Browsing by Author "Schlather, Andrea E."

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    Aluminum Nanocrystals
    (American Chemical Society, 2015) McClain, Michael J.; Schlather, Andrea E.; Ringe, Emilie; King, Nicholas S.; Liu, Lifei; Manjavacas, Alejandro; Knight, Mark W.; Kumar, Ish; Whitmire, Kenton; Everitt, Henry O.; Nordlander, Peter; Halas, Naomi J.; Laboratory for Nanophotonics
    We demonstrate the facile synthesis of high purity aluminum nanocrystals over a range of controlled sizes from 70 to 220 nm diameter with size control achieved through a simple modification of solvent ratios in the reaction solution. The monodisperse, icosahedral, and trigonal bipyramidal nanocrystals are air-stable for weeks, due to the formation of a 2-4 nm thick passivating oxide layer on their surfaces. We show that the nanocrystals support size-dependent ultraviolet and visible plasmon modes, providing a far more sustainable alternative to gold and silver nanoparticles currently in widespread use.
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    High Chromaticity Aluminum Plasmonic Pixels for Active Liquid Crystal Displays
    (American Chemical Society, 2016) Olson, Jana; Manjavacas, Alejandro; Basu, Tiyash; Huang, Da; Schlather, Andrea E.; Zheng, Bob; Halas, Naomi; Nordlander, Peter; Link, Stephan; Laboratory for Nanophotonics
    Chromatic devices such as flat panel displays could, in principle, be substantially improved by incorporating aluminum plasmonic nanostructures instead of conventional chromophores that are susceptible to photobleaching. In nanostructure form, aluminum is capable of producing colors that span the visible region of the spectrum while contributing exceptional robustness, low cost, and streamlined manufacturability compatible with semiconductor manufacturing technology. However, individual aluminum nanostructures alone lack the vivid chromaticity of currently available chromophores because of the strong damping of the aluminum plasmon resonance in the visible region of the spectrum. In recent work, we showed that pixels formed by periodic arrays of Al nanostructures yield far more vivid coloration than the individual nanostructures. This progress was achieved by exploiting far-field diffractive coupling, which significantly suppresses the scattering response on the long-wavelength side of plasmonic pixel resonances. In the present work, we show that by utilizing another collective coupling effect, Fano interference, it is possible to substantially narrow theﾠshort-wavelengthﾠside of the pixel spectral response. Together, these two complementary effects provide unprecedented control of plasmonic pixel spectral line shape, resulting in aluminum pixels with far more vivid, monochromatic coloration across the entire RGB color gamut than previously attainable. We further demonstrate that pixels designed in this manner can be used directly as switchable elements in liquid crystal displays and determine the minimum and optimal numbers of nanorods required in an array to achieve good color quality and intensity.