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Evolution 220 spectrometer

Manufactured by Thermo Fisher Scientific

The Evolution-220 spectrometer is a versatile laboratory instrument designed for precise spectroscopic analysis. It features a wide wavelength range and high-resolution optics to accurately measure the absorption or emission properties of samples. The core function of the Evolution-220 is to quantify the spectral characteristics of materials, enabling researchers and analysts to identify and study the composition of a wide variety of substances.

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4 protocols using evolution 220 spectrometer

1

Detailed Characterization of Electrochemical Reagents

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Example 1

Dowex 50WX4, zinc acetate dihydrate and tetramethylammonium hydroxide were purchased from Acros organics. Bromoacetic acid, hydroxylamine hydrochloride, calcium chloride and hydrochloric acid were purchased from Alfa Aesar. Vanadyl bis-acetylacetonate and ferrocene were purchased from Strem chemicals and 2-propanol and dimethylsulfoxide were purchased from Fisher Scientific. All reagents and solvents were used without purification except DMSO, which was distilled over 4 A molecular sieves and degassed, and ferrocene, which was sublimated prior to use in electrochemical experiments. Tetrabutylammonium hexafluorophosphate was purchased from Alfa Aesar, recrystallized 3× from ethanol and water, and dried at 55° C. under vacuum prior to use in electrochemical experiments. Tetraethylammonium hexafluorophosphate was purchased from Alfa Aesar, recrystallized 3×, from water and dried at 55° C. under vacuum before use.

Infrared Spectroscopy was performed with a ThermoFisher is5 using an ATR attachment. UV-vis spectra were measured using a ThermoFisher Evolution 220 spectrometer. Static cell electrochemical experiments and cyclic voltammetry was carried using a Princeton Applied Research Versastat 3 potentiostat. X-ray crystallography was carried out with a Bruker D8 Venture X-ray instrument. NMR spectroscopy was carried out using a 400 MHz Bruker Advance III spectrometer.

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2

Characterization of [Fe(DPA-Bpy)(NCCH3)](OTf)2 Complex

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1H NMR spectra were measured by the Bruker 500 MHz NMR spectrometer. Elemental analysis of the [Fe(DPA-Bpy)(NCCH3)](OTf)2 complex was conducted by Atlantic Microlab, Inc., Atlanta, Georgia. The mass spectra were obtained by the Thermo Q Exactive field and Bruker Ultraflex MALDI-TOF MS spectrometer. UV–Vis spectra were recorded on a Thermo Evolution-220 spectrometer. Fluorescence spectra were recorded on a FluoroMax-4 spectrofluorometer.
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3

Characterization of TiO2 Nanotubes Photocatalysts

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A Phenom ProX Scanning Electron Microscope (SEM) equipped with EDS was used to study the morphology and structure of the TiO2NTs-based photocatalysts.
A D2 Phaser Bruker diffractometer equipped with a Ni β-filtered Cu-Kα radiation source was used to investigate the phase composition of the catalysts. In detail, data were collected in a 2θ range from 20° to 60° at a scanning rate of 0.025° s−1. The JCPDS database of reference compounds was used to identify the diffraction peaks.
Ultraviolet–visible diffuse reflectance spectra were recorded with a Thermo Fisher Evolution (220) spectrometer with an integrating sphere for solid samples. The light-harvesting characteristics of the photoactive materials were determined using a spectroradiometer (Lot Oriel, model ILT950, Quantum Design Europe, Darmstadt, Germany)
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4

Comprehensive Analytical Techniques for Chemical Characterization

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1H NMR spectra were measured by Bruker 600 MHz nuclear magnetic resonance spectrometer. Mass spectra were obtained by Thermo Q Exactive field orbital well cyclotron resonance mass spectrometer. IR spectra (solid infrared, liquid infrared and time-resolved infrared) were carried out by Thermo Nicolet iS50 FT-IR infrared spectrometer. UV-vis spectra were measured by a Thermo Evolution-220 spectrometer. Elemental analysis was measured by a vario EL CUBE. XRD was conducted by a Bruker Smart Apex II diffractometer. EPR was measured by a Bruker EMXPLUS10/12 spectrometer. Fluorescence spectra were measured by a FluoroMax-4 spectrofluorometer. The molecular weight of protein was analyzed by Bruker Ultraflex MALDI-TOF-MS spectrometer. Agarose gel electrophoresis was performed by DYY-6C electrophoresis apparatus of Beijing Liuyi Biological Technology Co., Ltd (Beijing, China). A cytotoxicity test was measured by SpectraMax iD5 microplate reader. Confocal microscopy images were analyzed by a LSM-880 confocal laser scanning microscope.
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