Publications by authors named "Hai-Dong Deng"

The optomechanical interaction between a plasmonic nanocavity and a gold nanorod through optical forces is demonstrated. It is revealed that strong localized plasmon resonance mode hybridization induced by a gold nanorod results in the resonance mode of the nanocavity splitting into two different plasmon resonance modes (bonding plasmon resonance mode and antibonding plasmon resonance mode). When the whole system (gold nanorod and gold nanocavity) is excited at the antibonding plasmon mode, the gold nanorod can receive an optical pushing force and be pushed away from the gold nanocavity.

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We study the electromagnetic wave propagating in coupled monolayer graphene waveguide arrays (CMGWAs). It is found that Anderson localization exists when the disorder in the coupling strength between adjacent waveguides is introduced. We find that changing the statistical parameters of the disorder coupling strength between waveguides can be used to tailor the properties of the Anderson localization modes in the strong coupling region which is beyond the coupled-mode theory.

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Fano resonances in plasmonic systems have been proved to facilitate various sensing applications in the nanoscale. In this work, we propose an experimental scheme to realize a single protein sensing by utilizing its two-photon luminescence enhanced by a plasmonic Fano resonance system. The asymmetric gold hexamer supporting polarization-dependent Fano resonances and plasmonic modes without in-plane rotational symmetry is used as a referenced spatial coordinate for bio-sensing.

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Efficient three-photon luminescence (3PL) from a scintillating silicate glass co-doped with Gd(3+) and Tb(3+) was generated by using a focused femtosecond laser beam at 800 nm. Four emission bands centered at 496, 541, 583, and 620 nm were identified as the electronic transitions between the energy levels of Tb(3+) followed by three-photon absorption (3PA) in Gd(3+) and Tb(3+) and the resonant energy transfer from Gd(3+) to Tb(3+). More interestingly, a strong polarization dependence of the 3PL was observed and it is ascribed to the polarization dependent 3PA in Gd(3+) and Tb(3+) and/or the angular distribution of photogenerated electrons in the glass.

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We investigate systematically the competition between the second harmonic generation (SHG) and two-photon-induced luminescence (TPL) that are simultaneously present in Au nanoparticles excited by using a femtosecond (fs) laser. For a large-sized (length ~ 800 nm, diameter ~ 200 nm) Au nanorod, the SHG appears to be much stronger than the TPL. However, the situation is completely reversed when the Au nanorod is fragmented into many Au nanoparticles by the fs laser.

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We investigate the simultaneous trapping and melting of a large number of gold (Au) nanorods by using a single focused laser beam at 800 nm which is in resonance with the longitudinal surface plasmon resonance of Au nanorods. The trapping and melting processes were monitored by the two-photon luminescence of Au nanorods. A multi-ring-shaped pattern was observed in the steady state of the trapping process.

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We proposed a method to assemble microspheres into a three-dimensional crystal by utilizing the giant nonequilibrium depletion force produced by nanoparticles. Such assembling was demonstrated in a colloid formed by suitably mixing silica microspheres and magnetic nanoparticles. The giant nonequilibrium depletion force was generated by quickly driving magnetic nanoparticles out of the focusing region of a laser light through both optical force and thermophoresis.

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We demonstrate the switching of light in the near-infrared region (1.55 microm) through the manipulation of magnetic nanoparticles in a magnetic fluid by using another light in the visible region (0.532 microm).

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