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In this brief report, we present laser induced breakdown spectroscopy (LIBS) evidence of deuterium (D) production in a 3:1 urethane dimethacrylate (UDMA) and triethylene glycol dimethacrylate (TEGDMA) polymer doped with resonant gold nanorods, induced by intense, 40 fs laser pulses. The in situ recorded LIBS spectra revealed that the D/(2D + H) increased to 4–8% in the polymer samples in selected events. The extent of transmutation was found to linearly increase with the laser pulse energy (intensity) between 2 and 25 mJ (up to 3 × 10 17 W/cm 2 ). The observed effect is attributed only to the field enhancing effects due to excited localized surface plasmons on the gold nanoparticles.

The NanoPlasmonic Laser Induced Fusion Energy (NAPLIFE) 1 project proposed fusion by regulating the laser light absorption via resonant nanorod antennas implanted into hydrogen rich urethane acrylate methacrylate (UDMA) and triethylene glycol dimethylacrylate (TEGDMA) copolymer targets. In part of the tests, boron-nitride (BN) was added to the polymer. Our experiments with resonant nanoantennas accelerated protons up to 225 keV energy. Some of these protons then led to p +  11 B fusion, indicated by the sharp drop of observed backward proton emission numbers at the 150 keV resonance energy of the reaction. The generation of alpha particles was verified by CR-39 (Columbia Resin #39) nuclear plastic track detectors.

High harmonics generation driven by 40 fs laser pulses is investigated in three different noble gases, both in gas and cluster regime depending on gas type and backing pressure. Pressure dependence of the harmonic intensity shows different scaling laws in case of cluster formation compared with monomer gas. Both the higher harmonic yield and the stronger spectral broadening of harmonics in xenon gas show the presence of clusters in the jet. The central wavelength of harmonics has a blue shift increasing with increasing laser intensity which is a consequence of free electron contribution to the phase matching.

The NanoPlasmonic Laser Induced Fusion Energy (NAPLIFE) project proposed fusion by regulating the laser light absorption via resonant nanorod antennas implanted into hydrogen rich urethane acrylate methacrylate (UDMA) and triethylene glycol dimethylacrylate (TEGDMA) copolymer targets. In part of the tests, boron-nitride (BN) was added to the polymer. Our experiments with resonant nanoantennas accelerated protons up to 225 keV energy. Some of these protons then led to p +  B fusion, indicated by the sharp drop of observed backward proton emission numbers at the 150 keV resonance energy of the reaction. The generation of alpha particles was verified by CR-39 (Columbia Resin #39) nuclear plastic track detectors.

We study experimentally the longitudinal and transverse wakefields driven by a highly relativistic proton bunch during self-modulation in plasma. We show that the wakefields’ growth and amplitude increase with increasing seed amplitude as well as with the proton bunch charge in the plasma. We study transverse wakefields using the maximum radius of the proton bunch distribution measured on a screen downstream from the plasma. We study longitudinal wakefields by externally injecting electrons and measuring their final energy. Measurements agree with trends predicted by theory and numerical simulations and validate our understanding of the development of self-modulation. Experiments were performed in the context of the Advanced Wakefield Experiment (AWAKE).

We present numerical simulations and experimental results of the self-modulation of a long proton bunch in a plasma with linear density gradients along the beam path. Simulation results agree with the experimental results reported [F. Braunmller, T. Nechaeva et al. (AWAKE Collaboration), Phys. Rev. Lett. 125, 264801 (2020)]: with negative gradients, the charge of the modulated bunch is lower than with positive gradients. In addition, the bunch modulation frequency varies with gradient. Simulation results show that dephasing of the wakefields with respect to the relativistic protons along the plasma is the main cause for the loss of charge. The study of the modulation frequency reveals details about the evolution of the self-modulation process along the plasma. In particular for negative gradients, the modulation frequency across time-resolved images of the bunch indicates the position along the plasma where protons leave the wakefields. Simulations and experimental results are in excellent agreement.

Plasma wakefield dynamics over timescales up to 800 ps, approximately 100 plasma periods, are studied experimentally at the Advanced Wakefield Experiment (AWAKE). The development of the longitudinal wakefield amplitude driven by a self-modulated proton bunch is measured using the external injection of witness electrons that sample the fields. In simulation, resonant excitation of the wakefield causes plasma electron trajectory crossing, resulting in the development of a potential outside the plasma boundary as electrons are transversely ejected. Trends consistent with the presence of this potential are experimentally measured and their dependence on wakefield amplitude are studied via seed laser timing scans and electron injection delay scans.

The NanoPlasmonic Laser Induced Fusion Energy (NAPLIFE) project proposed fusion by regulating the laser light absorption via resonant nanorod antennas implanted into hydrogen rich urethane acrylate methacrylate (UDMA) and triethylene glycol dimethylacrylate (TEGDMA) copolymer targets. In part of the tests, boron-nitride (BN) was added to the polymer. Our experiments with resonant nanoantennas accelerated protons up to 225 keV energy. Some of these protons then led to p + 11B fusion, indicated by the sharp drop of observed backward proton emission numbers at the 150 keV resonance energy of the reaction. The generation of alpha particles was verified by CR-39 (Columbia Resin #39) nuclear plastic track detectors.

We study the propagation of 0.05-1 TW power, ultrafast laser pulses in a 10 meter long rubidium vapor cell. The central wavelength of the laser is resonant with the \\(D_2\\) line of rubidium and the peak intensity in the \\(10^{12}-10^{14} ~W/cm^2\\) range, enough to create a plasma channel with single electron ionization. We observe the absorption of the laser pulse for low energy, a regime of transverse confinement of the laser beam by the strong resonant nonlinearity for higher energies and the transverse broadening of the output beam when the nonlinearity is saturated due to full medium ionization. We compare experimental observations of transmitted pulse energy and transverse fluence profile with the results of computer simulations modeling pulse propagation. We find a qualitative agreement between theory and experiment that corroborates the validity of our propagation model. While the quantitative differences are substantial, the results show that the model can be used to interpret the observed phenomena in terms of self-focusing and channeling of the laser pulses by the saturable nonlinearity and the transparency of the fully ionized medium along the propagation axis.

In this brief report, we present laser induced breakdown spectroscopy (LIBS) evidence of deuterium (D) production in a 3:1 urethane dimethacrylate (UDMA) and triethylene glycol dimethacrylate (TEGDMA) polymer doped with resonant gold nanorods, induced by intense, 40 fs laser pulses. The in situ recorded LIBS spectra revealed that the D/(2D+H) increased to 4-8% in the polymer samples in selected events. The extent of transmutation was found to linearly increase with the laser pulse energy (intensity) between 2 and 25 mJ (up to 3x10^17 W/cm). The observed effect is attributed only to the field enhancing effects due to excited localized surface plasmons on the gold nanoparticles.