scholarly journals Solid-state tube wakefield accelerator using surface waves in crystals

2019 ◽  
Vol 34 (34) ◽  
pp. 1943009 ◽  
Author(s):  
Aakash A. Sahai ◽  
Toshiki Tajima ◽  
Peter Taborek ◽  
Vladimir D. Shiltsev

Solid-state or crystal acceleration has for long been regarded as an attractive frontier in advanced particle acceleration. However, experimental investigations of solid-state acceleration mechanisms which offer [Formula: see text] acceleration gradients have been hampered by several technological constraints. The primary constraint has been the unavailability of attosecond particle or photon sources suitable for excitation of collective modes in bulk crystals. Secondly, there are significant difficulties with direct high-intensity irradiation of bulk solids, such as beam instabilities due to crystal imperfections and collisions etc. Recent advances in ultrafast technology with the advent of submicron long electron bunches and thin-film compressed attosecond x-ray pulses have now made accessible ultrafast sources that are nearly the same order of magnitude in dimensions and energy density as the scales of collective electron oscillations in crystals. Moreover, nanotechnology enabled growth of crystal tube structures not only mitigates the direct high-intensity irradiation of materials, with the most intense part of the ultrafast source propagating within the tube but also enables a high degree of control over the crystal properties. In this work, we model an experimentally practicable solid-state acceleration mechanism using collective electron oscillations in crystals that sustain propagating surface waves. These surface waves are driven in the wake of a submicron long particle beam, ideally also of submicron transverse dimensions, in tube shaped nanostructured crystals with tube wall densities, [Formula: see text]. Particle-In-Cell (PIC) simulations carried out under experimental constraints demonstrate the possibility of accessing average acceleration gradients of several [Formula: see text] using the solid-state tube wakefield acceleration regime. Furthermore, our modeling demonstrates the possibility that as the surface oscillations and resultantly the surface wave transitions into a nonlinear or “crunch-in” regime under [Formula: see text], not only does the average gradient increase but strong transverse focusing fields extend down to the tube axis. This work thus demonstrates the near-term experimental realizability of Solid-State Tube Wakefield Accelerator (SOTWA). The ongoing progress in nanoengineering and attosecond source technology thereby now offers the potential to experimentally realize the promise of solid-state or crystal acceleration, opening up unprecedented pathways in miniaturization of accelerators.

Author(s):  
A. Martinez de la Ossa ◽  
R. W. Assmann ◽  
M. Bussmann ◽  
S. Corde ◽  
J. P. Couperus Cabadağ ◽  
...  

We present a conceptual design for a hybrid laser-driven plasma wakefield accelerator (LWFA) to beam-driven plasma wakefield accelerator (PWFA). In this set-up, the output beams from an LWFA stage are used as input beams of a new PWFA stage. In the PWFA stage, a new witness beam of largely increased quality can be produced and accelerated to higher energies. The feasibility and the potential of this concept is shown through exemplary particle-in-cell simulations. In addition, preliminary simulation results for a proof-of-concept experiment in Helmholtz-Zentrum Dresden-Rossendorf (Germany) are shown. This article is part of the Theo Murphy meeting issue ‘Directions in particle beam-driven plasma wakefield acceleration’.


Author(s):  
Aakash A. Sahai ◽  
Toshiki Tajima ◽  
Peter Taborek ◽  
Vladimir D. Shiltsev

2018 ◽  
Author(s):  
Francesco Salerno ◽  
Beth Rice ◽  
Julia Schmidt ◽  
Matthew J. Fuchter ◽  
Jenny Nelson ◽  
...  

<p>The properties of an organic semiconductor are dependent on both the chemical structure of the molecule involved, and how it is arranged in the solid-state. It is challenging to extract the influence of each individual factor, as small changes in the molecular structure often dramatically change the crystal packing and hence solid-state structure. Here, we use calculations to explore the influence of the nitrogen position on the charge mobility of a chiral organic molecule when the crystal packing is kept constant. The transfer integrals for a series of enantiopure aza[6]helicene crystals sharing the same packing were analysed in order to identify the best supramolecular motifs to promote charge carrier mobility. The regioisomers considered differ only in the positioning of the nitrogen atom in the aromatic scaffold. The simulations showed that even this small change in the chemical structure has a strong effect on the charge transport in the crystal, leading to differences in charge mobility of up to one order of magnitude. Some aza[6]helicene isomers that were packed interlocked with each other showed high HOMO-HOMO integrals (up to 70 meV), whilst molecules arranged with translational symmetry generally afforded the highest LUMO-LUMO integrals (40 - 70 meV). As many of the results are not intuitively obvious, a computational approach provides additional insight into the design of new semiconducting organic materials.</p>


2011 ◽  
Author(s):  
Piotr Macioł ◽  
Władysław Zalecki ◽  
Roman Kuziak ◽  
Aleksandra Jakubowicz ◽  
Stanisław Węglarczyk

Author(s):  
Marco Hornung ◽  
Sebastian Keppler ◽  
Alexander Kessler ◽  
Hartmut Liebetrau ◽  
Andreas Seidel ◽  
...  

2009 ◽  
Vol 625 ◽  
pp. 435-443 ◽  
Author(s):  
MARK A. KELMANSON

A novel pseudo-three-timescale asymptotic procedure is developed and implemented for obtaining accurate approximations to solutions of an evolution equation arising in thin-film free-surface viscous flow. The new procedure, which employs strained fast and slow timescales, requires considerably fewer calculations than its standard three-timescale counterpart employing fast, slow and slower timescales and may readily be applied to other evolution equations of fluid mechanics possessing wave-like solutions exhibiting exponential decay in amplitude and variations in phase over disparate timescales. The new method is validated on the evolution of free-surface waves on a thin, viscous film coating the exterior of a horizontal rotating cylinder and is shown to yield accurate solutions up to non-dimensional times exceeding by an order of magnitude those of previous related studies. Results of the new method applied to this test problem are demonstrated to be in excellent agreement, over large timescales, with those of corroborative spectrally accurate numerical integrations.


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