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High-intensity ultrashort laser pulses focused on metal targets readily generate hot dense plasmas which accelerate ions efficiently and can pave way to compact table-top accelerators. Laser-driven ion acceleration studies predominantly focus on protons, which experience the maximum acceleration owing to their highest charge-to-mass ratio. The possibility of tailoring such schemes for the preferential acceleration of a particular ion species is very much desired but has hardly been explored. Here, we present an experimental demonstration of how the nanostructuring of a copper target can be optimized for enhanced carbon ion acceleration over protons or Cu-ions. Specifically, a thin (≈0.25 μm) layer of 25–30 nm diameter Cu nanoparticles, sputter-deposited on a polished Cu-substrate, enhances the carbon ion energy by about 10-fold at a laser intensity of 1.2×10 18   W/cm 2 . However, particles smaller than 20 nm have an adverse effect on the ion acceleration. Particle-in-cell simulations provide definite pointers regarding the size of nanoparticles necessary for maximizing the ion acceleration. The inherent contrast of the laser pulse is found to play an important role in the species selective ion acceleration.

La2NiMnO6 (LNMO) was prepared by a combustion method followed by heating at high temperature. Subsequently, the preformed LNMO was annealed in air, oxygen, or N2 atmosphere and characterized by powder x-ray diffraction (XRD), neutron diffraction, superconducting quantum interference device magnetometry, and dielectric analysis. Structural studies by XRD and neutron diffraction revealed the coexistence of partially cation disordered monoclinic (31%) and rhombohedral (69%) phases in the sample annealed in air. However, the sample annealed in oxygen shows about 50:50% of monoclinic and rhombohedral phases. Relaxor-like behavior with relative permittivity of the order of 104 was observed in the sample annealed in air, while relative permittivity decreases to about 200 in samples annealed in oxygen atmosphere. The magnetic properties indicate a well-defined ferromagnetic phase in the oxygen-annealed sample compared to a feeble ferromagnetic signature in the air-annealed one. The dielectric and ferromagnetism of LNMO samples have been related to formation and annihilation of oxygen vacancies.

Carbon aerogel is a promising material for electrochemical double layer capacitors. In this paper carbon aerogels prepared by subcritical drying method are investigated for the change in the structure and surface properties at different pyrolysis temperatures. The important relations between structure, morphology, surface area and electrical properties were studied using X-ray diffraction (XRD), Fourier transform infrared (FTIR) spectroscopy, scanning electron microscopy (SEM), surface area measurement and cyclic voltametry. It is shown that structure and the surface functional groups play important role in enhancement of electrochemical capacitance. The specific capacitance achieved was 114 F/gm which is quite large value for subcritically prepared carbon aerogels without any kind of activation process.

The impact of nano-structured surfaces on particle generation from ultrashort intense laser produced plasmas is presented over an intensity range of 1015–1017 Wcm−2. The nano-structured surface evidently produces hotter plasma but does not lead to the generation of hotter ions, a counterintuitive result based on present understanding of plasma expansion mechanism. Although the total ion flux and energy is more in the case of structured surfaces, the average energy of the projectiles is found to be lower than that from polished surfaces. The nano-structured surface shows preferential enhancement of lower energy ions and an intensity dependent divergence of the ejected particles.

Presence of nano-particles on target surface has been observed to lead to increased laser absorption of laser pulse in plasma. Therefore, a coating of nano-particles on foil targets could lead to an enhanced ablative acceleration. The work presented in this paper concerns this possibility. The results of experiments performed with PALS laser system (125 J, ∼250 ps at 1.3 μm) with a focused intensity of about 1014 W/cm2 are presented. 15 μm thick Polyethylene teraphthalate (C10 H8 O4)n or PET foils show an almost 40% increase in target movement when coated with a layer of gold nano-particles. Comparison between targets with coating of bulk gold and nano-gold shows about 15% higher target movement in gold nano-particle coated PET targets as compared to bulk gold coating. This result is a clear indication of enhanced laser energy absorption in targets with nano-structured surface of gold. We also present evidence to show the effect of nano-particle coating on lateral thermal conduction.

In this paper, we present the results of studies on ion emission characteristics of a laser plasma produced from a copper nano-particle layer of 1–3 µm thickness coated over polished surface of a solid copper target. Laser intensity of 1013–1014 W/cm2 was produced on the targets by a 2 J Nd:glass laser having a variable pulse duration of 300–800 ps. Nano-particle size was in the range of 15–25 nm. Ion emission from the nano-particle plasma was compared with plasma generated from a polished copper target. Ion emission from the nano-structured target was observed to depend on the polarization of the incident laser beam. This effect was stronger for a shorter laser pulse. X-ray emission was measured in the soft and hard X-ray region (0.7 to 8 keV) using various X-ray filters. A nano-particle coated target is found to yield a larger flux as well as velocity of ions as compared to polished target when the laser polarization is parallel to the plane containing target normal and detector axis. However, no X-ray enhancement has been observed in the wavelength range 1.5 to 20 Å.

High-intensity ultrashort laser pulses focused on metal targets readily generate hot dense plasmas which accelerate ions efficiently and can pave way to compact table-top accelerators. Laser-driven ion acceleration studies predominantly focus on protons, which experience the maximum acceleration owing to their highest charge-to-mass ratio. The possibility of tailoring such schemes for the preferential acceleration of a particular ion species is very much desired but has hardly been explored. Here, we present an experimental demonstration of how the nanostructuring of a copper target can be optimized for enhanced carbon ion acceleration over protons or Cu-ions. Specifically, a thin (≈0.25 μm) layer of 25–30 nm diameter Cu nanoparticles, sputter-deposited on a polished Cu-substrate, enhances the carbon ion energy by about 10-fold at a laser intensity of 1.2×10 18   W/cm 2 . However, particles smaller than 20 nm have an adverse effect on the ion acceleration. Particle-in-cell simulations provide definite pointers regarding the size of nanoparticles necessary for maximizing the ion acceleration. The inherent contrast of the laser pulse is found to play an important role in the species selective ion acceleration.

Proton beam lithography has made it possible to make various types of 3D-structures in polymers. Usually PMMA, SU-8, PS polymers have been used as resist materials for lithographic purpose. Microbeam irradiation effects on poly-tert-butyl-acrylate (PtBA) polymer using 20 MeV proton microbeam are reported. Preliminary results on pattern formation on PtBA are carried out as a function of fluence. After writing the pattern, a thin layer of Ge is deposited. Distribution of Ge in pristine and ion beam patterned surface of PtBA polymer is studied using the optical and secondary electron microscopic experimental methods.

La 2 NiMnO 6 (LNMO) was prepared by a combustion method followed by heating at high temperature. Subsequently, the preformed LNMO was annealed in air, oxygen, or N 2 atmosphere and characterized by powder x-ray diffraction (XRD), neutron diffraction, superconducting quantum interference device magnetometry, and dielectric analysis. Structural studies by XRD and neutron diffraction revealed the coexistence of partially cation disordered monoclinic (31%) and rhombohedral (69%) phases in the sample annealed in air. However, the sample annealed in oxygen shows about 50:50% of monoclinic and rhombohedral phases. Relaxor-like behavior with relative permittivity of the order of 10 4 was observed in the sample annealed in air, while relative permittivity decreases to about 200 in samples annealed in oxygen atmosphere. The magnetic properties indicate a well-defined ferromagnetic phase in the oxygen-annealed sample compared to a feeble ferromagnetic signature in the air-annealed one. The dielectric and ferromagnetism of LNMO samples have been related to formation and annihilation of oxygen vacancies.