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  • Title: Ultrafast studies of gold, nickel, and palladium nanorods.
    Author: Sando GM, Berry AD, Owrutsky JC.
    Journal: J Chem Phys; 2007 Aug 21; 127(7):074705. PubMed ID: 17718625.
    Abstract:
    Steady state and ultrafast transient absorption studies have been carried out for gold, nickel, and palladium high aspect ratio nanorods. For each metal, nanorods were fabricated by electrochemical deposition into approximately 6 microm thick polycarbonate templates. Two nominal pore diameters(10 and 30 nm, resulting in nanorod diameters of about 40 and 60 nm, respectively) were used, yielding nanorods with high aspect ratios (>25). Static spectra of nanorods of all three metals reveal both a longitudinal surface plasmon resonance (SPR(L)) band in the mid-infrared as well as a transverse band in the visible for the gold and larger diameter nickel and palladium nanorods. The appearance of SPR(L) bands in the infrared for high aspect ratio metal nanorods and the trends in their maxima for the different aspect ratios and metals are consistent with calculations based on the Gans theory. For the gold and nickel samples, time resolved studies were performed with a subpicosecond resolution using 400 nm excitation and a wide range of probe wavelengths from the visible to the mid-IR as well as for infrared excitation (near 2000 cm(-1)) probed at 800 nm. The dynamics observed for nanorods of both metals and both diameters include transients due to electron-phonon coupling and impulsively excited coherent acoustic breathing mode oscillations, which are similar to those previously reported for spherical and smaller rod-shaped gold nanoparticles. The dynamics we observe are the same within the experimental uncertainty for 400 nm and infrared (5 microm) excitation probed at 800 nm. The transient absorption using 400 nm excitation and 800 nm probe pulses of the palladium nanorods also reveal coherent acoustic oscillations. The results demonstrate that the dynamics for high aspect ratio metal nanorods are similar to those for smaller nanoparticles.
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