Publications by authors named "P Steinvurzel"

Fiber-optic parametric wavelength conversion (PWC) below the zero-dispersion wavelength of silica is typically constrained by the requirement of a small, tightly confined mode with anomalous dispersion to achieve phase matching. This limits the ability to power scale PWC at arbitrary wavelengths. However, the constraint is lifted for higher-order modes.

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Optical fibers have long been used to impose spatial coherence to shape free-space optical beams. Recent work has shown that one can use higher order fiber modes to create more exotic beam profiles. We experimentally generate optical bottles from Talbot imaging in the coherent superposition of two fiber modes excited with long period gratings, and obtain a 28 μm × 6 μm bottle with controlled contrast up to 10.

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We experimentally generate n=0 Bessel beams via higher-order cladding mode excitation with a long period fiber grating. Our method allows >99% conversion efficiency, wide or narrow conversion bandwidth, and accurate control of the number of rings in the beam. This latter property is equivalent to tuning the beam cone angle and allows for control of width and propagation distance of the center spot.

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Although optical tweezers based on far-fields have proven highly successful for manipulating objects larger than the wavelength of light, they face difficulties at the nanoscale because of the diffraction-limited focused spot size. This has motivated interest in trapping particles with plasmonic nanostructures, as they enable intense fields confined to sub-wavelength dimensions. A fundamental issue with plasmonics, however, is Ohmic loss, which results in the water, in which the trapping is performed, being heated and to thermal convection.

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We demonstrate that vertical silicon nanowires take on a surprising variety of colors covering the entire visible spectrum, in marked contrast to the gray color of bulk silicon. This effect is readily observable by bright-field microscopy, or even to the naked eye. The reflection spectra of the nanowires each show a dip whose position depends on the nanowire radii.

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