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Some preliminary results and experimental details of Near-field Scanning Optical Microscopy (NSOM) operation in liquids have been reported by us earlier(1-4). Here we present the first use of custom made polystyrene/poly (methyl methacrylate) (PMMA) optical fibers to assemble new NSOM probe/sensor for operation in liquids. Assembled NSOM probe has quite large quality factor Q ranging 2000-6000 in air(1), and 300-900 when immersed 0.2-0.3 mm deep into the water. Such montage demonstrates high mechanical durability permitting to scan different samples during many hours or even days, and overall low cost in comparison with NSOM probes based on glass optical fibers. A specially prepared optical fiber with 125 mu m diameter (from Paradigm Optics Company, USA) (polystyrene core diameter is 0.85 mu m, n(core) = 1.59 and PMMA cladding, n(core) = 1.49) was chemically etched using a 9: 1 mixture of dichloromethane and ethyl acetate(2). As result of the etching, a smooth and sharp tip is formed with a typical radius of the curvature equal to 50 - 170 nm. For completeness, earlier unpublished images of living Picocyanobacteria bacteria obtained using glass fiber-made NSOM probes are also presented.

Investigation of cell membrane structure and dynamics requires high spatial and temporal resolution. The spatial resolution of conventional light microscopy is limited due to the diffraction of light. However, recent developments in microscopy enabled us to access the nano-scale regime spatially, thus to elucidate the nanoscopic structures in the cellular membranes. In this review, we will explain the resolution limit, address the working principles of the most commonly used super-resolution microscopy techniques and summarise their recent applications in the biomembrane field.

In this paper, we demonstrate simultaneous AFM/NSOM using a dual-tip normal tuning-fork based scanning probe microscope. By scanning two SPM probes simultaneously, one dedicated for AFM with a standard tip diameter of 20 nm, and the second having a 150 nm aperture NSOM fiber with 200 nm thick gold coating, we combine the benefits of ∼20 nm spatial resolution from the AFM tip with the spectral information of a near-field optical probe. The combination of simultaneous dual-tip scanning enables us to decouple the requirements for high resolution topography and probe functionality. Our method represents a marked shift from previous applications of multi-probe SPM where essentially a pump-probe methodology is implemented in which one tip scans the area around the second. As a model system, we apply dual-tip AFM/NSOM scanning to a sample of spin-cast nano-clustered Lumogen dyes, which show remarkable brightness and photochemical stability. We observe morphology features with a resolution of 20 nm, and a near-field optical resolution of 150 nm, validating our approach.

Cellular uptake behavior of iron oxide nanoparticles is investigated using a transmission near-field scanning optical microscopy (NSOM) without the need of fluorescent labeling. By using the transmission NSOM system, we could simultaneously explore the near-field optical analysis of the cell interior and record the topographic information of the cell surface. The cell endocytosis of iron oxide nanoparticles by normal breast MCF10A cells is first studied by this transmission NSOM system, and this dual functional nanoscale-resolution microscopy shows the capability of mapping the spatial localization of nanoparticles in/outside cell surface without the need of fluorescence labeling. Nanoscale optical signature patterns for iron oxide nanoparticle-loaded vesicles inside the cells were observed and analyzed. © Springer Science+Business Media, LLC 2012.

Amplitude and phase measurements of the near-field generated by isolated subwavelength apertures in a gold film are presented. The near-field distribution of such a structure is complex and the measured signal strongly depends on the electric field components effectively detected by the experimental setup. By comparing this signal with 3D vectorial calculations we are able to determine which electric field components are effectively measured. The sensitivity of the phase distribution is key to this measurement. The proposed characterization technique should prove extremely useful to calibrate a Scanning near-field optical microscopy (SNOM) beforehand in order to retrieve quantitative information on the polarization of the field distribution under study.

Long regarded as a model system for studying insulator-to-metal phase transitions, the correlated electron material vanadium dioxide (VO$_2$) is now finding novel uses in device applications. Two of its most appealing aspects are its accessible transition temperature ($\sim$341 K) and its rich phase diagram. Strain can be used to selectively stabilize different VO$_2$ insulating phases by tuning the competition between electron and lattice degrees of freedom. It can even break the mesoscopic spatial symmetry of the transition, leading to a quasi-periodic ordering of insulating and metallic nanodomains. Nanostructuring of strained VO$_2$ could potentially yield unique components for future devices. However, the most spectacular property of VO$_2$ - its ultrafast transition - has not yet been studied on the length scale of its phase heterogeneity. Here, we use ultrafast near-field microscopy in the mid-infrared to study individual, strained VO$_2$ nanobeams on the 10 nm scale. We reveal a previously unseen correlation between the local steady-state switching susceptibility and the local ultrafast response to below-threshold photoexcitation. These results suggest that it may be possible to tailor the local photo-response of VO$_2$ using strain and thereby realize new types of ultrafast nano-optical devices.

Scanning near-field optical microscopy (SNOM or NSOM) is the technique with the highest lateral optical resolution available today, while infrared (IR) spectroscopy has a high chemical specificity. Combining SNOM with a tunable IR source produces a unique tool, IR-SNOM, capable of imaging distributions of chemical species with a 100 nm spatial resolution. We present in this paper boron nitride (BN) thin film images, where IR-SNOM shows the distribution of hexagonal and cubic phases within the sample. Exciting potential applications in biophysics and medical sciences are illustrated with SNOM images of the distribution of different chemical species within cells. We present in this article images with resolutions of the order of λ/60 with SNOM working with infrared light. With our SNOM setup, we routinely get optical resolutions between 50 and 150 nm, regardless of the wavelength of the light used to illuminate the sample.

Directional emission of electromagnetic radiation can be achieved using a properly shaped single antenna or a phased array of individual antennas. Control of the individual phases within an array enables scanning or other manipulations of the emission, and it is this property of phased arrays that makes them attractive in modern systems. Likewise, the propagation of surface plasmons at the interface between metal films and dielectric materials can be determined by shaping the individual surface nanostructures or via the phase control of individual elements in an array of such structures. Here, we demonstrate control of the propagation of surface plasmons within a linear array of nanostructures. The generic situation of plasmonic surface propagation that is different on both sides of a metal film provides a unique opportunity for such control: plasmons propagating on the slower side feed into the side with the faster propagation, creating a phased array of interfering antennas and thus controlling the directionality of the wake fields. We further show that by shaping the individual nanoantennas, we can generate an asymmetric propagation geometry. Surface plasmon propagation in a gold film on glass can be controlled by wake fields created using a linear array of nanostructures. Because they are small, directional and coherent, propagating surface plasmon polaritons are promising for next-generation photonic circuits. Yehiam Prior’s group at Weizmann Institute of Science, Israel, realized directional surface plasmon propagation in a thin gold layer on a glass substrate. The gold layer contained a line of 11 nanoscale holes, which provided coupling between plasmons traveling at different speeds in the gold–air and gold–glass interfaces above and below the gold film. The gold–glass plasmons traveled slower than the gold-air plasmons due to the higher effective refractive index of glass. Interference between the two sets of plasmons gave rise to a phase retardation effect and the appearance of directional plasma wake fields.

A novel technique of near field imaging has been advanced and used to measure free carrier diffusion length and study optical waveguiding in ZnO nanowires. The technique employs a near field scanning optical microscope (NSOM) and atomic force microscope (AFM) to optically and spatially map cathodoluminescence generated by a scanning electron microscope (SEM). The technique has been advanced from previous work on nanowires by the use of a higher resolution SEM and filtering approximately 90% of any background luminescent signal directly generated in the AFM/NSOM probe. For diameters between 250 nm and 800 nm, the diffusion length was found to vary with diameter. For diameters greater than 800 nm, the diffusion length is relatively constant. This is only the second such diameter dependence measurement for ZnO nanowires, and the only measurement for this nanowire diameter range. The full width at half maximum (FWHM) of the waveguiding output distribution from a single nanowire was found to be uncorrelated with the carrier excitation rate for a 60x increase in excitation rate. Luminescence of 380 nm was shown to propagate in the nanowire to a distance of 20-30 mm, indicating an absorption coefficient of ~2000 cm-1. http://archive.org/details/nearfieldimaging109457376 Lieutenant, United States Navy

International audience; This report presents the Apertureless Scanning Optical Near‐Field Microscope as a powerful tool for the characterization of modern optoelectronic and photonic components with sub‐wavelength resolution. We present an overview of the results we obtained in our laboratory over the past few years. By significant examples, it is shown that this specific probe microscopy allows for in situ local quantitative study of semiconductor lasers in operation, integrated optical waveguides produced by ion exchange (single channel or Y junction), and photonic structures.

In a recent letter Chicanne {\em et al.} [1] reported the experimental observation of the electromagnetic local density of states LDOS established by gold nanostructures. The obtained images have been compared with combinations of partial LDOSs defined in terms of the imaginary part of the Green-tensor ${\bf G}^I = [{\bf G}-{\bf G}^\dag]/(2i)$ calculated at the tip position. Moreover just this comparison was the criterion for the choice of the optimum tip design. These results support the point of view that ${\cal G}_{\bf u} =-({2 \omega}/{\pi c^2}) {\bf u} \cdot {\bf G}^I({\bf r}, {\bf r}, \omega) \cdot {\bf u}$ (${\bf u}$ is the unit vector used to define the effective dipole associated to the illuminating tip) is the key quantity to interpret SNOM images in analogy with the electronic LDOS measured by the scanning tunneling microscope (STM). Rigorous Green-tensor analysis shows that ${\cal G}_{\bf u}$ (that is also the key quantity determining spontaneous decay rates of molecular transitions) is not the correct key quantity, and that measurements in Ref. [1] should have been compared with a different quantity. Moreover the identification of ${\cal G}_{\bf u}$ with the detected SNOM signal can lead to unphysical results.

Polymers have the ability to conform to surface contours down to a few nanometres. We studied the filling of transparent epoxy-type EPON SU-8 into nanoscale apertures made in a thin metal film as a new method for polymer/metal near-field optical structures. Mould replica processes combining silicon micromachining with the photo-curable SU-8 offer great potential for low-cost nanostructure fabrication. In addition to offering a route for mass production, the transparent pyramidal probes are expected to improve light transmission thanks to a wider geometry near the aperture. By combining silicon MEMS, mould geometry tuning by oxidation, anti-adhesion coating by self-assembled monolayer and mechanical release steps, we propose an advanced method for near-field optical probe fabrication. The major improvement is the possibility to fabricate nanoscale apertures directly o­n wafer scale during the microfabrication process and not o­n free-standing tips. Optical measurements were performed with the fabricated probes. The full width half maximum after a Gaussian fit of the intensity profile indicates a lateral optical resolution of approximate to 60 nm.

The damping behavior of bent fiber near-field scanning optical microscopy (NSOM) probes operating in tapping mode oscillation is investigated in air and water. We show that the significant drop in probe quality factor Q, which occurs at the air-water interface, is due to meniscus damping. As the probe is immersed in water viscous damping adds to the meniscus damping. Damping effects which lead to a progressive drop in the peak tapping mode resonance frequency are accounted for by additional torsional modes of probe vibration. Understanding the damping processes should lead to the design of high sensitivity NSOM probes for scanning soft biological samples under liquid.