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The detection of a few molecules in a highly diluted solution is of paramount interest in fields including biomedicine, safety and eco-pollution in relation to rare and dangerous chemicals. Nanosensors based on plasmonics are promising devices in this regard, in that they combine the features of high sensitivity, label-free detection and miniaturization. However, plasmonic-based nanosensors, in common with general sensors with sensitive areas on the scale of nanometres, cannot be used directly to detect molecules dissolved in femto- or attomolar solutions. In other words, they are diffusion-limited and their detection times become impractical at such concentrations. In this Article, we demonstrate, by combining super-hydrophobic artificial surfaces and nanoplasmonic structures, that few molecules can be localized and detected even at attomolar (10−18 mol l−1) concentration. Moreover, the detection can be combined with fluorescence and Raman spectroscopy, such that the chemical signature of the molecules can be clearly determined

Self-propelling bacteria are a nanotechnology dream. These unicellular organisms are not just capable of living and reproducing, but they can swim very efficiently, sense the environment, and look for food, all packaged in a body measuring a few microns. Before such perfect machines can be artificially assembled, researchers are beginning to explore new ways to harness bacteria as propelling units for microdevices. Proposed strategies require the careful task of aligning and binding bacterial cells on synthetic surfaces in order to have them work cooperatively. Here we show that asymmetric environments can produce a spontaneous and unidirectional rotation of nanofabricated objects immersed in an active bacterial bath. The propulsion mechanism is provided by the self-assembly of motile Escherichia coli cells along the rotor boundaries. Our results highlight the technological implications of active matter's ability to overcome the restrictions imposed by the second law of thermodynamics on equilibrium passive fluids.biological motors | self-propulsion | ratchet effect

The fields of plasmonics, Raman spectroscopy and atomic force microscopy have recently undergone considerable development, but independently of one another. By combining these techniques, a range of complementary information could be simultaneously obtained at a single molecule level. Here, we report the design, fabrication and application of a photonic-plasmonic device that is fully compatible with atomic force microscopy and Raman spectroscopy. Our approach relies on the generation and localization of surface plasmon polaritons by means of adiabatic compression through a metallic tapered waveguide to create strongly enhanced Raman excitation in a region just a few nanometres across. The tapered waveguide can also be used as an atomic force microscope tip. Using the device, topographic, chemical and structural information about silicon nanocrystals may be obtained with a spatial resolution of 7 nm.

Three-dimensional vertical micro- and nanostructures can enhance the signal quality of multielectrode arrays and promise to become the prime methodology for the investigation of large networks of electrogenic cells. So far, access to the intracellular environment has been obtained via spontaneous poration, electroporation, or by surface functionalization of the micro/nanostructures; however, these methods still suffer from some limitations due to their intrinsic characteristics that limit their widespread use. Here, we demonstrate the ability to continuously record both extracellular and intracellular-like action potentials at each electrode site in spontaneously active mammalian neurons and HL-1 cardiac-derived cells via the combination of vertical nanoelectrodes with plasmonic optoporation. We demonstrate long-term and stable recordings with a very good signal-to-noise ratio. Additionally, plasmonic optoporation does not perturb the spontaneous electrical activity; it permits continuous recording even during the poration process and can regulate extracellular and intracellular contributions by means of partial cellular poration.

The direct conversion of light into work allows the driving of micron-sized motors in a contactless, controllable and continuous way. Light-to-work conversion can involve either direct transfer of optical momentum or indirect opto-thermal effects. Both strategies have been implemented using different coupling mechanisms. However, the resulting efficiencies are always very low, and high power densities, generally obtained by focused laser beams, are required. Here we show that microfabricated gears, sitting on a liquid–air interface, can efficiently convert absorbed light into rotational motion through a thermocapillary effect. We demonstrate rotation rates up to 300 r.p.m. under wide-field illumination with incoherent light. Our analysis shows that thermocapillary propulsion is one of the strongest mechanisms for light actuation at the micron- and nanoscale.

Plasmonic nanostar-dimers, decoupled from the substrate, have been fabricated by combining electron-beam lithography and reactive-ion etching techniques. The 3D architecture, the sharp tips of the nanostars and the sub-10 nm gap size promote the formation of giant electric-field in highly localized hot-spots. The single/few molecule detection capability of the 3D nanostar-dimers has been demonstrated by Surface-Enhanced Raman Scattering.

We demonstrate an innovative concept for nanoscale electro-optic switching. It exploits the frequency shift of a narrow-band Fano resonance mode in a plasmonic planar metamaterial induced by a change in the dielectric properties of an adjacent chalcogenide glass layer. An electrically stimulated transition between amorphous and crystalline forms of the glass brings about a 150 nm shift in the near-infrared resonance providing transmission modulation with a contrast ratio of 4:1 in a device of subwavelength thickness. © 2010 American Institute of Physics. ͓doi:10.1063/1.3355544͔ Nanophotonic applications, in particular, photonic data processing circuits, require active devices of subwavelength dimensions. However, electro-optic modulation of light in a device of nanoscale thickness is not a trivial problem. In conventional modulators exploiting the Pockels or Kerr effects, the polarization switching involved requires the interference of two propagating modes to develop over distances far in excess of the wavelength of light. The dimensions of such modulators in the propagation direction are often in the centimeter range. Signal modulation via control of the waveguide absorption coefficient or refractive index is another possibility. However, this approach also requires substantial propagation lengths over which an amplitude or phase change accumulates, or it involves interferometric arrangements that are inherently longer than the wavelength of light. It has been suggested that strong signal modulation may be achieved in nanophotonic devices, despite very short propagation lengths, through the use of materials that show a substantial change in absorption or refraction in response to a control excitation: the relative change in the real and/or imaginary parts of the refractive coefficient must be of the order of unity and this can only be achieved in metals, where phase changes can bring about significant changes in optical properties. Such functionality has been extensively demonstrated with elemental gallium, which can exist in phases with radically different optical properties. In this case, phase changes lead to a modification of the plasmon and interband absorption to provide a platform for nanoscale active devices. 1-3Here we demonstrate another approach to nanoscale electro-optic modulation that relies not on absorption modulation but rather on a change in the refraction of a material associated with a control-input-induced phase change. In a layer of nanoscale thickness, such a refractive index change would be insufficient to noticeably modulate the intensity or phase of a transmitted wave. However, we demonstrate that by combining a nanoscale layer of phase-change material with a planar plasmonic metamaterial ͑Fig. 1͒ one can exploit the fact that the position of narrow resonant absorption lines in certain metamaterials are strongly dependent on the dielectric environment; switching the dielectric layer in contact with such a metamaterial produces a massive change in its resonance frequency. Importantly, ...