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Quantaurus qy absolute pl quantum yield spectrometer

Manufactured by Hamamatsu Photonics
Sourced in Japan

The Quantaurus-QY is an absolute photoluminescence (PL) quantum yield spectrometer manufactured by Hamamatsu Photonics. The core function of the Quantaurus-QY is to precisely measure the absolute quantum yield of photoluminescent samples.

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12 protocols using quantaurus qy absolute pl quantum yield spectrometer

1

Synthesis and Characterization of Thiophene-Pyrrole Dyes

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2,4-Dimethylpyrrole
(≥ 97.0, Sigma-Aldrich), 4-bromobenzaldehyde (≥ 99.0,
Sigma-Aldrich), trifluoroacetic acid (≥ 99.0, Sigma-Aldrich),
DDQ (≥ 98.0, Sigma-Aldrich), boron trifluoride diethyl etherate
(≥ 98.0, TCI), 5-formyl-2-thienylboronic acid (≥ 95.0,
Sigma-Aldrich), bis(triphenylphosphine)palladium(II) dichloride (≥
98.0, Sigma-Aldrich), n-hexane (HPLC grade, ≥ 99.0, Sigma-Aldrich),
dichloromethane (anhydrous, ≥ 99.9, Sigma-Aldrich), acetonitrile
(anhydrous, ≥ 99.9, Sigma-Aldrich), ethanol (≥ 99.8,
Sigma-Aldrich), chloroform (≥ 99.8, Sigma-Aldrich), and ethyl
acetate (anhydrous, ≥ 99.8, Sigma-Aldrich) were used. All metal
salts were used as their water-soluble sulfate, nitrate, or chloride
salts, purchased from Sigma-Aldrich (≥ 95). A Varian VNMRJ
600 nuclear magnetic resonance spectrometer was used for 1H NMR and 13C NMR measurements. Mass analysis was conducted
with a Thermo Q-Exactive Orbitrap device. Ultraviolet–visible
(UV–vis) absorption spectra were obtained with a spectrophotometer
(Shimadzu 1900i). Fluorescence emission measurements were obtained
using a Varian Cary Eclipse fluorescence spectrophotometer. Quantum
yield measurements were conducted with a Hamamatsu Quantaurus-QY absolute
PL quantum yield spectrometer.
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2

Thermal Deposition of Ir(III) Complexes

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Samples were fabricated by thermal deposition for 50-nm-thick film on fused silica substrates under a high vacuum of 10−8 Torr. The four Ir(III) complexes were doped at a 2 wt% level in a DP-BCZ:PTZP-PCZ host. PL spectra and PL quantum yield of the film samples were measured using Quantaurus-QY absolute PL quantum yield spectrometer (C11347-11, Hamamatsu) and excitation wavelength of 340 nm was used. Time‐resolved PL characteristics for decay time of the Ir(III) complexes were measured using time-correlated single photon counting (TCSPC) setup (Fluotime 300, PicoQuant GmbH). The samples were excited by a pulsed LED (PLS 340, PicoQuant GmbH, 0.25 MHz repetition rate at 340 nm). Angle-dependent PL spectra for calculation of transition dipole moment orientation was measured by Luxol-OLED Analyzer (CoCoLink Korea). The basic principle of this experimental equipment and the measuring method of the angle-dependent PL spectra follow the standard protocol reported previously6 (link),23 (link). The horizontal transition dipole moment was calculated using the associated fitting software.
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3

Comprehensive Spectroscopic Characterization of Nanomaterials

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UV-vis absorption spectra and Photoluminescence (PL) spectra were recorded by a Cary-60 UV-vis spectrophotometer and an F-380 fluorescence spectrometer (Tianjin Gangdong Sci. & Tech. Development Co., Ltd., Tianjin, China), respectively. The high-resolution transmission electron microscope (HRTEM) images and energy dispersive X-ray spectroscopy (EDX) analysis were characterized using the FEI Talos F200X TEM instruments operated at an accelerating voltage of 200 kV. X-ray powder diffraction (XRD) patterns of samples were performed on a Bruker D8 Advance X-ray Diffractometer at 40 kV and 40 mA using Cu Kαradiation (λ = 1.5406 Å). The photoluminescence quantum yield was obtained using an integrating sphere with a Hamamatsu Quantaurus-QY Absolute PL quantum yield spectrometer (Model: C11347-11). X-ray photoelectron spectroscopy (XPS) analysis was recorded by a Kratos Axis Ultra-DLD spectrometer, and all the spectra were calibrated to the C1s peak at 284.8 eV.
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4

Comprehensive Optoelectronic Characterization

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1H and 13C NMR spectra were obtained in CDCl3 with a Bruker Biospin Avance-III 500 NMR (Germany) spectrometer at ambient temperature. Absorption, PL, and phosphorescence spectra were measured using a UV–Vis spectrometer (Lambda 950; Perkin-Elmer, United states), a spectrofluorometer (FluoroMax-3, Horiba, Japan), and another spectrofluorometer (FP-8600, JASCO, Japan), respectively. Absolute PL quantum yields were measured using a Quantaurus-QY absolute PL quantum yield spectrometer (C11347-11; Hamamatsu Photonics, Japan) under 360-nm excitation and an Ar flow. The thicknesses of the materials were measured by variable angle spectroscopic ellipsometry (M-2000U; J. A. Woollam Co., Inc., United states). Transient PL decay curves were measured using a Quantaurus-Tau fluorescence lifetime measurement system (C11367-03; Hamamatsu Photonics, Japan).
EL spectra, JV characteristics, and ηEQEJ characteristics were measured using an absolute EQE measurement system (C9920-12, Hamamatsu Photonics, Japan). Transient EL characteristics were measured using a photomultiplier tube (R928; Hamamatsu Photonics, Japan) connected to an amplifier unit (C6438; Hamamatsu Photonics, Japan) under pulsed driving using a pulse generator (8114A; Agilent, United states). Signals were monitored using an oscilloscope (TBS2104, Tektoronix, United states).
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5

Quantum Yield Measurements Protocol

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Fluorescence quantum yields (absolute values) were obtained on a Quantaurus-QY absolute PL quantum yield spectrometer (model C11347-12, Hamamatsu) at ambient temperature (25 °C), excitation wavelengths were 20 nm shorter than the absorption maxima of the measured compounds; all measurements were performed in triplicates.
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6

Comprehensive Characterization of Perovskite Nanocrystals

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SEM was measured with Verios G4 UC (FEI) and UPS spectra were collected using a photoelectron spectrometer (Thermo FisherScientific Theta Probe) with a He I (21.22 eV) ultraviolet source in Hanyang LNC 3.0 Analytical Equipment Center (Seoul). PLQY measurement was conducted with a Quantaurus‐QY Absolute PL quantum yield spectrometer (HAMAMATSU) equipped with an integrating hemisphere, and samples were excited at the wavelength of 365 nm. Steady‐state PL measurements were carried out using a pulsed xenon lamp. And time‐resolved PL decay measurements were carried out using a He–Cd laser operating at a wavelength of 375 nm. For PeLEDs, J–V–L characteristics and device performances were measured using a Konica Minolta spectroradiometer (CS‐2000) with a Keithley 2450 sourcemeter. XRD patterns were measured using an X'Pert‐MPD diffractometer (Philips, Netherlands) employing CuKα radiation. UV–vis absorption spectra were measured by a V‐770 spectrophotometer (JASCO). TEM samples were prepared by diluted QD solution in hexane dropped on a carbon grid. TEM was measured with the JEM‐2100F model (JEOL). The Fourier transform infrared (FT‐IR) was recorded on PerkinElmer Spectrum Two FT‐IR Spectrometer.
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7

Synthesis and Characterization of Novel Organic Compound

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All reagents were purchased from Sigma-Aldrich and used without further purification. 1H NMR and 13C NMR were measured on a VNMRJ 600 nuclear magnetic resonance spectrometer (Varian Inc., Palo Alto, CA, USA). The mass analysis was conducted with Thermo Q-Exactive Orbitrap device (Thermo Fisher Scientific Inc., Waltham, MA, USA). The melting point was determined by using the Electrothermal Melting Point Apparatus 9200. UV-vis absorption and fluorescence emission spectra were obtained using a Shimadzu 1900i spectrophotometer and Varian Cary Eclipse fluorescence spectrophotometer (Varian Inc.), respectively. Quantum yield measurements were conducted with Hamamatsu Quantaurus-QY Absolute PL quantum yield spectrometer. The pH values were adjusted by using the HI-8014 (HANNA) pH meter.
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8

Synthesis and Characterization of Novel Organic Compound

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All reagents were purchased from Sigma-Aldrich and used without further purification. 1H NMR and 13C NMR were measured on a VNMRJ 600 nuclear magnetic resonance spectrometer (Varian Inc., Palo Alto, CA, USA). The mass analysis was conducted with Thermo Q-Exactive Orbitrap device (Thermo Fisher Scientific Inc., Waltham, MA, USA). The melting point was determined by using the Electrothermal Melting Point Apparatus 9200. UV-vis absorption and fluorescence emission spectra were obtained using a Shimadzu 1900i spectrophotometer and Varian Cary Eclipse fluorescence spectrophotometer (Varian Inc.), respectively. Quantum yield measurements were conducted with Hamamatsu Quantaurus-QY Absolute PL quantum yield spectrometer. The pH values were adjusted by using the HI-8014 (HANNA) pH meter.
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9

Absolute PLQY Measurement of Quantum Dots

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Absolute PLQY was measured by Hamamatsu Quantaurus-QY Absolute PL Quantum Yield Spectrometer in hexane excited at 500 nm. For continuous wave excitation, 532 nm was selected from a Xenon lamp combines with a monochromator. For the stability testing of the QDs film, the power of the light is fixed at 0.2 mW. The temperature dependent PL measurements of the samples were performed between 10 and 300 K within a helium closed-cycle cryostat, and the signal was dispersed by a 750 mm monochromator combined with suitable filters, and detected by a photomultiplier using the standard lock-in amplifier technique. For high density excitation, the laser source was replaced by a frequency-doubled, Q-switched Nd:YAG laser which produced green pulse at the wavelength of 532 nm. The signal was detected by a UV-enhanced charged coupled device (CCD). The pulse width and repetition rate of the laser are about 1 ns and 60 Hz, respectively.
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10

Characterization of Organic Compounds

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1H NMR and 13C NMR spectra were recorded using a Bruker AVANCE III HD 400 MHz nuclear magnetic resonance spectrometer and a Bruker AVANCE III HD 700 MHz nuclear magnetic resonance spectrometer. Absorption spectra were recorded using a PERSEE TU-1950 double-beam UV-vis spectrophotometer at room temperature. Fluorescence emission spectra were recorded using a HITACHI F-7000 fluorescence spectrophotometer. Quantum yield was collected using a QuantaurusQY Absolute PL quantum yield spectrometer, C11347-11|Hamamatsu Photonics. ESI-MS spectra were recorded using a Q-TOF 6520 LC-MS AGILENT instrument. IR spectra were recorded using a Thermo IS5 Fourier transform infrared spectrometer. Elemental analysis was performed using an EA3000 elemental analyzer at the Analysis and Testing Center of Beijing Institute of Technology.
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