Laser-Driven Particle Acceleration - Improving Performance Through Smart Target Design

Laser-driven particle acceleration makes use of sub-picosecond, pulsed, high-power laser systems, capable of producing intensities ~10^{19} W/cm^2 at the laser focus to form plasmas, and use ultra-relativistic and nonlinear dynamics to produce quasistatic acceleration fields. This allows electrons to be accelerated to ~100 MeV over sub-centimetre distances, while protons may be accelerated to the ~10 MeV regime. In addition, novel sources of x-ray radiation become available with these schemes. The topics covered in this thesis focus mainly on target normal sheath acceleration of protons in the overdense plasma regime and laser wakefield acceleration of electrons in the underdense regime. An experimental approach leads to novel acceleration concepts and investigations on properties of new target designs. In the overdense plasma regime, hollow microspheres were found to have the potential to enhance the conversion of laser energy into proton energy. The microscopic structure of the material used as target has impact on electron beam filamentation during electron transport through the target bulk. Long-range order was found to result in smoother beams of TNSA-produced protons as compared to amorphous structures. In addition it was demonstrated that short pulse (fs) laser-solid interactions produce magnetic fields, the strength of which can reach 10 kT, mimicking astrophysical conditions. In the underdense regime, it was found that when tailored appropriately, density ramps can provide means of dividing the laser wakefield acceleration process into four steps: nonlinear laser evolution, trapping, bunch transfer into the second bucket, and acceleration, resulting in beams with reduced relative energy spread and divergence compared to self-injection by a nonlinear plasma wave. It was further shown that capillaries can be used to improve efficiency by guiding and refocusing the laser light onto the central axis. Short bursts of soft x-rays were produced inside capillaries. Finally, the use of an asymmetric laser field at the focus facilitated off-axis electron injection into the accelerating phase of a plasma wake oscillation and enhanced x-ray emission

Environment-Induced Surface Dynamics of a Biomimetic Ionomer Studied Using in Situ Second Harmonic Generation

The environmental-induced surface dynamics of the biomimetic phosphoryl choline (PC)-functionalized poly(trimethylene carbonate) ionomer has been studied and compared to its unfunctionalized counterpart using in situ second harmonic generation measurements. Whereas the nonpolar liquid n-hexane did not induce any surface dynamic processes in the ionomer under study, the presence of water initiated a Debye-type dynamic reaction at the surface of the PC ionomer, which had no equivalent in the unfunctionalized material. This first-order reaction was attributed to a surface enrichment process of the functionalized ionomer in the hydrophilic environment involving movement of the PC endgroups from aggregates in the bulk to the surface. The time constant of the process was found to be about 6 min, and the corresponding activation energy was 0.4 eV. The dehydration process of the PC-functionalized ionomer in nitrogen gas atmosphere could be described by two time constants, one slightly below 1 min and the other one just above 13 min. The results presented in this work show that SHG measurements are well suited for the study of polymer surface restructuring dynamics in response to environmental changes. Such information is very important for the successful design and implementation of biomimetic polymers intended for biomedical applications

Environment-Induced Surface Dynamics of a Biomimetic Ionomer Studied Using in Situ Second Harmonic Generation

The environmental-induced surface dynamics of the biomimetic phosphoryl choline (PC)-functionalized poly(trimethylene carbonate) ionomer has been studied and compared to its unfunctionalized counterpart using in situ second harmonic generation measurements. Whereas the nonpolar liquid n-hexane did not induce any surface dynamic processes in the ionomer under study, the presence of water initiated a Debye-type dynamic reaction at the surface of the PC ionomer, which had no equivalent in the unfunctionalized material. This first-order reaction was attributed to a surface enrichment process of the functionalized ionomer in the hydrophilic environment involving movement of the PC endgroups from aggregates in the bulk to the surface. The time constant of the process was found to be about 6 min, and the corresponding activation energy was 0.4 eV. The dehydration process of the PC-functionalized ionomer in nitrogen gas atmosphere could be described by two time constants, one slightly below 1 min and the other one just above 13 min. The results presented in this work show that SHG measurements are well suited for the study of polymer surface restructuring dynamics in response to environmental changes. Such information is very important for the successful design and implementation of biomimetic polymers intended for biomedical applications

Dispersion and monochromatization of x-rays using a beryllium prism

We demonstrate experimentally and numerically that an x-ray prism made of beryllium can be used to disperse and monochromatize x-rays. A polished beryllium cuboid was employed as refractive and dispersive optics. The results of a proof-of-principle experiment and methods of performance optimization are presented. The spatial separation of undulator harmonics and their subsequent selection using a slit are described. A numerical study, assuming realistic beam and beamline parameters, suggests that undulator harmonics can be spatially separated in the range from 3 keV to beyond 20 keV, while maintaining throughput above 50%. Refractive optics is particularly suitable for low-repetition-rate sources such as free-electron lasers and other LINAC-based short-pulse sources. (C) 2015 Optical Society of Americ

Effects of target pre-heating and expansion on terahertz radiation production from intense laser-solid interactions

The first experimental measurements of intense (∼7×1019 W cm−2) laser-driven terahertz (THz) radiation from a solid target which is preheated by an intense pulse of laser-accelerated protons is reported. The total energy of the THz radiation is found to decrease by approximately a factor of 2 compared to a cold target reference. This is attributed to an increase in the scale length of the preformed plasma, driven by proton heating, at the front surface of the target, where the THz radiation is generated. The results show the importance of controlling the preplasma scale length for THz production

Tunable mega-ampere electron current propagation in solids by dynamic control of lattice melt

The influence of lattice-melt-induced resistivity gradients on the transport of mega-ampere currents of fast electrons in solids is investigated numerically and experimentally using laser-accelerated protons to induce isochoric heating. Tailoring the heating profile enables the resistive magnetic fields which strongly influence the current propagation to be manipulated. This tunable laser-driven process enables important fast electron beam properties, including the beam divergence, profile and symmetry, to be actively tailored, and without recourse to complex target manufacture

Analysis of laser wakefield dynamics in capillary tubes

A general approach to the modifications of the spectrum of a laser pulse interacting with matter is elaborated and used for spectral diagnostics of laser wakefield generation in guiding structures. Analytical predictions of the laser frequency red shift due to the wakefield excited in a capillary waveguide are confirmed by self-consistent modeling results. The role of ionization blue shift, and nonlinear laser pulse and wakefield dynamics on the spectrum modification, is analyzed for recent experiments on plasma wave excitation by an intense laser pulse guided in hydrogen-filled glass capillary tubes up to 8 cm long. The dependence of the spectral frequency shift, measured as a function of filling pressure, capillary tube length and incident laser energy, is in excellent agreement with the simulation results, and the associated longitudinal accelerating field is in the range 1-10 GV m(-1)

FemtoMAX - An X-ray beamline for structural dynamics at the short-pulse facility of MAX IV

The FemtoMAX beamline facilitates studies of the structural dynamics of materials. Such studies are of fundamental importance for key scientific problems related to programming materials using light, enabling new storage media and new manufacturing techniques, obtaining sustainable energy by mimicking photosynthesis, and gleaning insights into chemical and biological functional dynamics. The FemtoMAX beamline utilizes the MAX IV linear accelerator as an electron source. The photon bursts have a pulse length of 100fs, which is on the timescale of molecular vibrations, and have wavelengths matching interatomic distances (Å). The uniqueness of the beamline has called for special beamline components. This paper presents the beamline design including ultrasensitive X-ray beam-position monitors based on thin Ce:YAG screens, efficient harmonic separators and novel timing tools.The FemtoMAX beamline facilitates studies of the structural dynamics of materials on the femtosecond timescale. The first commissioning results are presented