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| Main Authors: | , |
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| Format: | Preprint |
| Published: |
2026
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| Subjects: | |
| Online Access: | https://arxiv.org/abs/2601.17889 |
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Table of Contents:
- Terahertz (THz) spectroscopy holds transformative potential for non-invasive sensing, yet characterizing individual nanoparticles in complex biological environments remains challenging due to the far-field diffraction limit. While near-field dipolar theory is well established, its application to characterizing/identifying nanoparticles immersed in complex media at THz frequencies is largely unexplored. This work utilizes numerical simulations of magneto-optical (MO) heterodimers -- comprising n-doped Indium Antimonide (n-InSb) and isotropic or birefringent particles (e.g., SiO2, GaSe) -- under counter-propagating, circularly polarized THz illumination. We demonstrate that while far-field observables like absorption cross-sections are often dominated by the MO-active particle, mechanical variables-specifically induced binding forces and spin/orbital torques-exhibit superior sensitivity for detecting "hidden" neighboring components. Because these mechanical signatures depend directly on near-field interactions, they provide higher information density regarding interparticle coupling. Key findings reveal material-specific spectral "hotspots" and "zeros" that serve as robust calibration markers even within dispersive biological surrogates. We show that the spin torque on non-MO particles is significantly modified by MO-neighbor proximity, a phenomenon controllable via static magnetic fields. Furthermore, these variables exhibit high angular sensitivity in perpendicular configurations. Our results provide a roadmap for using optomechanical signatures as high-resolution detectors for in-vivo diagnostics, signal transduction, and low-energy nanocircuit control.