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Idus 420

Manufactured by Oxford Instruments
Sourced in Ireland

The IDus 420 is a high-performance, back-illuminated CCD detector designed for spectroscopic applications. It features a large active area, low noise, and high quantum efficiency across a wide spectral range.

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5 protocols using idus 420

1

Near-Infrared Spectroscopy Imaging of Mouse Cortex

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The NIRS system included a broadband white light source (77501, Oriel Instruments Inc., USA), two 5 m long Hard-Clad Silica Core Multimode optical fibres (FT1000EMT, Thorlabs Inc, USA) with a 1000 µm core diameter and 0.39 NA, a spectrograph (Shamrock 303i, Andor Technology Inc, Northern Ireland), and a CCD camera (iDus 420, Andor Technology Inc, Northern Ireland). A GRIN lens with a 1.80 mm diameter and 0.55 NA (#64-525, Edmund Optics, USA) and a 90° prism with a leg length of 2 mm (#45-524, TECHSPEC NSF11, Edmund Optics, USA) were glued to the end of the fibers to collimate the light and direct it from the source fibre into the tissue and from the tissue into the detector fibre. Attenuation spectra were collected from the mouse cortex over the range 705–960 nm.
Hair was removed from the animal head, and the fibers, with a thin layer of glycerol19
on the prisms, were secured on top of the head, near bregma, with the posterior edge of the prisms placed on the line between the two external auditory meatus (within 1 mm of the interaural line). Fibers were spaced with a black rubber separator (4 mm width) and secured by covering the area with masking tape connected to the outside of the MRI coil cradle.
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2

Raman Spectra Acquisition for Indene

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Raman spectra were excited with 514.5 nm light from an Ar+ ion laser (Innova 200, Coherent, 500 mW). Scattered light was collected by a f/1.2 camera lens (Nikon) in a 45° backscattering geometry and analyzed by triple spectrometer (Triplemate 1877, Spex) equipped with CCD camera (iDUS 420, Andor). The spectral resolution at the excitation wavelength was 0.2 nm. Raman spectrum of indene was used for the spectral calibration.
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3

Time-Resolved Photoluminescence Spectroscopy

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Time‐resolved PL spectroscopy and imaging measurements were performed by a home‐build system, which mainly includes fs pulsed laser, an inverted fluorescence microscope, and a spectrometer integrated with Time‐Correlated Single Photon Counting (TCSPC) detection. The excitation laser pulses were generated from a wavelength‐tunable femtosecond oscillator (Coherent Chameleon) with 200 fs pulse width and a repetition rate of 80 MHz. The excitation laser was introduced into the microscopy (Olympus IX71) and focused on the sample via an objective lens (60×). The optical image was taken by two Scientific CMOS cameras (PCO.panda 4.2 & Sony Starvis IMX226). Short‐pass filters (for two‐photon excitation) or long‐pass filters (for one‐photon excitation) were placed in the detection path to cut off the excitation laser before measuring. The sample was placed on a 3D nano‐translation stage (Physik Instrumente, P‐525) for varying the sample position precisely. The collected emission was further imported into a spectrometer (Andor Kymera‐328i) with two output ports. One port was connected with a charge‐coupled device (CCD) camera (Andor iDus420) for the spectra measurement. The other one was integrated with a photomultiplier detector (PicoQuant PMA182) which was associated with TCSPC (HydraHarp 400) for transient PL measurement.
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4

Fluorescence Quantum Yield Measurement

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The fluorescence quantum yields were measured and determined according to the procedure described in47 (link). The measurements on SCP were carried out at room temperature using a laser diode (Thorlabs, HL6358MG) operating at 639 nm as excitation light source. For detection a CCD-camera (ANDOR IDUS 420) that was connected to a spectrograph (MS125), which in turn was fibre-coupled to an integrating sphere was used.
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5

Photoluminescence Spectroscopy of Nanogap Samples

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The prepared TMD MLs on the nanogap were loaded onto a piezoelectric transducer (PZT, P-611.3X, Physik Instrumente) for XY scanning. To obtain a high-quality wavefront of the excitation beam, a He–Ne laser (594.5 nm, <1.0 mW) was coupled and passed through a single-mode fiber (core diameter of ~3.5 μm) and collimated again using an aspheric lens. Finally, the beam was focused onto the sample using a microscope objective (NA = 0.8, LMPLFLN100X, Olympus). The PL responses were collected using the same microscope objective (backscattering geometry) and passed through an edge filter (FEL0550, Thorlabs) to remove the fundamental laser line. The PL signals were then dispersed onto a spectrometer (f = 328 mm, Kymera 328i, Andor) and imaged using a thermoelectrically cooled charge-coupled device (CCD, iDus 420, Andor) to acquire the PL spectra. Before the experiment, the spectrometer was calibrated using a mercury–argon lamp. A 150 g/mm grating blazed to 800 nm (spectral resolution of 0.62 nm) was used for PL measurements. Time-resolved PL measurements were performed with a time-correlated single-photon counting (TCSPC) method. A commercially available TCSPC module (PicoHarp, PicoQuant GmbH) was used to obtain the PL decay curves. A 405 nm picosecond laser diode with an 80 MHz repetition rate was used as an excitation source.
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