Broadly tunable quantum-enhanced Raman microscopy for advancing bioimaging

arXiv:2511.01430 · physics.optics, quant-ph · Submitted 2025-11-03 · Read on arXiv

physics.optics, quant-ph

Submitted: 2025-11-03

Updated: 2026-03-10

Comments: 13 pages, 7 figures

DOI: 10.1364/OPTICAQ.583523

License: http://creativecommons.org/licenses/by-nc-nd/4.0/

The gist: Stimulated Raman scattering (SRS) microscopy has emerged as a powerful technique for probing the spatiotemporal dynamics of molecular bonds with exceptional sensitivity, resolution, and speed.

Terminology

Abstract

Stimulated Raman scattering (SRS) microscopy has emerged as a powerful technique for probing the spatiotemporal dynamics of molecular bonds with exceptional sensitivity, resolution, and speed. However, classically, its performance remains fundamentally constrained by optical shot noise, which imposes a strict limit on detection sensitivity and speed. Here, we demonstrate a quantum-enhanced SRS microscopy platform that circumvents this barrier by harnessing amplitude-squeezed light. Specifically, we generate a Stokes beam with 5.2 dB of amplitude squeezing using traveling-wave optical parametric amplification in second-order nonlinear waveguides, and combine it with a tunable coherent pump to access vibrational modes spanning from 1000 to 3100 cm-1. Applied to quantum imaging of metabolites in biological tissue (pork muscle), our quantum-enhanced Raman microscope achieves an average noise suppression of 3.6 dB and a 51% enhancement in signal-to-noise ratio (SNR) -- to the best of our knowledge, the largest improvement reported to date in quantum-enhanced SRS microscopy of biological samples.

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