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In the last years, single-pixel imaging (SPI) has been extensively utilized in fluorescence lifetime imaging (FLIM) experiments. In this context, to attain high temporal resolution, time-correlated single photon counting (TCSPC) is typically adopted, with the major drawback of the pile-up phenomenon, that limits the photon count rate to 1-5% of the laser excitation rate. This clearly hinders the possibility of monitoring a wide variety of biological phenomena in real-time. In this paper, to the best of our knowledge, we apply for the first time to a single-pixel camera (SPC) a hardware-based method, that allows to completely avoid the onset of pile-up by matching the dead time of the employed single-photon avalanche diode (SPAD) detector to an integer multiple of the laser period. We therefore demonstrate that undistorted and high-fidelity lifetime maps can be acquired at count rates (40%) well above the classic pile-up limitation, even in the presence of computational imaging algorithms. These results are supported by a thorough analysis of both the raw data prior to the reconstruction process and the final reconstructed lifetime maps.
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Farina et al. (2025) studied this question.
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