Quasi-BIC sensor demonstrates high sensitivity in detecting organic compounds, indicating strong potential for on-chip applications.
Bound states in the continuum (BICs) can be transformed into quasi-bound states (quasi-BICs) via intentional symmetry breaking, thereby enabling ultrahigh-Q resonances critical for refractometric sensing applications. To advance detection capabilities for organic analytes, we proposed an all-dielectric metasurface monolithically integrated within a microfluidic channel. Mirror symmetry was intentionally disrupted through a cylindrical perturbation applied to one of two identical elliptical resonators, which excited a quasi-BIC mode at 1.9591 THz with a numerically validated Q-factor of 1959. This resonance manifested an absorption peak approaching unity, featuring a full-width at half-maximum (FWHM) of merely 1 GHz. Multipolar decomposition revealed that the mode originated from a synergistic electric-quadrupole (EQ)–magnetic-dipole (MD) pair, wherein the EQ contribution exceeded the MD counterpart by 20%. Capitalizing on this high-Q resonance, the sensor attained a sensitivity of 240 GHz per refractive-index unit (GHz RIU−1) and a figure of merit (FOM = S/FWHM) of 240, while demonstrating robust performance against fabrication tolerances spanning −4% to +4%. Additionally, we verified that oblique-incidence illumination could activate a quasi-BIC within the identical spectral band, circumventing the need for structural asymmetry and thus expanding operational versatility. Benefiting from its geometric simplicity and competitive performance, this architecture exhibited substantial potential for on-chip sensing of organic compounds.
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Wang et al. (2026) studied this question.
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