Bright Pulsed Squeezed Light for Quantum-Enhanced Precision Microscopy
Alex Terrasson, Lars Madsen, Joel Grim, Warwick Bowen
TL;DR
This work tackles the need for bright, pulsed squeezed light to surpass the standard quantum limit in nonlinear microscopy. It introduces a compact, single-pass $χ^2$ OPA in a PPLN waveguide with LO co-propagation and post-OPA displacement to produce bright amplitude squeezing suitable for picosecond pulses at biologically compatible powers. Key results include direct-detection squeezing of $-3.2$ dB and homodyne squeezing of $-3.6$ dB (vacuum case $-3.6$ dB), with loss-corrected waveguide squeezing of $-15.4^{+2.7}_{-8.7}$ dB, and near-ideal spatial/temporal mode overlaps ($0.997$ and $0.977$). The work projects substantial gains for quantum-enhanced nonlinear microscopy, estimating up to $-6.2$ dB bright squeezing under practical detector efficiencies, enabling device-independent quantum advantages in SRS and related imaging modalities.
Abstract
Squeezed states of light enable enhanced measurement precision by reducing noise below the standard quantum limit. A key application of squeezed light is nonlinear microscopy, where state-of-the-art performance is limited by photodamage and quantum-limited noise. Such microscopes require bright, pulsed light for optimal operation, yet generating and detecting bright pulsed squeezing at high levels remains challenging. In this work, we present an efficient technique to generate high levels of bright picosecond pulsed squeezed light using a $χ^2$ optical parametric amplification process in a waveguide. We measure $-3.2~\mathrm{dB}$ of bright squeezing with optical power compatible with nonlinear microscopy, as well as $-3.6~\mathrm{dB}$ of vacuum squeezing. Corrected for losses, these squeezing levels correspond to $-15.4^{+2.7}_{-8.7}~\mathrm{dB}$ of squeezing generated in the waveguide. The measured level of bright amplitude pulsed squeezing is to our knowledge the highest reported to date, and will contribute to the broader adoption of quantum-enhanced nonlinear microscopy in biological studies.
