Theory of self-induced back-action optical trapping in nanophotonic systems

Optical trapping is an indispensable tool in physics and the life sciences. However, there is a clear trade off between the size of a particle to be trapped, its spatial confinement, and the intensities required. This is due to the decrease in optical response of smaller particles and the diffraction limit that governs the spatial variation of optical fields. It is thus highly desirable to find techniques that surpass these bounds. Recently, a number of experiments using nanophotonic cavities have observed a qualitatively different trapping mechanism described as "self-induced back-action trapping" (SIBA). In these systems, the particle motion couples to the resonance frequency of the cavity, which results in a strong interplay between the intra-cavity field intensity and the forces exerted. Here, we provide a theoretical description that for the first time captures the remarkable range of consequences. In particular, we show that SIBA can be exploited to yield dynamic reshaping of trap potentials, strongly sub-wavelength trap features, and significant reduction of intensities seen by the particle, which should have important implications for future trapping technologiesComment: 7 pages, 5 figure

Strong Optomechanical Coupling at Room Temperature by Coherent Scattering

Quantum control of a system requires the manipulation of quantum states faster than any decoherence rate. For mesoscopic systems, this has so far only been reached by few cryogenic systems. An important milestone towards quantum control is the so-called strong coupling regime, which in cavity optomechanics corresponds to an optomechanical coupling strength larger than cavity decay rate and mechanical damping. Here, we demonstrate the strong coupling regime at room temperature between a levitated silica particle and a high finesse optical cavity. Normal mode splitting is achieved by employing coherent scattering, instead of directly driving the cavity. The coupling strength achieved here approaches three times the cavity linewidth, crossing deep into the strong coupling regime. Entering the strong coupling regime is an essential step towards quantum control with mesoscopic objects at room temperature

On-a-chip biosensing based on all-dielectric nanoresonators

Nanophotonics has become a key enabling technology in biomedicine with great promises in early diagnosis and less invasive therapies. In this context, the unique capability of plasmonic noble metal nanoparticles to concentrate light on the nanometer scale has widely contributed to biosensing and enhanced spectroscopy. Recently, high-refractive index dielectric nanostructures featuring low loss resonances have been proposed as a promising alternative to nanoplasmonics, potentially offering better sensing performances along with full compatibility with the microelectronics industry. In this letter we report the first demonstration of biosensing with silicon nanoresonators integrated in state-of-the-art microfluidics. Our lab-on-a-chip platform enables detecting Prostate Specific Antigen (PSA) cancer marker in human serum with a sensitivity that meets clinical needs. These performances are directly compared with its plasmonic counterpart based on gold nanorods. Our work opens new opportunities in the development of future point-of-care devices towards a more personalized healthcare

Unravelling the Role of Electric and Magnetic Dipoles in Biosensing with Si Nanoresonators

High refractive index dielectric nanoresonators are attracting much attention due to their ability to control both electric and magnetic components of light. Combining confined modes with reduced absorption losses, they have recently been proposed as an alternative to nanoplasmonic biosensors. In this context, we study the use of semi-random silicon nanocylinder arrays, fabricated with simple and scalable colloidal lithography for the efficient and reliable detection of biomolecules in biological samples. Interestingly, electric and magnetic dipole resonances are associated to two different transduction mechanisms: extinction decrease and resonance redshift, respectively. By contrasting both observables, we identify clear advantages in tracking changes in the extinction magnitude. Our data demonstrate that, despite its simplicity, the proposed platform is able to detect prostate specific antigen (PSA) in human serum with limits of detection meeting clinical needs.Peer ReviewedPostprint (author's final draft