In practical applications such as cancer diagnosis and industrial detection, there is a critical demand for fast fluorescence lifetime imaging (Fast-FLIM). The Fast-FLIM systems suitable for complex environments are typically achieved by enhancing the hardware performance of time-correlated single-photon counting (TCSPC), with an acquisition speed of about a few frames per second (fps). However, due to the limitation of single-photon acquisition, the imaging speed is still far from the demand of practical application. The synchroscan streak camera (SC) maps signals from the temporal dimension to the spatial dimension, effectively overcoming the long acquisition time caused by single-photon acquisition. This paper constructs a method to calculate the acquisition time for the TCSPC-FLIM and SC-FLIM systems, and it quantitatively compares the speed. The research demonstrates that the main factors limiting the acquisition speed of the FLIM systems are the photon emission rate, the photon counting rate, the required SNR, the dwell time, and the number of parallel channels. In high-quality and large-scale lifetime imaging, the acquisition speed of the SC-FLIM is at least 104 times faster than that of the TCSPC-FLIM. Therefore, the synchroscan streak camera has more significant potential to promote Fast-FLIM.
