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Su6600

Manufactured by JEOL
Sourced in Japan

The SU6600 is a field emission scanning electron microscope (FE-SEM) manufactured by JEOL. It provides high-resolution imaging capabilities for a wide range of applications. The SU6600 utilizes a cold field emission gun to generate a stable and high-brightness electron beam, enabling detailed observation of samples at the nanoscale level.

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2 protocols using su6600

1

Characterization of Amphiphile-Templated Gold Nanoparticles

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The morphologies of self-assembled
amphiphiles before and after the interaction of HAuCl4 were
obtained from SEM (Hitachi S-3000N, Japan) and FESEM (Hitachi High
Tech SU6600), and high-resolution transmission electron microscopic
(HRTEM) images were recorded with a JEOL JEM 2100 microscope equipped
with a Gatan imaging filter. Samples for SEM and FESEM imaging were
prepared by casting 5–10 μL of amphiphile-templated AuNPs
on aluminum foils and then were dried at ambient temperature. The
HRTEM analysis was conducted by placing a drop of the NP solution
on a carbon-coated copper grid and followed by solvent evaporation
under ambient temperature. The average size of the NPs was analyzed
using ImageJ software.
For optical microscopic studies, the
glass slides were initially washed with alcohol and then with double-distilled
water and were dried in a hot air oven. The amphiphile-templated AuNPs
were dropped onto a glass slide using a micropipette and were allowed
for slow evaporation at ambient temperature. The resulting dried drops
were imaged on a Leica DM 2500 optical microscope.
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2

Characterization of Graphene Oxide and Manganese Oxide Composite Fibers

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The morphological characteristics of rGO, synthesized MnO2 nanoparticles and composite fibers of MnO2 + rGO + PAN (rGOMnPAN) were studied using SEM (Hitachi SU 6600) and TEM (JEOL JEM 2100 HRTEM). Both MnO2 nanoparticles and rGO were further analyzed using XPS (Thermo Fischer ESCALAB Xi+ with Al-Kα radiation). Raman spectroscopy (Bruker Senterra) of rGO was also carried out using a 532 nm wavelength in order to obtain more details about the chemical structure. XRD (Bruker D8 FOCUS with Cu-Kα radiation with X-ray operating at 25 kV and 30 mA) analyses were performed for all materials in order to obtain an idea about the fiber constituents and crystallinity. EDX (Ametek-EDAX EDX detector) analyses were also carried out to ensure the incorporation of the nanomaterial within the fiber structures. The surface area and the total pore volume of the C-rGOMnPAN material were investigated by N2 adsorption at 77 K (Quantachrome Autosorb iQ Surface Area Analyzer). The sample was degassed at 120 °C for 30 min prior to analysis. To understand the hydrophilic/hydrophobic nature of the electrospun electrode material, the time to completely absorb a known amount (50 and 100 μL added using a micropipette) of distilled water by fiber mats with known thicknesses (thickness measured using a thickness gauge – SYLVAC μs229) were measured.
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