RESUMO
We introduce a novel, gaseous target optical shaping laser set-up, capable to generate short scale length, near-critical target profiles via generated colliding blast waves. These profiles are capable to maintain their compressed density for several nanoseconds, being therefore ideal for laser-plasma particle acceleration experiments in the near critical density plasma regime. Our proposed method overcomes the laser-target synchronization limitations and delivers energetic protons, during the temporal evolution of the optically shaped profile, in a time window of approximately 2.5 ns. The optical shaping of the gas-jet profiles is optimised by MagnetoHydroDynamic simulations. 3D Particle-In-Cell models, adopting the spatiotemporal profile, simulate the 45 TW femtosecond laser plasma interaction to demonstrate the feasibility of the proposed proton acceleration set-up. The optical shaping of gas-jets is performed by multiple, nanosecond laser pulse generated blastwaves. This process results in steep gradient, short scale length plasma profiles, in the near critical density regime allowing operation at high repetition rates. Notably, the Magnetic Vortex Acceleration mechanism exhibits high efficiency in coupling the laser energy into the plasma in the optically shaped targets, resulting to collimated proton beams of energies up to 14 MeV.
RESUMO
High harmonic generation (HHG) is a central driver of the rapidly growing field of ultrafast science. We present a novel quasiphase-matching (QPM) concept with a dual-gas multijet target leading, for the first time, to remarkable phase control between multiple HHG sources (>2) within the Rayleigh range. The alternating jet structure with driving and matching zones shows perfect coherent buildup for up to six QPM periods. Although not in the focus of the proof-of-principle studies presented here, we achieved competitive conversion efficiencies already in this early stage of development.
RESUMO
The quantum phases of the electron paths driven by an ultrafast laser in high harmonic generation in an atomic gas depends linearly on the instantaneous cycle-averaged laser intensity. Using high laser intensities, a complete single ionisation of the atomic gas may occur before the laser pulse peak. Therefore, high harmonic generation could be localised only in a temporal window at the leading edge of laser pulse envelope. Varying the laser frequency chirp of an intense ultrafast laser pulse, the centre, and the width of the temporal window, that the high harmonic generation phenomenon occurs, could be controlled with high accuracy. This way, both the duration and the phase of the electron trajectories, that generate efficiently high harmonics, is fully controlled. A method of spectral control and selection of the high harmonic extreme ultraviolet light from distinct quantum paths is experimentally demonstrated. Furthermore, a phenomenological numerical model enlightens the physical processes that take place. This novel approach of the electron quantum path selection via laser chirp is a simple and versatile way of controlling the time-spectral characteristics of the coherent extreme ultraviolet light with applications in the fields of attosecond pulses and soft x-ray nano-imaging.
RESUMO
Nanoacoustic strains are generated in Silicon by chirped femtosecond laser pulses using thin Titanium films as transducers. We investigate the effect that the generating laser pulse chirp has on the amplitude of the induced strains, manifested as Brillouin oscillations observed in degenerate femtosecond pump-probe transient reflectivity measurements. The strain amplitude is larger when negatively chirped pulses are used, which is attributed to the more efficient conversion of laser pulse light into acoustic strain in the Titanium transducer. Our present studies clearly show that the dependence of the Brillouin amplitude and the lattice strain is a non-monotonous function of the laser chirp parameter. An optimum negative laser pulse chirp is found for which the strain amplitude is maximized. A detailed thermomechanical model satisfactorily supports the experimental findings. In such a way, it is possible to suppress or enhance the induced nanoacoustic strain amplitude, thus all-optically controlling it by at least a factor of two.