Browsing by Author "McClain, Michael J."

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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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    Ligand-Dependent Colloidal Stability Controls the Growth of Aluminum Nanocrystals
    (American Chemical Society, 2019) Clark, Benjamin D.; DeSantis, Christopher J.; Wu, Gang; Renard, David; McClain, Michael J.; Bursi, Luca; Tsai, Ah-Lim; Nordlander, Peter; Halas, Naomi J.; Laboratory for Nanophotonics
    The precise size- and shape-controlled synthesis of monodisperse Al nanocrystals remains an open challenge, limiting their utility for numerous applications that would take advantage of their size and shape-dependent optical properties. Here we pursue a molecular-level understanding of the formation of Al nanocrystals by titanium(IV) isopropoxide-catalyzed decomposition of AlH3ﾠin Lewis base solvents. As determined by electron paramagnetic resonance spectroscopy of intermediates, the reaction begins with the formation of Ti3+-AlH3ﾠcomplexes. Proton nuclear magnetic resonance spectroscopy indicates isopropoxy ligands are removed from Ti by Al, producing aluminum(III) isopropoxide and low-valent Ti3+ﾠcatalysts. These Ti3+ﾠspecies catalyze elimination of H2ﾠfrom AlH3ﾠinducing the polymerization of AlH3ﾠinto colloidally unstable low-valent aluminum hydride clusters. These clusters coalesce and grow while expelling H2ﾠto form colloidally stable Al nanocrystals. The colloidal stability of the Al nanocrystals and their size is determined by the molecular structure and density of coordinating atoms in the reaction, which is controlled by choice of solvent composition.
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    Monitoring Chemical Reactions with Terahertz Rotational Spectroscopy
    (American Chemical Society, 2018) Swearer, Dayne F.; Gottheim, Samuel; Simmons, Jay G.; Phillips, Dane J.; Kale, Matthew J.; McClain, Michael J.; Christopher, Phillip; Halas, Naomi J.; Everitt, Henry O.
    Rotational spectroscopy is introduced as a new in situ method for monitoring gas-phase reactants and products during chemical reactions. Exploiting its unambiguous molecular recognition specificity and extraordinary detection sensitivity, rotational spectroscopy at terahertz frequencies was used to monitor the decomposition of carbonyl sulfide (OCS) over an aluminum nanocrystal (AlNC) plasmonic photocatalyst. The intrinsic surface oxide on AlNCs is discovered to have a large number of strongly basic sites that are effective for mediating OCS decomposition. Spectroscopic monitoring revealed two different photothermal decomposition pathways for OCS, depending on the absence or presence of H2O. The strength of rotational spectroscopy is witnessed through its ability to detect and distinguish isotopologues of the same mass from an unlabeled OCS precursor at concentrations of <1 nanomolar or partial pressures of <10 μTorr. These attributes recommend rotational spectroscopy as a compelling alternative for monitoring gas-phase chemical reactants and products in real time.