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This lifetime was measured on a FLIM system that had an excitation laser pulse width of less than 200 fs, and was acquired using a microchannel plate photomultiplier tube (Hammamatsu R3809U-52) thad had a measured system response function of <40 ps (FWHM; Fig. 1A).
The TEY yield was recorded using a microchannel plate detector.
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Using a microchannel-plate detector with time of flight resolution and x-y-position resolution for detection of the recoiling metastable excited atoms, we obtain 4π-acceptance for electron scattering.
The scintillation light is collected at each end of the pillar using a photodetector, e.g., a microchannel plate photomultiplier (MCP-PM) or a silicon photomultiplier (SiPM).
The detector technology typically used for protein imaging, a microchannel plate, is not well suited to the detection of high m/z ions and is prone to detector saturation when analyzing complex mixtures.
We describe novel electronics for processing signals from a microchannel plate detector using a resistive anode readout.
A set of ion optics consisting of a repeller, an extractor and a grounded plate is used to accelerate the ions towards a microchannel plate detector (MCP) connected to a phosphor screen.
Here, a microchannel plate is used to amplify electrons being backscattered by the sample.
A microchannel plate photomultiplier tube (MCP-PMT, Hamamatsu R3809U-50) was used to detect the fluorescence photons.
Area detection of the fluorescence intensity was acquired in reflection mode using a 780 nm fluorescence filter and standard 50 mm lens (Nikon) mounted to a microchannel plate (Picostar HRI, La Vision) for signal amplification, which was coupled to an electron-multiplying CCD camera (Andor) to capture the image.
The ejected electrons are focused using a unipolar electrostatic lens and conical electrostatic mirror to form a magnified image on a microchannel plate (MCP).
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