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Tecani g2 f20

Manufactured by Thermo Fisher Scientific
Sourced in Japan, United States

The Tecani G2 F20 is a benchtop centrifuge designed for general laboratory applications. It features a maximum speed of 20,000 rpm and a maximum RCF of 48,400 x g. The centrifuge accommodates various rotor options to handle a range of sample volumes and tube types.

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5 protocols using tecani g2 f20

1

Characterization of Carbon Dots via TG-MS, TEM, UV-Vis, Fluorescence, and XPS

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The sample was pyrolyzed by using the model (Japanese Science, thermo plus EV2/ thermo mass photo) Thermogravimetry-Mass Spectrometer (TG-MS) to analyze the experiment. Transmission electron microscopy (TEM) was carried out using an FEI Tecani G2 F20 operating at an acceleration voltage of 200 kV. UV-vis spectra were recorded with a Shimadzu UV-2600 spectrometer. Fluorescence measurements were collected using a Shimadzu fluorescence spectrophotometer RF-6000. QYs of the obtained three CDs were determined by a relative method. X-ray photoelectron spectroscopy (XPS) was investigated by using K-Alpha spectrometer with a mono X-Ray source Al Kα excitation (1486.6 eV). Binding energy calibration was based on C1s at 284.7 eV. HORIBA Scientific LabRAM HR Evolutio was used for Raman analysis. QYs of the obtained three CDs were determined by a relative method. Specially, quinine sulfate (QY = 55% in 0.1 M H2SO4) was selected as the reference for the blue emission, rhodamine 6G (QY = 95% in ethanol) for the green emission, and rhodamine B (QY = 56% in ethanol) for the red emission.
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2

Comprehensive Characterization of Nanomaterials

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Utilising an FEI Tecani G2 F20 working at an acceleration voltage of 200 kV, Transmission electron microscopy (TEM) pictures were captured (The Electronics Corporation, Japan). A Shimadzu UV-2600 spectrometre was used to record UV-vis spectra (Shimadzu Experimental Equipment Co., Ltd., Shanghai, China). Using a Shimadzu RF-6000 fluorescence spectrophotometre, fluorescence measurements were taken (Shimadzu Experimental Equipment Co., Ltd., Shanghai, China). The Thermal Scientific Nicolet iS5 spectrometre was used to acquire the Fourier transform infrared (FT-IR) spectra in transmission mode using the KBr pellet technique (Thermo Fisher Scientific Corporation, Waltham, MA, USA). Utilising a K-Alpha spectrometre with a single X-ray source and Al K excitation, X-ray photoelectron spectroscopy (XPS) was studied. Based on C1s at 284.7 eV, binding energy calibration was performed (Thermo Fisher Scientific Corporation, USA). The samples were excited by a 290 nm (<1 ns) and a 485 nm (200 ps) nano-LED light source. A KONICA MINOLTA CS-150 colourimetre was used to measure the CIE chromaticity coordinate. PL lifetime and QY were measured using FL3-111 (Horiba Scientific, Edison, NJ, USA).
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3

Comprehensive Characterization of Nanoparticles

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PL spectra were measured using a Shimadzu fluorescence spectrophotometer RF-6000 (Shimadzu, Tokyo, Japan). UV-vis spectra was collected with a Shimadzu UV-2600 spectrometer (Shimadzu, Tokyo, Japan). Transmission electron microscope (TEM) image of FEI Tecani G2 F20 (FEI, Hillsboro, OR, USA) measured at 200 kV accelerated voltage operation. Nanosecond fluorescence lifetime was measured by the time-correlated single photon counting (TCSPC) system (HORIBA Scientific iHR 320, Paris, France). Fourier transform infrared (FTIR) spectroscopy was achieved using a Thermo Scientific Nicolet iS5 spectrometer (Thermo Fisher Scientific, Waltham, MA, USA). X-ray photoelectron spectroscopy (XPS) was collected by K-alpha spectrometer (Thermo Fisher Scientific, Waltham, MA, USA). KONICA MINOLTA CS-150 colorimeter (Konica Minolta, Tokyo, Japan) was used to calibrate CIE colorimeter coordinates. Quantum yield (QY) was measured using an FLS1000 spectrometer (Techcomp, Livingston, Edinburgh, UK) equipped with a calibrated integrating sphere.
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4

Facile Synthesis and Characterization of Luminescent Carbon Dots

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CDs were prepared by directly pyrolyzing citric acid (Figure 1). Briefly, 1 gr of anhydrous citric acid was heated at specific temperatures for defined incubation times. The liquid changed from colorless to dark brown, implying the formation of CDs. Then, all samples were neutralized using a 0.5 M NaOH solution to a pH of 7.0. Samples were assigned to four groups based on the temperature and incubation time, i.e., 220-20, 200-30, 180- 40, and 160-50, where the first number in each pair shows temperature in degrees Celsius and the second number shows incubation time in minutes. Dynamic light scattering (DLS) was used to measure CDs particle size. Zeta potential of the CDs was determined using ZEN 3600 (Malvern Instruments Co., USA) for different formation samples. The identification of functional groups was done using a Bruker, Tensor27, FT-IR. To confirm morphological characteristics of the particles, scanning transmission electron microscopy (Tecani™ G2 F20, FEI Company) was used at 200 kV.

Synthetic production of CDs. Carbon dots with high yield were directly synthesized by pyrolizing citric acid in different time and temperature range. The CDs possess bright blue luminescence.

Figure 1
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5

Characterizing Carbon Dots via Spectroscopy

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The conspicuous pictures of transmission electron microscopy (TEM) were captured utilizing an FEI Tecani G2 F20 operating at an acceleration voltage of 200 kV. A Shimadzu UV-2600 spectrometer was used to record the CDs’ UV-Vis spectra. Measurements of fluorescence were conducted using a Shimadzu RF-6000 fluorescence spectrophotometer. Via the KBr pellet method, the Fourier transform infrared (FT-IR) spectrum was acquired under transmission mode using a Thermal Scientific Nicolet iS5 spectrometer. X-ray photoelectron spectroscopy (XPS) was obtained using an Al K excitation K-Alpha spectrometer with a single X-ray source. Binding energy calibration was performed based on C 1s at 284.7 eV. A 290 nm (<1 ns) and a 485 nm (200 ps) nano-LED light source was used to excite the samples. The CIE chromaticity coordinates were measured using a KONICA MINOLTA CS-150 colorimeter. Absolute quantum yield (QY) measurements were performed using a FLS1000 spectrometer (Techcomp, Livingston, Edinburgh, UK) equipped with a calibrated integrating sphere. As the QY was determined by the ratio between photons emitted and absorbed by CDs, it was desirable to place the ethanol solution of CDs in a cuvette to measure their QY, while using solvent ethanol as a blank sample for the reference measurement.
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