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Abstract 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 + 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.

Abstract 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 × 1017W/cm2). The observed effect is attributed only to the field enhancing effects due to excited localized surface plasmons on the gold nanoparticles.

Temporal cleaning of high-power infrared (IR) pulses generated by a Ti:Sapphire system is demonstrated by the use of the Nonlinear Fourier Filtering (NFF) method. In a proof-of-principle experiment suppression of up to 1000 is achieved for the temporal pedestal prior to the main pulse, with a moderate (20-25%) overall throughput. This includes the same suppression ratio for the picosecond coherent pedestal in the direct vicinity of the main pulse. Based on the instantaneous, intensity-dependent and high-order switching characteristics of NFF, excellent pulse cleaning performance is observed. The efficient, high-contrast removal of the coherent pedestal from the foot of the main pulse even if its duration is shorter than 100 fs is compared with the capability of the plasma mirror technique. Calculations are also performed, supporting the experimentally observed sharp intensity dependence of the switching process, pointing out the dominant role of the ionization-based refractive index change.

In this work, the effects of femtosecond laser irradiation and doping with plasmonic gold nanorods on the degree of conversion ( DC ) of a urethane dimethacrylate (UDMA)-triethylene glycol dimethacrylate (TEGDMA) nanocomposite were investigated. The UDMA-TEGDMA photopolymer was prepared in a 3:1 weight ratio and doped with dodecanethiol- (DDT) capped gold nanorods of 25 × 75 or 25 × 85 nm nominal diameter and length. It was found that the presence of the gold nanorods alone (without direct plasmonic excitation) can increase the DC of the photopolymer by 6-15%. This increase was found to be similar to what could be achieved with a control heat treatment of 30 min at 180 °C. It was also shown that femtosecond laser impulses (795 nm, 5 mJ pulse energy, 50 fs pulse length, 2.83 Jcm -2 fluence), applied after the photopolymerization under a standard dental curing lamp, can cause a 2-7% increase in the DC of undoped samples, even after thermal pre-treatment. The best DC values (12-15% increase) were obtained with combined nanorod doping and subsequent laser irradiation close to the plasmon resonance peak of the nanorods (760-800 nm), which proves that the excited plasmon field can directly facilitate double bond breakage (without thermoplasmonic effects due to the short pulse length) and increase the crosslink density independently from the initial photopolymerization process.

We study experimentally the effect of linear plasma density gradients on the self-modulation of a 400 GeV proton bunch. Results show that a positive or negative gradient increases or decreases the number of microbunches and the relative charge per microbunch observed after 10 m of plasma. The measured modulation frequency also increases or decreases. With the largest positive gradient we observe two frequencies in the modulation power spectrum. Results are consistent with changes in wakefields' phase velocity due to plasma density gradients adding to the slow wakefields' phase velocity during self-modulation growth predicted by linear theory.

High order harmonics (HHG) were generated on noble gas cluster targets with different cluster sizes. The independently characterized cluster sources enabled experimental investigation of the recombination mechanism. HHG spectra were recorded for different backing pressures and gases (Ar, Xe) as a function of driver pulse ellipticity. Since the ellipticity-dependent HHG decay is essentially the same for the different gas-pressure pairs, we can conclude that the recombination process is dominated by atom-to-itself recollisions irrespective of cluster size and material.

The interaction of ultra-intense laser pulses with matter opened the way to generate the shortest light pulses available nowadays in the attosecond regime. Ionized solid surfaces, also called plasma mirrors, are promising tools to enhance the potential of attosecond sources in terms of photon energy, photon number and duration especially at relativistic laser intensities. Although the production of isolated attosecond pulses and the understanding of the underlying interactions represent a fundamental step towards the realization of such sources, these are challenging and have not yet been demonstrated. Here, we present laser-waveform-dependent high-order harmonic radiation in the extreme ultraviolet spectral range supporting well-isolated attosecond pulses, and utilize spectral interferometry to understand its relativistic generation mechanism. This unique interpretation of the measured spectra provides access to unrevealed temporal and spatial properties such as spectral phase difference between attosecond pulses and field-driven plasma surface motion during the process.