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Spcm aqrh 16

Manufactured by Excelitas

The SPCM-AQRH-16 is a single-photon counting module designed for low-light applications. It features a high-efficiency, low-noise silicon avalanche photodiode detector. The module provides a digital output pulse for each detected photon, with a high timing resolution.

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3 protocols using spcm aqrh 16

1

Confocal Microscopy for Exciton Dynamics

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A confocal microscope is used to optically excite IXs and collect the emitted photons through the same objective with a working distance 4.5 mm and NA = 0.65. IXs are excited using sub-ps pulses with a repetition rate of 80 MHz from Ti:Sapphire laser. The collected photons are sent to a APD (Excelitas Technologies, SPCM-AQRH-16) mounted on a 2D motorized translational stage. The output of the APD is connected to a time-correlated photon counting module (TCPCM) with a resolution of 12 ps r.m.s. (PicoQuant, PicoHarp 300), which measures the arrival time of each photon. For the measurements in this work, we set the time bin to 64 ps to record the photon clicks. The single-photon timing resolution of the APD is ~ 350 ps, which is the main time-limitation for the setup. Technical details can be found in Supplementary Note 3.
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2

Cryogenic Confocal Microscopy of Fluorescent Samples

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The samples were measured in a liquid helium flow cryostat (Janis, SVT‐200‐5) that can reach a working temperature of 1.3 K. With an objective (0.85 NA, Edmund Optics) immersed in liquid helium, the cryostat forms part of a home‐built confocal microscope. A Ti:sapphire laser (M‐squared SolsTiS) in combination with a frequency‐doubling module (M‐squared ECD‐X) was used as a narrow bandwidth (<1 MHz) tunable excitation source, operating in the 440–460 nm range. The output wavelength of the laser was measured continuously with a wavemeter (High Finesse WS6‐200), with resolution of a few MHz. A dichroic mirror (Semrock, FF458‐Di02‐25x36) was used to separate fluorescence from the excitation light and further filtering was done by a long‐pass filter (Chroma, ET460lp). The laser beam was scanned over the sample by a scanning mirror (Newport, FSM‐300‐01) and fluorescence was detected by an avalanche photodiode (Excelitas, SPCM‐AQRH‐16). Fluorescence spectra were recorded with a Horiba iHR320 spectrometer coupled to a liquid‐nitrogen‐cooled Symphony II CCD detector. The excitation intensity was measured with a power meter (Newport 1830‐C), before the laser beam entered the cryostat.
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3

Confocal Microscopy for Exciton Dynamics

Check if the same lab product or an alternative is used in the 5 most similar protocols
A confocal microscope is used to optically excite IXs and collect the emitted photons through the same objective with a working distance 4.5 mm and NA = 0.65. IXs are excited using sub-ps pulses with a repetition rate of 80 MHz from Ti:Sapphire laser. The collected photons are sent to a APD (Excelitas Technologies, SPCM-AQRH-16) mounted on a 2D motorized translational stage. The output of the APD is connected to a time-correlated photon counting module (TCPCM) with a resolution of 12 ps r.m.s. (PicoQuant, PicoHarp 300), which measures the arrival time of each photon. For the measurements in this work, we set the time bin to 64 ps to record the photon clicks. The single-photon timing resolution of the APD is ~ 350 ps, which is the main time-limitation for the setup. Technical details can be found in Supplementary Note 3.
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