English

Efficient wide-field FLIM

Optics 2021-03-09 v2 Biological Physics Instrumentation and Detectors

Abstract

Nanosecond temporal resolution enables new methods for wide-field imaging like time-of-flight, gated detection, and fluorescence lifetime. The optical efficiency of existing approaches, however, presents challenges for low-light applications common to fluorescence microscopy and single-molecule imaging. We demonstrate the use of Pockels cells for wide-field image gating with nanosecond temporal resolution and high photon collection efficiency. Two temporal frames are obtained by combining a Pockels cell with a pair of polarizing beam-splitters. We show multi-label fluorescence lifetime imaging microscopy (FLIM), single-molecule lifetime spectroscopy, and fast single-frame FLIM at the camera frame rate with 10310510^3 - 10^5 times higher throughput than single photon counting. Finally, we demonstrate a space-to-time image multiplexer using a re-imaging optical cavity with a tilted mirror to extend the Pockels cell technique to multiple temporal frames. These methods enable nanosecond imaging with standard optical systems and sensors, opening a new temporal dimension for low-light microscopy.

Keywords

Cite

@article{arxiv.1812.06563,
  title  = {Efficient wide-field FLIM},
  author = {Adam J. Bowman and Brannon B. Klopfer and Thomas Juffmann and Mark A. Kasevich},
  journal= {arXiv preprint arXiv:1812.06563},
  year   = {2021}
}

Comments

11 pages, 6 figures

R2 v1 2026-06-23T06:44:03.314Z