Applications:
FLIM
(fluorescence-lifetime imaging microscopy)
The decay time of an excited fluorophore is typically in the range of a few nanoseconds. In fluorescence lifetime imaging the exponential decay of a sample is determined requiring a timing resolution in the picosecond regime.
LIDAR
also known as: LIDAR, LiDAR, and LADAR, "light detection and ranging", "laser imaging, detection, and ranging", "3-D laser scanning", "LIDAR mapping", "airborne laser scanning", ALS
LIDAR Systems emit ultraviolet, visible, or near-infrared light to image objects and measuring the time-of-flight (TOF) of reflected photons. Such systems are used for object detection and tracking in many different fields, ranging from archaeology to agriculture, autonomous vehicles and robots etc.
OTDR
optical time-domain reflectometry, optical time-domain reflectometer, remote fiber testing
In optical time-domain reflectometry the time of the reflections is determined from the reflection loss by measuring from the same end of the fiber how much light returns via the Rayleigh backscatter or is being reflected from individual locations along the fiber.
TOF mass spectrometry
TOF- & MASS- spectroscopy detectors, TOFMS
In many TOFMS units cronologic TDCs are used to measure precisely the arrival of single ions. From the arrival time, the ion’s time-of-flight is deduced, from which the mass-to-charge ratio of the detected particle can be determined.
Time Domain Reflectometry
TDR, distance-to-fault, DTF
TDR (Time Domain Reflectometry) is an electronic measurement method that measures reflections along a conductor. It belongs to the category of Distance-to-Fault (DTF) measurements. TDR measurements provide meaningful information about the broadband behavior of transmission systems.
fluorescence lifetime correlation spectroscopy
FLCS, FCS, fluorescence lifetime correlation spectroscopy
Fluorescence-correlation-spectroscopy is a highly sensitive optical measurement method. Fluctuations in the fluorescence emission intensity over time are recorded, which are caused by individual fluorophores that pass through the detection volume.
