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Jsm 7500fam

Manufactured by JEOL
Sourced in Japan

The JSM-7500FAM is a field emission scanning electron microscope (FESEM) designed for high-resolution imaging and analysis of a wide range of samples. It features a high-brightness electron gun, advanced optics, and a high-sensitivity secondary electron detector to provide detailed surface information at the nanoscale level.

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9 protocols using jsm 7500fam

1

SEM/EDX Analysis of Samples

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The SEM/EDX analysis was carried out with a JSM-7500FAM (JEOL) at 5.0 kV. The working distance was about 3 × 4 mm. Samples were placed in dried oven maintained at 27 °C for 30 min and were sputter-coated with gold before SEM imaging.
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2

SEM Imaging of Coated Samples

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The SEM analysis was carried out with a JEOL JSM-5800 or JSM-7500FAM with 5.0 kV. The working distance was about 3 × 4 mm. Samples placed in dried oven maintained at 27 °C for 30 min and were sputter-coated with gold before SEM imaging.
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3

Morphological and Elemental Analysis of BG-Coated Ti

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Surface and cross-sectional morphologies of the abraded and alumina blasted Ti before and after BG coating were observed by field emission scanning electron microscope (FE-SEM, JSM-7500FAM, JEOL, Tokyo, Japan); also, the surface and cross-section elemental analysis of the BG coated Ti before and after blasting were evaluated using an energy-dispersive X-ray spectroscope (EDS, JSM-7500, JEOL). Phase structure of the BG 58S and abraded and blasted Ti before and after BG coating was analyzed by X-ray diffractometer (XRD) (Miniflex600, Rigaku, Tokyo, Japan). The diffractometer operated at 40 kV and 15 mA, with a 2θ range of 20°-80°, by utilizing a step size of 0.02.
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4

SEM/EDX Characterization of Samples

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The SEM/EDX analysis was carried out with a JSM-7500FAM (JEOL, Tokyo, Japan) at 5.0 kV. The working distance was about 3 × 4 mm. Samples were placed in a drying oven maintained at 27 °C for 30 min and were sputter-coated with gold before SEM imaging.
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5

SEM-EDX Sample Preparation Protocol

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The SEM / EDX analysis was carried out with a JSM-7500FAM (JEOL) with 5.0 kV. The working distance was about 3 × 4 mm. Samples were placed in dried oven maintained at 27 °C for 30 min and were sputter-coated with gold before SEM imaging.
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6

SEM/EDX Analysis of Gold-Coated Samples

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The SEM/EDX analysis was carried out with a JSM-7500FAM (JEOL, Tokyo, Japan) at 5.0 kV. The working distance was about 3 × 4 mm. Samples were placed in a drying oven, maintained at 27 °C for 30 min and were sputter-coated with gold before SEM imaging.
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7

Structure and Morphology Characterization of SnO2 Samples

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Powder X-ray diffraction (XRD) patterns of samples were obtained on a Rigaku RINT-2200 diffractometer using CuKα radiation. The SnO2 content in samples was estimated by thermogravimetric analysis (TGA, SEIKO Instrument Inc, TG/DTA7300). The specific surface areas were determined by αs-plot analysis23 (link),24 (link) from the N2 adsorption isotherm at 77 K (MicrotracBEL Co. Ltd. BELSORP-max). Pore size distribution and pore volume of samples were analyzed by Grand Canonical Monte Carlo (GCMC) method25 (link). The morphology of samples was observed by scanning electron microscope (SEM, JEOL JSM-7500FAM) and high-resolution scanning transmission electron microscope (HR-STEM; ARM-200CF, JEOL Ltd.). The SEM image and EDX analysis data of a cross-section of solid electrolyte/anode were taken on the material peeled off from the current collector sheet in an Ar-filled glove box after a half-cell construction described below.
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8

SEM and XRD Analysis of Coated Surface

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The morphology and fractured area of the treated surface was observed by SEM (JCM-6000 Plus, JEOL, Tokyo, Japan) and field emission scanning electron microscopy (FE-SEM: JSM-7500 FAM, JEOL) at 15 kV of accelerating voltage after the gold coating.
Phase identification X-ray diffraction (XRD: SmartLab, RIGAKU, Tokyo, Japan) was used as the radiation source with Cu-Kα (λ=1.5405 A°) operated at 40 kV and 40 mA, at the rate of 2θ=1°/min and the glancing angle of 1 was used to investigate the structure phase of the coating layer before and after heat treatment.
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9

Characterization of Coated Biomaterial Samples

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The coated samples morphological evaluation and fractography were investigated by scanning electron microscopy (SEM: JCM-6000 Plus, JEOL, Tokyo, Japan) and field emission scanning electron microscopy (FE-SEM: JSM-7500 FAM, JEOL) at 15kV of accelerating voltage after the gold sputtering. The crystals image was taken by using a STEM-HAADF (JEM-ARM200F, 200 kV, JEOL). X-ray diffraction (XRD: SmartLab, RIGAKU, Tokyo, Japan) with the Cu-Kα (λ=1.5405 A°) at 40 kV and 40 mA was used to investigate the phase of the untreated and coated specimens with BG coating layer. Chemical composition of the prepared BG in this study was investigated using X-ray fluorescence spectroscopy-energy dispersive X-ray spectrometry (XRF, EDX-800HS, Shimadzu, Kyoto, Japan).
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