Surface recoil force on dielectric nanoparticle enhancement via graphene acoustic surface plasmon excitation: non-local effect consideration.

Controlling optomechanical interactions at sub-wavelength levels is of great importance in academic science and nanoparticle manipulation technologies. This Letter focuses on the improvement of the recoil force on nanoparticles placed close to a graphene-dielectric-metal structure. The momentum conservation involving the non-symmetric excitation of acoustic surface plasmons (ASPs), via near-field circularly polarized dipolar scattering, implies the occurrence of a huge momentum kick on the nanoparticle.

Graphene surface modes enabling terahertz pulling force.

Plasmonic substrates are widely reported for their use in the manipulation of sub-wavelength particles. Here we analyze the optical force in the terahertz (THz) spectrum acting on a dielectric nanoparticle when located close to a graphene monolayer. When lying on a dielectric planar substrate, the graphene sheet enables the nano-sized scatterer to excite a surface plasmon (SP) well confined on the dielectric surface.

Giant terahertz pulling force within an evanescent field induced by asymmetric wave coupling into radiative and bound modes.

Manipulation of nano-scale objects by engineering the electromagnetic waves in the environment medium is pivotal for several particle handling techniques using optical resonators, waveguiding, and plasmonic devices. In this Letter, we theoretically demonstrate the possibility of engineering a compact and tunable plasmon-based terahertz (THz) tweezer using a graphene monolayer that is deposited on a high-index dielectric substrate. When a nanoparticle located in a vacuum in the vicinity of the graphene monolayer is illuminated under total internal reflection, as light is launched from the substrate, such a device is shown to be capable of inducing an enhanced rotating dipole in the nanoparticle thus enabling asymmetric, directional near-field coupling into the graphene plasmon mode and the radiative modes in the substrate.