Harnessing coherent-wave control for sensing applications

TL;DR

This paper develops a microscopic theory for optical sensitivity in wavefront-shaped imaging, enabling enhanced deep tissue sensing by leveraging interference effects beyond traditional diffusion models.

Contribution

It introduces a microscopic approach to optical sensitivity, compares wavefront shaping strategies, and demonstrates methods for global sensitivity enhancement compatible with existing imaging algorithms.

Findings

Microscopic theory captures interference effects neglected by diffusion models.

Phase conjugation yields maximum local sensitivity enhancement.

Remission eigenchannel provides a global sensitivity boost with fixed wavefront.

Abstract

Imaging techniques such as functional near-infrared spectroscopy (fNIRS) and diffuse optical tomography (DOT) achieve deep, non-invasive sensing in turbid media, but they are constrained by the photon budget. Wavefront shaping (WFS) can enhance signal strength via interference at specific locations within scattering media, enhancing light-matter interactions and potentially extending the penetration depth of these techniques. Interpreting the resulting measurements rests on the knowledge of optical sensitivity - a relationship between detected signal changes and perturbations at a specific location inside the medium. However, conventional diffusion-based sensitivity models rely on assumptions that become invalid under coherent illumination. In this work, we develop a microscopic theory for optical sensitivity that captures the inherent interference effects that diffusion theory necessarily neglects. We analytically show that under random illumination, the microscopic and diffusive treatments coincide. Using our microscopic approach, we explore WFS strategies for enhancing optical sensitivity beyond the diffusive result. We demonstrate that the input state obtained through phase conjugation at a given point inside the system leads to the largest enhancement of optical sensitivity but requires an input wavefront that depends on the target position. In sharp contrast, the maximum remission eigenchannel leads to a global enhancement of the sensitivity map with a fixed input wavefront. This global enhancement equals to remission enhancement and preserves the spatial distribution of the sensitivity, making it compatible with existing DOT reconstruction algorithms. Our results establish the theoretical foundation for integrating wavefront control with diffuse optical imaging, enabling deeper tissue penetration through improved signal strength in biomedical applications.