We have performed longitudinal magnetoresistance measurements on heavily n-doped silicon for donor concentrations exceeding the critical value for the metal-non-metal transition. The results are compared to those from a many-body theory where the don
or-electrons are assumed to reside at the bottom of the many-valley conduction band of the host. Good qualitative agreement between theory and experiment is obtained.
We employ ultra-broadband terahertz-midinfrared probe pulses to characterize the optical response of photoinduced charge-carrier plasmas in high-resistivity silicon in a reflection geometry, over a wide range of excitation densities (10^{15}-10^{19}
cm^{-3}) at room temperature. In contrast to conventional terahertz spectroscopy studies, this enables one to directly cover the frequency range encompassing the resultant plasma frequencies. The intensity reflection spectra of the thermalized plasma, measured using sum-frequency (up-conversion) detection of the probe pulses, can be modeled well by a standard Drude model with a density-dependent momentum scattering time of approx. 200 fs at low densities, reaching approx. 20 fs for densities of approx. 10^{19} cm^{-3}, where the increase of the scattering rate saturates. This behavior can be reproduced well with theoretical results based on the generalized Drude approach for the electron-hole scattering rate, where the saturation occurs due to phase-space restrictions as the plasma becomes degenerate. We also study the initial sub-picosecond temporal development of the Drude response, and discuss the observed rise in the scattering time in terms of initial charge-carrier relaxation, as well as the optical response of the photoexcited sample as predicted by finite-difference time-domain simulations.
We go beyond the approximate series-expansions used in the dispersion theory of finite size atoms. We demonstrate that a correct, and non-perturbative, theory dramatically alters the dispersion selfenergies of atoms. The non-perturbed theory gives as
much as 100% corrections compared to the traditional series expanded theory for the smaller noble gas atoms.
We calculate core-level spectra for pristine and doped free-standing graphene sheets. Instructions for how to perform the calculations are given in detail. Although pristine graphene is not metallic the core-level spectrum presents low-energy tailing
which is characteristic of metallic systems. The peak shapes vary with doping level in a characteristic way. The spectra are compared to experiments and show good agreement. We compare to two different pristine samples and to one doped sample. The pristine samples are one with quasi-free-standing epitaxial graphene on SiC obtained by hydrogen intercalation and one with a suspended graphene sheet. The doped sample is a gold supported graphene sheet. The gold substrate acts as an acceptor so the graphene sheet gets p-doped.
The Casimir-Polder force is an important long range interaction involved in adsorption and desorption of molecules in fluids. We explore Casimir-Polder interactions between methane molecules in water, and between a molecule in water near SiO2 and hex
ane surfaces. Inclusion of the finite molecular size in the expression for the Casimir-Polder energy leads to estimates of the dispersion contribution to the binding energies between molecules and between one molecule and a planar surface.
We present a variety of methods to derive the Casimir interaction in planar systems containing two-dimensional layers. Examples where this can be of use is graphene, graphene-like layers and two-dimensional electron gases. We present results for two
free standing layers and for one layer above a substrate. The results can easily be extended to systems with a larger number of layers.
We derive a general procedure for finding the electromagnetic normal modes in layered structures. We apply this procedure to planar, spherical and cylindrical structures. These normal modes are important in a variety of applications. They are the onl
y input needed in calculations of Casimir interactions. We present explicit expression for the condition for modes and Casimir energy for a large number of specific geometries. The layers are allowed to be two-dimensional so graphene and graphene-like sheets as well as two-dimensional electron gases can be handled within the formalism. Also forces on atoms in layered structures are obtained. One side-result is the van der Waals and Casimir-Polder interaction between two atoms.
