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Confocal microscopy
SPAD arrays increase light collection and enable innovation in the field of confocal scanning microscopy. This innovation finally leads to a sharper and brighter image with functional information about the underlying molecular function, interactions and environment.
Why SPAD arrays?
Achieve super-resolution with a standard confocal microscope
Increase light collection
Increase imaging speed
Reduce background noise
Applications
Image scanning microscopy (ISM)
Quantum ISM (Q-ISM)
Super-resolution optical fluctuation ISM (SOFI-ISM)
Fluorescence lifetime imaging (FLIM)
Foerster resonance energy transfer (FRET)
Fluorescence correlation spectroscopy (FCS)
Stimulated emission depletion microscopy (STED)
Quantum information
Temporal photon correlations and photon number resolving (PNR) are fundamental to probing the quantum properties of light. Our detector has an extremely low crosstalk and thus enables reliable measurements of second and third order photon correlations, as well as quantum random number generation for unbreakable encryption.
Why SPAD arrays?
Simplify setup with single-chip multi-channel detector
Increase data rate with detector parallelization
Photon number resolving (PNR) detection
Applications
Antibunching
Coincidence correlation
Quantum random number generation
Widefield fluorescence lifetime imaging
SPAD cameras increase the overall photon throughput compared to scanned detection systems from the typical 10 Mcounts per second to 26 Gcounts per second.
Why SPAD cameras?
Simplify FLIM setup
Increase FLIM frame rate
High-speed imaging
SPAD cameras enable high frame rates with global shutter at no readout noise cost.