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Icon3

Manufactured by Bruker

The ICON3 is a high-performance benchtop NMR spectrometer designed for a variety of analytical applications. It offers a compact and user-friendly platform for obtaining detailed structural information about molecules. The ICON3 provides robust and reliable performance, ensuring accurate and reliable data acquisition.

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5 protocols using icon3

1

Characterization of MXene@PI Composites

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Scanning electron microscopy (SEM, FEI NanoSEM 230), transmission electron microscopy (TEM, JEOL JEM2200fS) and atomic force microscopy (AFM, Bruker ICON3) were employed to characterize the morphology and microstructure. A drop shape analyzer (DSA 30, Krüss, Germany) was utilized to measure the water contact angles (CA). A FTIR spectrometer (PerkinElmer Spectrum Two) with an attenuated total reflection accessory was used to perform the FTIR measurements. The resistances (R) were measured in a four-probe method by a Keithley 4200 electrometer so as to calculate the electrical conductivity (δ). EMI SE in the frequency range of 8.2–12.4 GHz (X-band) was measured by a vector network analyzer (Agilent 8517A) in the waveguide method. More than three specimens were tested for each component. The S-parameters were recorded and used to calculate the SET, SER, and SEA. To evaluate the electrothermal performance, various DC voltages were applied to the 10L MXene@PI composite foams using a DC-regulated power supply. The temperature of the sample was measured by a digital thermometer (UT325) with its T-type thermocouple contacting the surface of the sample. The electromechanical response of the composite foams was obtained by measuring the resistance change using the Keithley 4200-SCS electrometer in a two-probe method.
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2

Atomic Force Microscopy of Supported Lipid Bilayers

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ScanAsyst-AiIR probes were
used to analyze the topography of the SLs on the Bruker Icon 3 atomic
force microscope.
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3

Cellulose Nanocrystals for Bioapplications

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Cellulose nanocrystals (CNC, prepared via sulfuric acid hydrolysis of bleached softwood kraft pulp, characterized elsewhere 17, 38 ), were purchased in freeze-dried form from CelluForce (Montreal, Canada). CNC (120 ± 61 nm length by 4.0 ± 1.3 nm height, determined via AFM, Bruker ICON3, Supporting Information Figure S1, using FiberApp tracking 39 ) were dispersed in distilled water at 2 wt%, probe sonicated in an ice bath (3 × 10 minute cycles, 60% amplitude, Digital Sonifier 450, Branson Ultrasonics) and stored at 4 ˚C prior to use. Lysozyme from Hen Egg White (HEWL, >90%) was purchased from Sigma Aldrich. Hydrochloric acid and sodium chloride were purchased from VWR Chemicals and used as received.
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4

Multimodal Imaging of Protein Aggregates

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Prior to lap shear testing, all laps were photographed using a digital camera (16 MP resolution). Polarized optical microscopy was performed on selected samples using an Olympus SZX10 microscope, with the illumination, exposure and gain settings remaining unchanged across all images. A slight overexposure enabled the visualization of the fractures, while highlighting differences in birefringence patterns across the samples. Scanning electron microscopy images were recorded using a Zeiss Sigma VP field emission scanning electron microscope at 1.6 kV and working distance of ca. 7 mm. The monomeric HEWLs, their amyloids, and short amyloids were imaged by AFM (Bruker ICON3), with the samples being prepared from ∼0.05 mg mL−1 suspensions deposited on freshly cleaved mica substrates. The ChNCs were imaged by AFM using a JPK-Bruker NanoWizard IV XP on freshly cleaved mica. The length and width of the ChNCs were corrected for tip convolution according to previous work.26 (link)
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5

Tapping Mode AFM Imaging of Worms and Fibrils

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Atomic force microscopy (AFM) imaging (Bruker Icon 3 equipped with Bruker RTESPA-150 probes) in tapping mode was performed on samples of worms (0.01 mg/mL) and amyloid fibrils (0.1 mg/mL) on freshly cleaved mica at a resolution of 1024x1024 lines and at a scan rate of 0.5 Hz. Images were flattened with the Bruker Nanoscope software.
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