91 research outputs found
Oscillatory Size-Dependence of the Surface Plasmon Linewidth in Metallic Nanoparticles
We study the linewidth of the surface plasmon resonance in the optical
absorption spectrum of metallic nanoparticles, when the decay into
electron-hole pairs is the dominant channel. Within a semiclassical approach,
we find that the electron-hole density-density correlation oscillates as a
function of the size of the particles, leading to oscillations of the
linewidth. This result is confirmed numerically for alkali and noble metal
particles. While the linewidth can increase strongly, the oscillations persist
when the particles are embedded in a matrix.Comment: RevTeX4, 5 pages, 2 figures, final versio
Ultrathin 2 nm gold as ideal impedance-matched absorber for infrared light
Thermal detectors are a cornerstone of infrared (IR) and terahertz (THz)
technology due to their broad spectral range. These detectors call for suitable
broad spectral absorbers with minimalthermal mass. Often this is realized by
plasmonic absorbers, which ensure a high absorptivity butonly for a narrow
spectral band. Alternativly, a common approach is based on impedance-matching
the sheet resistance of a thin metallic film to half the free-space impedance.
Thereby, it is possible to achieve a wavelength-independent absorptivity of up
to 50 %, depending on the dielectric properties of the underlying substrate.
However, existing absorber films typicallyrequire a thickness of the order of
tens of nanometers, such as titanium nitride (14 nm), whichcan significantly
deteriorate the response of a thermal transducers. Here, we present the
application of ultrathin gold (2 nm) on top of a 1.2 nm copper oxide seed layer
as an effective IR absorber. An almost wavelength-independent and long-time
stable absorptivity of 47(3) %, ranging from 2 m to 20 m, could be
obtained and is further discussed. The presented gold thin-film represents
analmost ideal impedance-matched IR absorber that allows a significant
improvement of state-of-the-art thermal detector technology
Diffusion of gold nanoclusters on graphite
We present a detailed molecular-dynamics study of the diffusion and
coalescence of large (249-atom) gold clusters on graphite surfaces. The
diffusivity of monoclusters is found to be comparable to that for single
adatoms. Likewise, and even more important, cluster dimers are also found to
diffuse at a rate which is comparable to that for adatoms and monoclusters. As
a consequence, large islands formed by cluster aggregation are also expected to
be mobile. Using kinetic Monte Carlo simulations, and assuming a proper scaling
law for the dependence on size of the diffusivity of large clusters, we find
that islands consisting of as many as 100 monoclusters should exhibit
significant mobility. This result has profound implications for the morphology
of cluster-assembled materials
Untersuchung ĂĽber MaĂźnahmen zur Verbesserung der Software-Produktion. Bd.4: Einsatzerfahrungen mit Standard-Anwendungs-Software und Anforderungen an ein Bausteinkonzept
Local correlation of photoemission electron microscopy and STM at a defined cluster substrate system
Electron dynamics in supported metal nanoparticles: relaxation and charge transfer studied by time-resolved photoemission
Pfeiffer W, Kennerknecht C, Merschdorf M. Electron dynamics in supported metal nanoparticles: relaxation and charge transfer studied by time-resolved photoemission. Applied Physics A. 2004;78(7):1011-1028.Resonant excitation of the plasmon polariton in supported nanoparticles leads to a strong enhancement of the multiphoton photoemission yield and consequently, the total yield is dominated by the emission from the nanoparticles although they cover only a minor fraction of the surface. This allows investigation of the electron dynamics in supported nanoparticles, directly in the time domain. Here, Ag nanoparticles grown on graphite are used to demonstrate that the transient shape of the photoemission spectrum in time-resolved two-color multiphoton photoemission spectroscopy, reveals the electron relaxation within the nanoparticle, and the dynamic charge transfer between substrate and nanoparticle. The photoemission spectra map the transient electron energy distribution and exhibit a transient shift that is attributed to a dynamic charging of the nanoparticle. The comparison with model calculations comprising the full relaxation cascade in the nanoparticle and substrate, shows that the dynamic charge transfer accounts for almost half of the total deposited energy in the nanoparticle
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