Photon-efficient optical tweezers via wavefront shaping.

Optical tweezers enable noncontact trapping of microscale objects using light. It is not known how tightly it is possible to three-dimensionally (3D) trap microparticles with a given photon budget. Reaching this elusive limit would enable maximally stiff particle trapping for precision measurements on the nanoscale and photon-efficient tweezing of light-sensitive objects. Here, we customize the shape of light fields to suit specific particles, with the aim of optimizing trapping stiffness in 3D. We show, theoretically, that the confinement volume of microspheres held in sculpted optical traps can be reduced by one to two orders of magnitude. Experimentally, we use a wavefront shaping-inspired strategy to passively suppress the Brownian fluctuations of microspheres in every direction concurrently, demonstrating order-of-magnitude reductions in their confinement volumes. Our work paves the way toward the fundamental limits of optical control over the mesoscopic realm.

Infrared plasmonic meta-modes via near-field coupling of metallic nanorods with split-ring resonators.

We study the anomalous optical properties of lattices formed via periodic arrangement of a plasmonic unit structure consisting of a metallic nanorod and U-shape split-ring resonator. When the units are closely packed, i.e., small lattice constants, and the incident light is polarized along the transverse axis of the nanorods, our results show that the near-field plasmonic coupling of these units leads to a lattice-induced meta-mode. Such a meta-mode is not an intrinsic mode of these units or their constituents (nanorods and split-ring resonator), rather it is formed via capacitive coupling of the split-ring resonator of one unit with the nanorod of another unit. This leads to a unique charge distribution, generating a strong field accumulation at the center of the nanorod. We show that this assimilates a plasmon field profile similar to that of the intrinsic quadrupole mode of the nanorods, although it occurs at wavelengths longer than their dipole modes. Our results show that such a meta-mode generates a narrow dominant optical feature in the infrared range (∼1.5 µm) with significant immunity against the rotation of the lattices.

Semiconductor quantum dot super-emitters: spontaneous emission enhancement combined with suppression of defect environment using metal-oxide plasmonic metafilms.

We demonstrate that a metal-oxide plasmonic metafilm consisting of a Si/Al oxide junction in the vicinity of a thin gold layer can quarantine excitons in colloidal semiconductor quantum dots against their defect environments. This process happens while the plasmon fields of the gold layer enhance spontaneous emission decay rates of the quantum dots. We study the emission dynamics of such quantum dots when the distance between the Si/Al oxide junction and the gold thin layer is varied. The results show that for distances less than a critical value the lifetime of the quantum dots can be elongated while they experience intense plasmon fields. This suggests that the metal-oxide metafilm can keep photo-excited electrons in the cores of the quantum dots, suppressing their migration to the surface defect sites. This leads to suppression of Auger recombination, offering quantum dot super-emitters with emission that is enhanced not only by the plasmon fields (Purcell effect), but also by strong suppression of the non-radiative decay caused by the defect sites.

Biological sensing using hybridization phase of plasmonic resonances with photonic lattice modes in arrays of gold nanoantennas.

We study biological sensing using the hybridization phase of localized surface plasmon resonances (LSPRs) with diffraction modes (photonic lattice modes) in arrays of gold nanoantennas. We map the degree of the hybridization process using an embedding dielectric material (Si), identifying the critical thicknesses wherein the optical responses of the arrays are mainly governed by pure LSPRs (insignificant hybridization), Fano-type coupling of LSPRs with diffraction orders (hybridization state), and their intermediate state (hybridization phase). The results show that hybridization phase can occur with slight change in the refractive index (RI), leading to sudden reduction of the linewidth of the main spectral feature of the arrays by about one order of magnitude while it is shifted nearly 140 nm. These processes, which offer significant improvement in RI sensitivity and figure of merit, are utilized to detect monolayers of biological molecules and streptavidin-conjugated semiconductor quantum dots with sensitivities far higher than pure LSPRs. We further explore how these sensors can be used based on the uncoupled LSPRs by changing the polarization of the incident light.

Biological sensing and control of emission dynamics of quantum dot bioconjugates using arrays of long metallic nanorods.

We study biological sensing using plasmonic and photonic-plasmonic resonances of arrays of ultralong metallic nanorods and analyze the impact of these resonances on emission dynamics of quantum dot bioconjugates. We demonstrate that the LSPRs and plasmonic lattice modes of such array can be used to detect a single self-assembled monolayer of alkanethiol at the visible (550 nm) and near infrared (770 nm) range with well resolved shifts. We study adsorption of streptavidin-quantum dot conjugates to this monolayer, demonstrating that formation of nearly two dimensional arrays of quantum dots with limited emission blinking can lead to extra well-defined wavelength shifts in these modes. Using spectrally-resolved lifetime measurements we study the emission dynamics of such quantum dot bioconjugates within their monodispersed size distribution. We show that, despite their close vicinity to the nanorods, the rate of energy transfer from these quantum dots to nanorods is rather weak, while the plasmon field enhancement can be strong. Our results reveal that the nanorods present a strongly wavelength or size-dependent non-radiative decay channel to the quantum dot bioconjugates.