Photon Counting Detectors

Complete confocal fluorescence microscope that empowers researchers to advance quantitative functional imaging from individual molecules to cells and tissues.

Modular, customizable, time-resolved confocal microscope with single-molecule sensitivity for life and materials science.

Compact FLIM and FCS upgrade kit that adds advanced functional imaging and correlation analysis to existing laser scanning microscopes.

Designed for flexible, sensitive, and precise steady-state and time-resolved spectroscopy across the UV to NIR range and time scales from picoseconds to milliseconds.

Modular lifetime spectrometer designed for flexible fluorescence and photoluminescence measurements in both materials and life science research.

Add spectral and time-resolved photoluminescence to your setup through flexible microscope–spectrometer coupling options.

Get the most out of superconducting nanowire detectors in large-scale quantum communication and computing experiments requiring precise multichannel timing.

Boost your time-resolved experiments with a flexible, high-precision time tagging and TCSPC unit for materials science and quantum sensing.

Scale your photonic quantum computing and detector characterization setups while maintaining performance, flexibility, and high data throughput.

Compact 3-color picosecond laser delivering flexible ns to ms excitation with cost-effective multicolor performance and straightforward operation.

Smart picosecond laser diode heads covering UV-A to NIR, providing the right combination of power, pulse width, and diode type for any time-resolved technique.

VisUV provides clean short pulses and stable timing across key UV and visible wavelengths, including deep UV lines as well as 488 nm and 532 nm.

Enhance your single-photon counting experiments with wide dynamic range and excellent timing precision in the UV and visible even at the highest count rates.

Capture even the weakest signals over large areas with maximum dynamic range and enhanced low-light sensitivity in a compact detector design.

Unlock spatially resolved single-photon detection with a 23-pixel SPAD array, combining low dark counts and precise time tagging for advanced experiments.

Advanced FLIM analysis software for fast, accurate interpretation of lifetime imaging data.

Intuitive, free software solution for real-time, high-precision photon data acquisition, visualization, and initial data analysis.

Advanced software for time-resolved fluorescence acquisition and analysis.

An imaging technique that uses fluorescence lifetimes to generate image contrast.

Investigating how proteins dynamically explore multiple conformational states that control biological function.

Investigating how biomolecules separate into dynamic liquid phases to organize cellular space and regulate biological function.

A time-resolved technique that measures photoluminescence lifetimes to reveal excited-state dynamics in materials.

Studying exciton dynamics, charge carrier processes, and structural properties through optical and time-resolved characterization methods.

Investigating charge-carrier lifetimes and recombination dynamics to enable precise optical characterization of material quality and device performance.

A quantum optical signature revealed by time-resolved photon correlation analysis to identify single-photon emission in materials and nanostructures.

The transmission of information using individual photons, using quantum effects to ensure absolute security.

Quantifying photons per detection event enables direct access to photon-number statistics, providing insight into quantum and statistical properties of light.

An optical technique that analyzes light emission under electrical excitation to reveal electronic properties of electroluminescent materials.

Monitoring environmental signals and trace compounds to understand dynamic changes in natural and engineered environments.

A photon timing technique that measures single-photon arrival times to resolve ultrafast dynamics in fluorescence, materials research, and quantum optics.
Two-dimensional materials represent a distinct class of solids in which electrons and excitations are confined to atomically thin layers. This reduced dimensionality leads to physical behavior that differs fundamentally from bulk materials. Research in this field focuses on understanding how atomic thickness, crystal symmetry, and environmental interactions shape optical and electronic properties of these systems.
The optical response of atomically thin materials is governed by strong Coulomb interactions, reduced dielectric screening, and modified electronic band structures. As a result, light absorption and emission processes are highly sensitive to layer number, substrate effects, and local environment. Photoluminescence and absorption spectroscopy reveal information about band gaps, excitonic resonances, and radiative efficiency, offering direct insight into the electronic structure of two-dimensional systems.
Excitons dominate the optical behavior of many two-dimensional materials due to their large binding energies and long interaction times. Following optical excitation, charge carriers undergo relaxation, scattering, and recombination on timescales ranging from femtoseconds to nanoseconds. Resolving these ultrafast dynamics is essential for understanding energy dissipation, nonradiative pathways, and the influence of defects or interfaces on carrier lifetimes.
The atomic-scale structure strongly influences the optical response of two-dimensional materials. Variations in crystal orientation, grain boundaries, strain, and layer stacking introduce spatial heterogeneity that affects emission energy and dynamics. Defects can act as recombination centers or localized quantum emitters, while interlayer coupling modifies electronic states in multilayer systems. Mapping these effects requires advanced methods capable of correlating local structural order with optical response at the nanoscale.
Optical spectroscopy and time-resolved techniques provide direct access to the processes governing light emission and carrier dynamics in two-dimensional materials. Time-resolved photoluminescence (TRPL) reveals recombination pathways and lifetimes, while spectrally and spatially resolved approaches capture heterogeneity across flakes and devices. Nonlinear optical methods add sensitivity to symmetry and layer structure, enabling comprehensive characterization across multiple length and time scales.
Transition metal disulfides and dichalcogenides are prototypical two-dimensional semiconductors with strong light–matter interaction. Their optical response is governed by excitonic effects, structural defects, and local atomic order, making them ideal model systems for studying charge carrier dynamics recombination mechanisms, and exciton behavior in low-dimensional materials.

Monolayer MoS₂ and WSe₂ on flexible substrates were investigated using reflection imaging, SHG, TRPL, and two-photon excitation TRPL. Combining linear and nonlinear optical contrasts within a single microscope enables local correlation of structure, symmetry, and emission dynamics in two-dimensional dichalcogenide monolayers.

Confocal TRPL measurements on chemically treated monolayer MoS₂ reveal how different treatments modify radiative recombination and exciton transport. Changes in decay dynamics and spatial PL profiles indicate treatment-dependent recombination rates and exciton diffusion, providing insight into mechanisms governing photoluminescence enhancement in TMDs.
Webinar on quantum optics in 2D TMD materials featuring multimodal imaging with MicroTime 100 and FluoTime 300 to study photoluminescence and light–matter interactions.
Second-harmonic generation imaging with picosecond lasers reveals crystal structure, defects, and layer orientation in advanced materials.
How time-resolved fluorescence spectroscopy and microscopy reveal excited-state dynamics, defects, and charge-carrier processes
Poster on high-spatial photoluminescence studies of nanostructures and quantum emitters using time-resolved confocal microscopy and spectroscopy.
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