No abstract

Thick biological tissues give rise to not only the multiple scattering of incoming light waves, but also the aberrations of remaining signal waves. The challenge for existing optical microscopy methods to overcome both problems simultaneously has limited sub-micron spatial resolution imaging to shallow depths. Here we present an optical coherence imaging method that can identify aberrations of waves incident to and reflected from the samples separately, and eliminate such aberrations even in the presence of multiple light scattering. The proposed method records the time-gated complex-field maps of backscattered waves over various illumination channels, and performs a closed-loop optimization of signal waves for both forward and phase-conjugation processes. We demonstrated the enhancement of the Strehl ratio by more than 500 times, an order of magnitude or more improvement over conventional adaptive optics, and achieved a spatial resolution of 600 nm up to an imaging depth of seven scattering mean free paths.

The efficient delivery of light energy is a prerequisite for non-invasive imaging and stimulating of target objects embedded deep within a scattering medium. However, injected waves experience random diffusion by multiple light scattering, and only a small fraction reaches the target object. Here we present a method to counteract wave diffusion and to focus multiplescattered waves to the deeply embedded target. To realize this, we experimentally inject light to the reflection eigenchannels of a specific flight time where most of the multiple-scattered waves have interacted with the target object and maximize the intensity of the returning multiple-scattered waves at the selected time. For targets that are too deep to be visible by optical imaging, we demonstrated a more than 10-fold enhancement in light energy delivery in comparison with ordinary wave diffusion cases. This work will lay a foundation for enhancing the working depth of imaging, sensing, and light stimulation.