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Istar

Manufactured by Oxford Instruments
Sourced in United Kingdom

The IStar is a high-performance scientific instrument designed for advanced imaging and spectroscopy applications. It features a high-speed, low-noise, and back-illuminated CCD sensor that provides excellent sensitivity and dynamic range. The IStar is capable of capturing images and spectra with high spatial and temporal resolution, making it a versatile tool for a wide range of research and industrial applications.

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5 protocols using istar

1

Time-Resolved Fluorescence Spectroscopy

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All samples were placed
into a nonluminescent cell mounted
in a home-built liquid-nitrogen-cooled dewar whose bottom was made
of quartz. The samples were cooled to 77 K to increase the signal
intensity. Dried air was blown over the outside of the quartz windows
to avoid ice formation. The excitation pulse used was the fourth harmonic
generation of a Nd/YAG laser (Quanta Ray, Spectra Physics) coupled
with an optical parametric oscillator unit (Versa Scan and UV Scan)
to convert the wavelength of the laser light to 394 nm. The fluorescence
of the sample was collected at a right angle to the excitation beam
and directed via two lenses into the entrance slit of the spectrometer
(Shamrock RS 303i, 300 lines/mm, Andor Technology). The optically
triggered signals from the PIN photodiode to the controller in the
PC software were adjusted through a delay generator (DG535, Stanford
Research Inc.). The resultant spectra were recorded with a time-gated
ICCD camera (iStar, Andor Technology). The gate width was 25, 50,
or 100 μs, and the delay time after the excitation laser pulse
was 10 μs. Lifetime data were analyzed using the Origin (Light
Stone) software. Details on the detection system can be found in recent
refs.20 (link),22 (link)
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2

Time-Resolved Luminescence Spectroscopy of Eu(III) Complexes

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Time-resolved luminescence spectra were acquired using a nanosecond-pulsed Nd:YAG laser-pumped OPO (Vibrant B, Opotek Inc.) as an excitation source at 394 nm (0.4–1.0 mJ). Dried solid powders were placed in quartz cells (1 mm × 10 mm) and tilted by ∼30° to the incident excitation laser beam path. Emissions were collected using a fiber bundle connected to a spectrograph (SR-303i, Andor Technology). An intensified CCD (ICCD) (iStar, Andor Technology) was used as the detector and its insertion delay time was managed relative to the incident laser pulse.26 (link) A long-path filter (500 nm cutoff) was placed in front of the detector to protect it from the scattered excitation light. The ICCD was set with a gate width of 5 ms and a gain of 1. Spectra were collected by accumulating luminescence signals from 100 excitation bursts. A grating of 600 lines per mm was mainly employed with a slit width of 10 μm.
Luminescence lifetimes, the inverse of the decay rate (τ = 1/kobs), were measured using the kinetic mode of the ICCD with a series of delayed gate openings from the burst of the incident laser pulses. The inner-sphere hydration number (N(H2O)) of the Eu(iii) ion was calculated based on its established relationship with the luminescence lifetime (τ), as expressed in eqn (1).27,28 (link)
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3

LIBS Analysis of Thin Film Samples

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LIBS spectra were acquired using a MobiLIBS system (IVEA, Paris, France). The instrumentation consisted of the pulsed Nd:YAG laser (Quantel, Lannion, France), the Mechelle 5000 Echelle spectrometer (Andor Technology, Ltd., Belfast, Northern Ireland), and the intensified charge coupled device camera (iStar, Andor Technology, Ltd., Belfast, Northern lreland). The spectral region was 200–1000 nm. Every film was shot 25 times according to the 5 × 5 matrices, and the average spectra were obtained. The distance between two points in the matrices was 0.5 mm.
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4

Elemental Analysis of Frozen Tumor Samples

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Frozen tumor samples were cut into 7 μm-thick sections before mounting onto plastic slides. The samples were analyzed with a LIBS system to determine their elemental composition, i.e., boron (B (I) 208.8 nm) and phosphorus (P (I) 214.9 nm) elements in our case. The homemade LIBS setup was based on an optical microscope that combined a LIBS laser injection line, a standard optical-imaging apparatus, and a three-dimensional motorized platform for sample positioning [45 (link)]. In brief, the ablation was created using a quadruple Nd:YAG laser pulses of 1064 nm. The pulse duration was 8 ns, the pulse energy 1 mJ, and the repetition rate 100 Hz. During the sample scan, the objective to sample distance was carefully controlled to compensate for any flatness anomalies. The light emitted by the plasma was collected and connected by an optical fiber to a Czerny-Turner spectrometer equipped with an intensified charge-coupled device camera (Shamrock 303 and iStar, Andor Technology, Belfast, UK). The experiments were performed by Ablatom S.A.S.
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5

Laser-Induced Breakdown Spectroscopy for Material Analysis

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A MobiLIBS system (IVEA, France) was used for laser-induced breakdown spectroscopy (LIBS) to determine the atomic composition and content of the material samples. The system consisted of a fourth-harmonic Nd:YAG laser (Quantel, Paris, France) driving 5-ns pulses. The frequency, delivery energy, and wavelength of the pulsed laser were 20 Hz, 16 mJ, and 266 nm (Nd-YAG), respectively. In this system, in the spectral range of 200–1000 nm, an intensified charge-coupled device camera (iStar, Andor Technology, Ltd., Belfast, Northern Ireland) was used to collect the diffracted light. We set 2 × 2 matrices for each shot.
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