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11 protocols using quantaurus tau

1

Fluorescence Lifetime Analysis of ANA Variants

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Fluorescence lifetime of ANA variants (1 μM) were measured using a fluorescence lifetime spectrometer Quantaurus-Tau (Hamamatsu Photonics). In all measurements, the excitation wavelength was 470 nm and fluorescence emissions were determined at 538 nm. Fluorescence lifetimes were then calculated using a single exponential curve fitting (protoANA1 and protoANA2) or double exponential fit (ANA-Y).
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2

Photophysical Properties of Luminescent Compounds

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UV–vis
absorption spectra
were detected using a JASCO V-550 absorption spectrometer. A Hitachi
F-7000 fluorescence spectrometer equipped with a Hamamatsu R928 photomultiplier
detector was used to record the steady-state photoluminescence spectra.
Φem were measured in powder form using a calibrated
integrating sphere (Hitachi). The powder luminescence behavior at
various temperatures was investigated by placing it in a thin quartz
cell (1 × 10 × 20 mm) set on a homemade heating stage. The
decay patterns and emission lifetimes of 11 and 12 were measured at λ = 545 and 477 nm, respectively,
using a Quantaurus-Tau photoluminescence lifetime measurement device
(C1136-21, Hamamatsu) with λex = 340.
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3

Fluorescence Lifetime Measurements Protocol

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Fluorescence lifetime measurements with a low time resolution of 1 ns were conducted using a fluorescence lifetime measurement system (Quantaurus-Tau, C11367-03, Hamamatsu Photonics, Hamamatsu, Japan) at 20 °C. The decay component was recorded using excitation by applying a flashing light-emitting diode (LED) light at a wavelength of 340 nm. The fluorescence decay curves accumulated until the peak intensity reached 1000. The emission decay data were well-fitted using one to three exponentials using the deconvolution method. The lifetimes τi were determined as fitting parameters so that the χ2 value would be in the range of 1.00 ~ 1.18. Here, χ2 is an indicator for the degree of fitting and defined as χ2=j=n1n2ItjFtj2Itj/n2n1+1 , where I(tj) is a calculated value for each channel, and n1 and n2 are the first and last channels in the analysis range. The residual value defined as rtj=ItjFtjItj was within ±5% for all the fitting curves. Thus, the error of τ is estimated to be at most ±0.5 ns. The average lifetime was calculated as τ=i=1nAiτi2/i=1nAiτi , where Ai is the pre-exponential lifetime τi .
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4

Fluorescence Lifetime Measurement Protocol

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Fluorescence lifetime measurements
with a lower time resolution
of 1 ns were conducted using a fluorescence lifetime measurement system
(Quantaurus-Tau, C11367–03, Hamamatsu Photonics, Japan) at
room temperature. The decay component was recorded using excitation
by applying a flashing light-emitting diode (LED) light at a wavelength
of 340 nm. Fluorescence decay curves were accumulated until the peak
intensity reached 1000. The phosphorescence lifetimes were measured
using a xenon flash lamp unit (C11567-02, Hamamatsu). The decay component
was recorded under excitation using a band pass filter (340 ±
10 nm), and phosphorescence decay curves were accumulated for 5 min.
The emission decay was well fitted using one to three exponential
functions. The average lifetime was calculated as ⟨τ⟩
= ∑Ai τi2/∑Ai τi, where Ai is the pre-exponential factor for lifetime τi.
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5

Characterization of Photoactive Compounds

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UV/vis and fluorescence spectra were recorded in a high-pressure cell (path length: 2 mm) by using a JASCO V-650 or a JASCO FP-8500. Fluorescence lifetimes were measured in a high-pressure cell by a Hamamatsu Quantaurus-Tau single photon counting apparatus fitted with an LED light source (λex = 405 nm). Nanosecond transient absorption (nsTA) measurements were performed by using a Unisoku TSP-2000 flash spectrometer-pump pulse source: Surelite-I Nd:YAG (Continuum, 4–6 ns fwhm) laser with the second harmonic at 532 nm, monitor light source: xenon lamp (150 W), and detector: photomultiplier tube. 1H NMR spectrum of Pc-BP-Pc was recorded on an ECS-400 spectrometer.
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6

Optical and Structural Characterization of CsPbBr3 QDs

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The optical absorption and PL spectra were measured for the CsPbBr3 QDs in solution. The absorption spectra were recorded using a ultraviolet–visible–near infrared (UV–Vis–NIR) spectrophotometer (Agilent technologies, Cary 5000, Santa Clara, CA, USA). The PL spectra were carried out using an absolute PLQY spectrometer (Hamamatsu photonics, Quantaurus-QY, Hamamatsu, Japan) under UV (400 nm) illumination with a 150 W xenon lamp. The time-resolved PL decay was recorded using Fluorescence lifetime analysis (Hamamatsu photonics, Quantaurus-tau, Hamamatsu, Japan) equipped with a 405 nm, 200 kHz pulse. The high-resolution transmission electron microscope (HRTEM) image of QDs were obtained using Hitachi, HF-3300. Samples for TEM were prepared by dropping of the CsPbBr3 QDs in toluene onto a carbon-coated 300 mesh copper grid with support films. The X-ray diffraction (XRD) measurements were carried out using Panalytical, X’pert-PRO (Almelo, Netherlands). For the XRD measurements, the solution of CsPbBr3 QDs were dropped into a cleaned glass, and then dried at room temperature for 30 min. The HOMO level were measured by UV photoelectron spectroscopy (UPS) using ULVAC-PHI. The x-ray photoelectron spectroscopy (XPS) measurements were conducted employing PHI 5000 Versa Probe II.
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7

Characterization of Organic Polymers

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Melting points were measured by a Büchi M-560 apparatus. HRMS spectra were recorded on a Bruker ESI microTOF II instrument. 1H, 13C, 2D-COSY, and -HMQC NMR spectra (400 or 100 MHz) were measured in CDCl3 containing tetramethylsilane (TMS) as an internal standard with an ECX400 NMR spectrometer. UV/vis spectra were measured in a quartz cell (1 cm path length) by recording on a JASCO V-650 spectrometer equipped with an ETCS-761 temperature controller. Fluorescence spectra were measured in the same cell using a JASCO FP-8500 spectrophotometer equipped with an ETC-815 temperature controller. Fluorescence lifetime decays were observed in the same cell by a Hamamatsu Quantaurus-Tau single-photon-counting instrument fitted with an LED excitation light (340 nm). IR spectra were measured on a JASCO FT/IR-4700 spectrometer. The molecular weights of the PTs were determined using polystyrene standards through an analytical GPC with a TOSOH TSKgel α-4000 column (condition: 40 °C, 0.5 mL min−1, DMF).
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8

Optical Characterization of Glass Specimens

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Transmittance spectra of the glass specimens were measured using a spectrophotometer (V670, JASCO) across a spectral range from 190 to 2700 nm with 1 nm intervals. The PL excitation/emission spectra were measured by a spectrofluorometer (FP-8600, JASCO) which equipped a Xe-lamp. The range of monitored wavelength was from 300 to 600 nm while the excitation wavelength was 260 nm. Excitation spectra was measured from 200 to 350 nm when the monitored wavelength was 440 nm. PL QYs were measured using Quantaurus-QY (C11347, Hamamatsu Photonics) at R.T. QY includes the measurement errors in ± 2%. The monitored excitation/emission wavelength ranges were 250–350 and 350–750 nm with 10 nm intervals, respectively. To determine an origin of luminescence, PL lifetime measurements were performed using Quantaurus-Tau (C11367, Hamamatsu Photonics).
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9

Spectroscopic Characterization of Glass

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The Tg was determined by differential thermal analysis at a heating rate of 10 °C/min using a TG8120 (Rigaku). The PL and PLE spectra were measured at room temperature using an F9000 fluorescence spectrophotometer (Hitachi). The absorption spectra were measured at room temperature using a U3500 spectrophotometer (Hitachi). The emissions decay at room temperature was measured using a Quantaurus-Tau (Hamamatsu Photonics) whose excitation light source was a 4.43-eV (280-nm) LED operated at a frequency of 10 kHz. The photoluminescence dynamics were also evaluated using a streak camera and a monochromator. The light source used for photoexcitation was an optical parametric amplifier system based on a regenerative amplified mode-locked Ti:sapphire laser (Spectra Physics) with a pulse-duration of 150 fs and a repetition rate of 1 kHz. The absolute QY of the glass was measured using a Quantaurus-QY (Hamamatsu Photonics).
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10

Scintillator Film Optical Characterization

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The scintillator film PL spectra were excited using a 150-W Xe lamp light and collected by using a FluoroMax+ fluorescence spectrometer of Horiba Scientific, and time-resolved PL spectra were tested using a Quantaurus-Tau (Hamamatsu C11367-31,). UV-vis spectrometer (Shimadzu UV-3600) recorded the absorption spectra in the wavelength range from 250 to 650 nm. To explore the transmittance of scintillator films and quartz, a fiber optical spectrometer (Idea optics PG 2000) and integrated sphere combination were carried out. An FDTD method was carried out to simulate the situation in light spread in quartz. The luminescence of scintillation is set as Gaussian light, and the model is approximately reduced to 10−4 of the actual situation (fig. S7).
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