We have electrospun light-emitting nanofibers from ruthenium(II) tris(bipyridine)/polyethylene oxide mixtures. The electroluminescent fibers were deposited on gold interdigitated electrodes and lit in a nitrogen atmosphere. The fibers showed light emission at low operating voltages (3-4 V), with turn-on voltages approaching the band gap limit of the organic semiconductor. Because of the fiber size, emission from electrospun light-emitting nanofibers is confined to nanoscale dimensions, an attractive feature for sensing applications and lab-on-a-chip integration where highly localized excitation of molecules is required.

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Reconfigurable optical filters are of great importance for applications in optical communication and information processing. of particular interest are tuning techniques that take advantage of mechanical deformation of the devices, as they offer wider tuning range. Here we demonstrate reconfiguration of coupled photonic crystal nanobeam cavities by using optical gradient force induced mechanical actuation. Propagating waveguide modes that exist over a wide wavelength range are used to actuate the structures and control the resonance of localized cavity modes. using this all-optical approach, more than 18 linewidths of tuning range is demonstrated. using an on-chip temperature self-referencing method, we determine that 20% of the total tuning was due to optomechanical reconfiguration and the rest due to thermo-optic effects. By operating the device at frequencies higher than the thermal cutoff, we show high-speed operation dominated by just optomechanical effects. Independent control of mechanical and optical resonances of our structures is also demonstrated.

We examine size and frequency dependent gas damping of nanobeam resonators. We find an optimal beam width that maximizes the quality factor at atmospheric pressure, balancing the dissipation that scales with surface-to-volume ratio and dominates at small widths, against the interaction with the underlying substrate via the air that dominates the behavior of the wider devices. This latter interaction is found to affect the Knudsen number corresponding to a transition out of the molecular damping regime. We examine higher order modes and tune tension mechanically to vary the frequency of individual resonators, to resolve size and frequency effects.

We have developed an imaging system for 3D time-lapse polarization microscopy of living biological samples. Polarization imaging reveals the position, alignment and orientation of submicroscopic features in label-free as well as fluorescently labeled specimens. Optical anisotropies are calculated from a series of images where the sample is illuminated by light of different polarization states. Due to the number of images necessary to collect both multiple polarization states and multiple focal planes, 3D polarization imaging is most often prohibitively slow. Our MF-PolScope system employs multifocus optics to form an instantaneous 3D image of up to 25 simultaneous focal-planes. We describe this optical system and show examples of 3D multi-focus polarization imaging of biological samples, including a protein assembly study in budding yeast cells.