Fluorescence lifetime imaging via spatio-temporal speckle patterns in a single-pixel camera configuration

Photoluminescence (PL) spectroscopy offers excellent methods for mapping the PL decay on the nanosecond time scale. However, capturing maps of emission dynamics on the microsecond timescale can be highly time-consuming. We present a new approach to fluorescence lifetime imaging (FLIM), which combines the concept of random temporal speckles excitation (RATS) with the concept of a single-pixel camera based on spatial speckles. The spatio-temporal speckle pattern makes it possible to map PL dynamics with unmatched simplicity. Moreover, the method can acquire all the data necessary to map PL decay on the microsecond timescale within minutes. We present proof-of-principle measurements for two samples and compare the reconstructed decays to the non-imaging measurements. Finally, we discuss the effect of the preprocessing routine and other factors on the reconstruction noise level. The presented method is suitable for lifetime imaging processes in several samples, including monitoring charge carrier dynamics in perovskites or monitoring solid-state luminophores with a long lifetime of PL. (c) 2021 Optical Society of America under the terms of the OSA Open Access Publishing Agreement

Automated summary

The new fluorescence lifetime imaging method combines the concept of random temporal speckles excitation with a single-pixel camera, enabling the mapping of PL dynamics on the microsecond timescale within minutes. It is a simple and efficient approach for monitoring charge carrier dynamics and solid-state luminophores.