Characterization

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Scanning electron microscope (SEM) images were obtained by a JSM-6480A microscope (Japan Electronics). Transmission electron microscope (TEM) images were taken on a JEM-2010 microscope (JEM-2010, Japan) with an accelerating voltage of 120 kV. The X-ray diffractograms (XRD) from a Bruker D8 Advance diffractometer (Bruker, USA). The samples were also analyzed with a Raman microscope with 512 nm laser excitation (Horba JobinYvon, France), FT-IR spectrometer (Bruker Vertex 70) and X-ray photoelectron spectroscopy (XPS) (Thermo Fisher Scientific, USA) operating with Al-Kα radiation. The N2 absorption-desorption isotherms of the samples were tested with liquid nitrogen (78 K) adsorption by the Brunauer-Emmet-Teller method (Autosorb iQ Station 2, Quantachrome Instruments, U.S.A.). The thermogravimetry analyses were performed on a simultaneous thermal analyzer (Netzsch STA 449F3, Germany).
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2

Multimodal Characterization of Nanocluster Alloys

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The alloying reaction was conducted in an Eppendorf Comfort thermomixer. UV–vis absorption spectra of the samples were obtained from a Shimadzu UV-1800 spectrometer. Cluster concentrations were measured by ICP-OES on a Thermo Scientific iCAP 6000. Scanning transmission electron microscopy and energy dispersive X-ray spectroscopy elemental mappings were recorded on a JEOL JEM 2010 microscope operating at 200 kV. ESI-MS analysis was carried out on a Bruker microTOF-Q system in negative ion mode. Detailed operating conditions of ESI-MS analysis are given as followings: source temperature/120 °C, dry gas flow rate/4 L per min, nebulizer pressure/0.4 bar, and capillary voltage/3.5 kV. In a typical ESI-MS analysis, 0.2 mL of DMF solution of NCs (with a NC concentration of ~0.64 mM) was injected with a flow rate of 3 μL per min. PAGE was carried out on a Bio-Rad Mini-Protean Tetra Cell system, with a stacking and resolving gel prepared from 4 and 30 wt.% acrylamide monomers, respectively. In a typical analytical gel (1.0 × 83 × 73 mm, 10 wells), 10 μL of aqueous NC solution containing 5 vol.% glycerol was loaded into each well, followed by running the gels at a fixed voltage of 200 V at 4 °C for 4 h.
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