An Optically Controlled Microscale Elevator Using Plasmonic Janus Particles.

In this article, we report how Janus particles, composed of a silica sphere with a gold half-shell, can be not only stably trapped by optical tweezers but also displaced controllably along the axis of the laser beam through a complex interplay between optical and thermal forces. Scattering forces orient the asymmetric particle, while strong absorption on the metal side induces a thermal gradient, resulting in particle motion. An increase in the laser power leads to an upward motion of the particle, while a decrease leads to a downward motion. We study this reversible axial displacement, including a hysteretic jump in the particle position that is a result of the complex pattern of a tightly focused laser beam structure above the focal plane. As a first application we simultaneously trap a spherical gold nanoparticle and show that we can control the distance between the two particles inside the trap. This photonic micron-scale "elevator" is a promising tool for thermal force studies, remote sensing, and optical and thermal micromanipulation experiments.

Synthesis and Crystal Structure of Gold Nanobelts.

Gold nanobelts were synthesized by the reduction of tetrachloroauric acid with ascorbic acid in the presence of the surfactants cetyltrimethylammonium bromide and sodium dodecylsulfate. The resulting structures have rectangular cross sectional dimensions that are tens of nanometers and lengths that are tens to hundreds of micrometers. We find that the nanobelt yield and resulting structures are very sensitive to temperature which is likely due to the transition of the surfactant solution from wormlike micelles to spherical micelles. The nanobelt crystal structure contains a mixture of face centered cubic and hexagonally close packed lattice phases that can be isolated and examined individually due to the unique nanobelt size and shape.

Gold nanobelts as high confinement plasmonic waveguides.

Plasmon propagation in thin plasmonic waveguides is strongly damped, making it difficult to study with diffraction-limited optics. Here we directly characterize plasmon propagation in gold nanobelts with incoherent light. The data indicate a short average propagation length of 0.94 µm but also reveal a weakly excited antisymmetric mode that has a propagation length greater than 10 µm with strong confinement of 2400 nm(2). These results demonstrate that high confinement and long propagation length can be achieved with thin plasmonic structures.

Structural transition in the surfactant layer that surrounds gold nanorods as observed by analytical surface-enhanced Raman spectroscopy.

Surface-enhanced Raman spectroscopy (SERS) of gold nanorods in cetyltrimethylammonium bromide solution has been used to analyze the interfacial surfactant structure based on the distance-dependent electromagnetic enhancement. The spectra were consistent with a surfactant bilayer oriented normal to the surface. As the surfactant concentration was reduced, a structural transition in the surfactant layer was observed through a sudden increase in the signal from the alkane chains. The structural transition was shown to influence the displacement of the surfactant layer by thiolated poly(ethylene glycol). The monodisperse and thoroughly characterized gold nanorod samples yield consistent enhancement factors that were compared to electromagnetic simulations.

A tunable plasmon resonance in gold nanobelts.

Plasmonic nanowires with sub-100-nm rectangular cross sections were found to exhibit a strong transverse plasmon peak at visible wavelengths. By correlating atomic force microscopy measurements of individual nanobelts with their dark-field scattering spectra, it is seen that the transverse peak tunes with cross-sectional aspect ratio. Simulations revealed that the scattering plasmonic modes are transverse antisymmetric excitations across the nanobelt width. Unlike larger diameter silver nanowires, these nanobelts exhibit sharp, tunable plasmon resonances similar to those of nanoparticles.

Hot plasmonic interactions: a new look at the photothermal efficacy of gold nanoparticles.

The photothermal (PT) outputs of individual gold nanoparticles (NP) were compared at room (cold) and high transient (hot) temperatures. High temperatures were induced in NPs by a single 0.5 ns laser pulse. All NPs with near-infrared plasmon resonances (rods, shells and bi-pyramids) exhibited a significant decrease in their photothermal output at the resonant wavelengths under high temperature, while non-resonant excitation of the same NPs provided several times higher PT efficacy of the hot NPs. This "inversion" of the PT efficacy of hot plasmonic NPs near their plasmon resonances might have been caused by damping of their resonances due to heating and surface melting. Therefore, photothermal output of plasmonic nanoparticles significantly depends upon their thermal state including the shift in excitation wavelength in hot nanoparticles. In particular, NPs with near-infrared resonances perform several times more efficiently at non-resonant excitation wavelengths rather than at the resonant ones.

Optically guided controlled release from liposomes with tunable plasmonic nanobubbles.

A new method of optically guided controlled release was experimentally evaluated with liposomes containing a molecular load and gold nanoparticles (NPs). NPs were exposed to short laser pulses to induce transient vapor bubbles around the NPs, plasmonic nanobubbles, in order to disrupt the liposome and eject its molecular contents. The release efficacy was tuned by varying the lifetime and size of the nanobubble with the fluence of the laser pulse. Optical scattering by nanobubbles correlated to the molecular release and was used to guide the release. The release of two fluorescent proteins from individual liposomes has been directly monitored by fluorescence microscopy, while the generation of the plasmonic nanobubbles was imaged and measured with optical scattering techniques. Plasmonic nanobubble-induced release was found to be a mechanical, nonthermal process that requires a single laser pulse and ejects the liposome contents within a millisecond timescale without damage to the molecular cargo and that can be controlled through the fluence of laser pulse.

The stabilization and targeting of surfactant-synthesized gold nanorods.

The strong cetyltrimethylammonium bromide (CTAB) surfactant responsible for the synthesis and stability of gold nanorod solutions complicates their biomedical applications. The critical parameter to maintain nanorod stability is the ratio of CTAB to nanorod concentration. The ratio is approximately 740,000 as determined by chloroform extraction of the CTAB from a nanorod solution. A comparison of nanorod stabilization by thiol-terminal PEG and by anionic polymers reveals that PEGylation results in higher yields and less aggregation upon removal of CTAB. A heterobifunctional PEG yields nanorods with exposed carboxyl groups for covalent conjugation to antibodies with the zero-length carbodiimide linker EDC. This conjugation strategy leads to approximately two functional antibodies per nanorod according to fluorimetry and ELISA assays. The nanorods specifically targeted cells in vitro and were visible with both two-photon and confocal reflectance microscopies. This covalent strategy should be generally applicable to other biomedical applications of gold nanorods as well as other gold nanoparticles synthesized with CTAB.