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17 protocols using mfp 3d origin

1

Characterization of AuNP Film Morphology

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Sample morphology was analysed using scanning electron microscopy (Hitachi S-5500, 10 kV accelerating voltage) and white light vertical scanning profilometry (Bruker Contour GTK) to obtain heights of monolayer and bilayer AuNP film regions. Atomic force microscopy (Asylum Research MFP-3D Origin+) was also used to characterize layer heights. X-ray photoelectron spectroscopy (ThermoFisher Escalab 250Xi) was used to measure the surface chemistry of MLAgg films using a monochromated Al Kα X-ray source.
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2

Ferroelectric Mapping by SPM

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Both film surface micromorphology and film ferroelectricity were characterized by Asylum Research MFP-3D Origin+ scanning probe microscopy (SPM). Out-of-plane and in-plane ferroelectric polarization were tested by VPFM and LPFM respectively. For PFM measurements, Dual AC resonance tracking (DART) mode was adopted, with ac bias of 2 V applied to Pt/Ir coating Si scanning tips during reading. As for the domain writing process, positive or negative biases (amplitudes vary by film thickness) were applied on the tip when scanning different regions, so as to create designed domain patterns.
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3

Characterization of Stretchable Conductive Inks

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Flat PDMS substrates were made using a similar procedure described in the skin replica fabrication (see the Supplementary Information). The Ag-PEDOT:PSS and P3HT-NF inks were drawn onto the flat PDMS for mechanical characterization. SEM (XL-30S FEG, Philips) and AFM (MFP-3D ORIGIN+, Asylum Research) images were taken to visualize the morphologies and structures of the Ag-PEDOT:PSS and P3HT-NF inks, respectively. I-V characteristics were measured using a semiconductor characterization system (2612B, Keithley). Stretching/releasing tests were performed with a cyclic automatic stretcher (CK-700FET, CKSI Co. Ltd.). A power supply (1627A, BK Precision) was used to apply DC bias to the DoS heater.
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4

Characterization of Silver Nanoparticles and Hydrogels

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The SEM images were taken with a secondary-electron scanning electron microscope (EVO18, ZEISS), and the samples were subjected to supercritical drying and coated with a gold film for 120 s beforehand. The optical microscopy images were obtained using an inverted microscope (DMI 3000B, Leica). The thickness and roughness of the Ag NPs layer were measured by a commercial Atomic Force Microscope (MFP-3D Origin, Asylum Research). The mechanical property (Young’s modulus (E0)) of hydrogels with different components were measured by a Micromechanical Testing System (FemtoTools, FT-MTA02). The rheological properties of the hydrogels were measured by a rotational rheometer (Physical MCR 301, Anton Paar, Austria).
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5

Multimodal Characterization of Crystal Structure and Surface Morphology

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X‐ray diffraction (XRD, Rigaku Smartlab) was used to examine the crystal structure. Atomic force microscopy (AFM, Asylum Research, MFP‐3D Origin+) was used to study the surface morphology. The X‐ray photoelectron spectroscopy (XPS, Thermo Fisher Scientific EscaLab 250) was performed using Al Kα (hv = 1486.6 eV) radiation as the excitation source. Raman spectroscopy was carried out with a HORIBA HR800 Raman microscope with laser excitation at 532 nm.
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6

Multi-Technique Characterization of Materials

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Optical microscope images were captured using a Nikon ECLIPSE Ci microscope. Scanning Electron Microscope (SEM) images were acquired by a JSM-7610F PLUS operating at 1 kV. Transmission Electron Microscope (TEM) images were obtained by a JEOL ARM200F at 200 kV. Crystal structures were analyzed through powder XRD analysis conducted on a Smart lab Rigaku instrument. Height profiles were measured using AFM (Asylum Research MFP-3D Origin) in noncontact mode. Raman spectra were recorded under 532-nm excitation with an output of 10 µW, while PL spectra were recorded under 405 nm excitation with 1 µW, where the laser beam was focused to a spot size of ≈2 µm (Zolix Finder Smart FST2-MPL501-405C1). All photoelectric measurements were performed using a Keithley 2612B instrument. Unless specified otherwise, all the measurements were performed at room temperature.
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7

Magnetic Imaging of Fe3GaTe2 Flakes

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The MFM images of Fe3GaTe2 flakes on a SiO2/Si wafer were measured at room temperature using an Asylum Research MFP-3D Origin+ scanning probe microscope. The zero-field skyrmion lattices were induced by an MFM tip with a strong stray field. A low stray field of MFM tips was used to measure the MFM image to avoid magnetic interactions of the tip with the sample or an applied field. The spatial magnetic resolution was better than 25 nm. We used a two-step method in frequency-modulation mode to measure the MFM images. The distance between the sample surface and the MFM tip was fixed at 50 nm.
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8

Characterization of Receiving Substrates

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SEM images were obtained using a JSM-7600F (JEOL) instrument at an accelerating voltage of 5 kV in lower secondary electron detection mode. The water contact angles and surface free energies were obtained using a contact angle meter (DMo-502, Kyowa Interface Science). The surface free energies of the receiving substrates were calculated using the contact angles of water and diiodomethane, and the theoretical equation by Owens and Wendt55 (link). TGA was performed using a TGA Q50 instrument (TA Instruments) with a Pt pan to hold the sample. The analysis was performed in a closed chamber with an air flow of 40 ml/min at a temperature increase rate of 10 °C/min. The surface roughness and texture were measured using an AFM (MFP-3D Origin, Asylum Research) at a scan rate of 0.2 Hz. The adhesion forces of the receiving substrates were measured using an ENT-5X instrument (ELIONIX Inc.) at a stage speed of 200 nm/s and load step of 1 µN (20 ms intervals).
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9

Graphene Topography Characterization with AFM

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AFM (MFP-3D Origin, Oxford Instruments) in the tapping mode with 268 scan lines and 268 scan points with a scan rate of 0.10 Hz was used to capture the topography of the graphene layer over a large area (Fig. 1d).
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10

AFM Characterization of ACC-CNFs

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At each treatment step, the size and morphology of the ACC-CNFs were observed by AFM (MFP-3D Origin; Oxford Instruments Asylum Research, Inc., Santa Barbara, CA, USA) using a silicon cantilever (OMCL-AC160TS-R3; Olympus Corp., Tokyo, Japan). An aqueous dispersion of CNFs (1.0 × 10 -3 wt%) was dropped onto a cleaved natural mica substrate (The Nilaco Corp., Tokyo, Japan), then dried at room temperature. The AFM measurements were operated in AC mode under ambient conditions.
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