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Vertex v70 spectrometer

Manufactured by Bruker

The Vertex V70 spectrometer is a Fourier-transform infrared (FTIR) spectrometer designed for a variety of analytical applications. It features a high-performance interferometer and a sensitive detector to acquire infrared spectra of solid, liquid, and gaseous samples. The core function of the Vertex V70 is to provide accurate and reliable infrared spectroscopic data for research, quality control, and other analytical purposes.

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4 protocols using vertex v70 spectrometer

1

Structural Analysis of POC Polymers

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To check the chemical structural difference between POC, POC-βGP-Na and POC-GP-Ca, Fourier transform infrared (FT-IR) analysis was operated by casting polymer solution in 1,4-dioxane on KBr pellets using Bruker Vertex V70 spectrometer. FT-IR spectra were recorded over a wavelength range of 400-4000 cm. 31P NMR (161.9 MHz) spectra of pre-polymer solutions were obtained using Bruker DPX 400 NMR Spectroscopy. Either D2O or DMSO were used as solvents. All chemical shifts were reported in ppm (δ).
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2

Comprehensive Material Characterization

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The morphologies and elemental components of the samples were characterized by SEM (Hitachi SU8020) and TEM (JEOL JEM‐2100F) equipped with energy dispersive spectrometry (EDS) at an acceleration voltage of 200 kV, respectively. The XRD patterns were recorded on an X‐ray diffractometer at 40 kV and 40 mA using Cu Kα radiation (Bruker D8 Advance). XPS spectra were collected on the ESCALAB 250Xi, (Thermo Fisher Scientific Inc., USA) equipped with Ar ion etching (2 kV; 2 µA). To obtain Brunauer–Emmett–Teller (BET) specific surface areas of the materials, nitrogen adsorption–desorption isotherms were recorded by nitrogen adsorption apparatus (ASAP2020, Micromeritics). FTIR characterization was carried out on a Bruker Vertex V70 spectrometer in the diffuse reflection mode with a Spectra Tech Collector II accessory. Depth profiling and chemical analysis data of the sample were collected on a TOF‐SIMS instrument (IONTOF GmbH, Germany 2010). The data were recorded in ultrahigh vacuum at a pressure of 10−9 Torr in a negative model.
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3

Comprehensive Nanoparticle Characterization Protocol

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Transmission electron microscopy (TEM) and scanning electron microscopy images were observed by JEOL TEM-1210 operated under 120 kV and EX-250 SEM (horiba), Respectively. The phase of nanoparticles were recorded on a D8 Focus diffractometer (Bruker) with Cu Kα radiation (λ = 0.15405 nm). Fourier transform infrared (FTIR) spectra were examined on a Bruker VERTEX V70 spectrometer with the range of 500-4000 cm-1. Nitrogen (N2) adsorption desorption isotherms curves and the corresponding pore-size distributions were obtained using a TriStar 3000 (Micromeritics, Norcross, GA, USA) surface area analyzer. The size distribution and zeta potential was performed on a Zetasizer Nano ZS particle analyzer (Malvern Instruments Limited). The CD spectra of the samples were measured by a chirascan-plus spectropolarimeter (Applied Photophysics, UK). The fluorescence spectra were analyzed on a 970CRT spectrophotometer. The concerntration of Lapa were carried on high-performance liquid chromatography (HPLC, Agilent 1200, USA). HPLC was performed on a C18 column (Zorbax Eclipse XDB, 4.6 × 150 mm, 5 μm).
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4

Characterization of Battery SEI Layers

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SEM observations were performed on SEM (Nano630 FE-SEM). FT-IR was performed on a Bruker Vertex V70 spectrometer in diffuse reflection mode with a Spectra Tech Collector II accessory. XPS measurements were carried out with a Kratos XSAM800 Ultra spectrometer. 13C NMR characterization was performed on a Bruker AV-3-HD-500. AFM (Digital Instrument Multimode scanning probe microscope) was used to investigate the surface morphology and analyze the mechanical property of the SEI layer under inert atmosphere. The 3D topographic images of SEI layers were recorded through tapping mode imaging with sharp AFM tips (BRUKER TESPA-V2). The scan size was 10 × 10 μm. Another kind of silicon tip (BudgetSensors Multi75Al-G) was employed to test the mechanical behavior of different SEI layers. The spring constants of the AFM cantilevers were calibrated by the Sader method (around 3.2–3.4 N/m)60 (link). All tips were cleaned with UV/ozone to remove organic contaminants. The force-distance curve was obtained from AFM indentation test. The maximum indentation force was kept constant at 150 nN for each test and the vertical probe rate was 316 nm/s. Zygo 3D Optical Surface Profilers were used to investigate the thickness and coverage degree of SEI layers under inert atmosphere. The scan size was 450 × 450 μm.
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