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Jem f200

Manufactured by Bruker
Sourced in Japan

The JEM-F200 is a field emission scanning electron microscope (FE-SEM) designed for high-resolution imaging and analysis of small samples. It provides a focused electron beam that scans the sample surface, allowing for detailed visualization and characterization of micro- and nano-scale structures.

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2 protocols using jem f200

1

Comprehensive Material Characterization

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The morphology,
elemental composition, and distribution of the samples were directly
characterized with SEM (JEOL JSM-7900F), TEM (JEOL JEM-F200), and
EDS (Bruker EDS QUANTAX). The lattice structures of composite were
registered using an X’Pert PRC diffractometer (Netherlands,
PANalytical) with Cu Kα radiation at a scanning rate of 5°
min–1 (λ = 0.15418 nm). The distribution and
valence state situation of various elements on the film surface were
analyzed via X-ray photoelectron spectroscopy (XPS, ThermoFisher ESCALAB
XI+). Electron paramagnetic resonance (EPR) measurement was carried
out on a Bruker ELEXSYS-II E500 spectrometer. The Raman spectra of
the samples were tested by a HJY LabRAM Aramis spectrometer with a
laser diode at an excitation wavelength of 532 nm.
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2

Synthesis and Characterization of SPIONs

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The SPIONs were synthesized using a thermal decomposition method presented in a previous study [49 (link)]. Briefly, 1.08 g iron(III) chloride and 3.65 g sodium oleate were dissolved in a 28 mL mixture of ethyl alcohol, distilled water (DW), and hexane. The mixture was thermally evaporated at 60 C for 4 hrs using a 3-neck flask under constant nitrogen influx to form an iron oleate complex. The mixture was washed with DW three times, and excess remaining hexane was evaporated at 40 C for 30 min using a rotary evaporator (SB-1300, Singapore). The collected 1.8 g iron oleate, 0.312 g oleic acid, and 3 g N-tetracosane were dissolved in 9 mL 1-octadecene. The mixture was evaporated at 320 C for 1 hr in a 3 neck flask with vigorous stirring to induce the nucleation/growth phase of nanocrystals. The resulting solution was cooled at room temperature, followed by the addition of 15 mL hexane. Synthesized SPIONs were separated from hexane using a magnetic field, and the SPION-containing solution was washed three times with acetone. The images and X-ray diffraction (XRD) pattern of SPIONs nanocrystals were obtained using transmission electron microscopy (TEM, JEM-F200, Japan) and XRD machine (D8 Advance, Bruker, USA) to characterize the crystals, respectively.
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