14,878 research outputs found
Helices at Interfaces
Helically coiled filaments are a frequent motif in nature. In situations
commonly encountered in experiments coiled helices are squeezed flat onto two
dimensional surfaces. Under such 2-D confinement helices form "squeelices" -
peculiar squeezed conformations often resembling looped waves, spirals or
circles. Using theory and Monte-Carlo simulations we illuminate here the
mechanics and the unusual statistical mechanics of confined helices and show
that their fluctuations can be understood in terms of moving and interacting
discrete particle-like entities - the "twist-kinks". We show that confined
filaments can thermally switch between discrete topological twist quantized
states, with some of the states exhibiting dramatically enhanced
circularization probability while others displaying surprising
hyperflexibility
Prompt Beta Spectroscopy as a Diagnostic for Mix in Ignited NIF Capsules
The National Ignition Facility (NIF) technology is designed to drive
deuterium-tritium (DT) internal confinement fusion (ICF) targets to ignition
using indirect radiation from laser beam energy captured in a hohlraum.
Hydrodynamical instabilities at interfaces in the ICF capsule leading to mix
between the DT fue l and the ablator shell material are of fundamental physical
interest and can affect the performance characteristics of the capsule. In this
Letter we describe new radiochemical diagnostics for mix processes in ICF
capsules with plastic or Be (0.9%Cu) ablator shells. Reactions of high-energy
tritons with shell material produce high-energy -emitters.
We show that mix between the DT fuel and the shell material enhances
high-energy prompt beta emission from these reactions by more than an order of
magnitude over that expected in the absence of mix
Exactly soluble model of interacting electrons
Journal ArticleWe diagonalize a many-fermion Hamiltonian consisting of terms quadratic as well as quartic in the field operators. A dual spectrum of eigenstates is an interesting result. We also derive a formula for obtaining the free energy at finite temperature
Instantaneous ionization rate as a functional derivative
We describe an approach defining instantaneous ionization rate (IIR) as a
functional derivative of the total ionization probability. The definition is
based on physical quantities which are directly measurable, such as the total
ionization probability and the waveform of the pulse. The definition is,
therefore, unambiguous and does not suffer from gauge non-invariance. We
compute IIR by solving numerically the time-dependent Schrodinger equation for
the hydrogen atom in a strong laser field. We find that the IIR lags behind the
electric field, but this lag is entirely due to the long tail effect of the
Coulomb field. In agreement with the previous results using attoclock
methodology, therefore, the IIR we define does not show measurable delay in
strong field tunnel ionization
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