Roland K. Schulze

Laser acceleration of quasi-monoenergetic MeV ion beams

Acceleration of particles by intense laser–plasma interactions represents a rapidly evolving field of interest, as highlighted by the recent demonstration of laser-driven relativistic beams of monoenergetic electrons. Ultrahigh-intensity lasers can produce accelerating fields of 10 TV m-1 (1 TV = 1012 V), surpassing those in conventional accelerators by six orders of magnitude. Laser-driven ions with energies of several MeV per nucleon have also been produced. Such ion beams exhibit unprecedented characteristics—short pulse lengths, high currents and low transverse emittance—but their exponential energy spectra have almost 100% energy spread. This large energy spread, which is a consequence of the experimental conditions used to date, remains the biggest impediment to the wider use of this technology. Here we report the production of quasi-monoenergetic laser-driven C5+ ions with a vastly reduced energy spread of 17%. The ions have a mean energy of 3 MeV per nucleon (full-width at half-maximum ∼0.5 MeV per nucleon) and a longitudinal emittance of less than 2 × 10-6 eV s for pulse durations shorter than 1 ps. Such laser-driven, high-current, quasi-monoenergetic ion sources may enable significant advances in the development of compact MeV ion accelerators, new diagnostics, medical physics, inertial confinement fusion and fast ignition.

Efficient hydrogen evolution in transition metal dichalcogenides via a simple one-step hydrazine reaction.

Hydrogen evolution reaction is catalysed efficiently with precious metals, such as platinum; however, transition metal dichalcogenides have recently emerged as a promising class of materials for electrocatalysis, but these materials still have low activity and durability when compared with precious metals. Here we report a simple one-step scalable approach, where MoOx/MoS2 core-shell nanowires and molybdenum disulfide sheets are exposed to dilute aqueous hydrazine at room temperature, which results in marked improvement in electrocatalytic performance. The nanowires exhibit ∼100 mV improvement in overpotential following exposure to dilute hydrazine, while also showing a 10-fold increase in current density and a significant change in Tafel slope. In situ electrical, gate-dependent measurements and spectroscopic investigations reveal that hydrazine acts as an electron dopant in molybdenum disulfide, increasing its conductivity, while also reducing the MoOx core in the core-shell nanowires, which leads to improved electrocatalytic performance.

Combined Experimental and Theoretical Investigation of the Premartensitic Transition in Ni2MnGa

Ultraviolet-photoemission (UPS) measurements and supporting specific-heat, thermal-expansion, resistivity, and magnetic-moment measurements are reported for the magnetic shape-memory alloy Ni2MnGa over the temperature range 100<T<250 K. All measurements detect clear signatures of the premartensitic transition (T(PM) approximately 247 K) and the martensitic transition (T(M) approximately 196 K). Temperature-dependent UPS shows a dramatic depletion of states (pseudogap) at T(PM) located 0.3 eV below the Fermi energy. First-principles electronic structure calculations show that the peak observed at 0.3 eV in the UPS spectra for T>T(PM) is due to the Ni d minority-spin electrons. Below T(M) this peak disappears, resulting in an enhanced density of states at energies around 0.8 eV. This enhancement reflects Ni d and Mn d electronic contributions to the majority-spin density of states.

Band Structure of SnTe Studied by Photoemission Spectroscopy

We present an angle-resolved photoemission spectroscopy study of the electronic structure of SnTe and compare the experimental results to ab initio band structure calculations as well as a simplified tight-binding model of the p bands. Our study reveals the conjectured complex Fermi surface structure near the L points showing topological changes in the bands from disconnected pockets, to open tubes, and then to cuboids as the binding energy increases, resolving lingering issues about the electronic structure. The chemical potential at the crystal surface is found to be 0.5 eV below the gap, corresponding to a carrier density of p=1.14 × 10(21)  cm(-3) or 7.2 × 10(-2) holes per unit cell. At a temperature below the cubic-rhombohedral structural transition a small shift in spectral energy of the valance band is found, in agreement with model predictions.

Epitaxial Superconducting δ-MoN Films Grown by a Chemical Solution Method

The synthesis of pure δ-MoN with desired superconducting properties usually requires extreme conditions, such as high temperature and high pressure, which hinders its fundamental studies and applications. Herein, by using a chemical solution method, epitaxial δ-MoN thin films have been grown on c-cut Al(2)O(3) substrates at a temperature lower than 900 °C and an ambient pressure. The films are phase pure and show a T(c) of 13.0 K with a sharp transition. In addition, the films show a high critical field and excellent current carrying capabilities, which further prove the superior quality of these chemically prepared epitaxial thin films.

Aqueous Pu(IV) sorption on brucite

The sorption behavior of aqueous Pu(IV) on brucite (Mg(OH)2) in the presence and absence of citrate was investigated by a combination of wet chemical batch sorption experiments and X-ray photoelectron spectroscopy (XPS). Sorption occurs rapidly at near 100% levels from pH 8 to pH 13, and is not affected by the presence of citrate. XPS results indicate that Pu was incorporated in the subsurface in the cases studied.

Initial electron backscattered diffraction observations of a plutonium alloy

Abstract In this work, the first electron backscattered diffraction patterns (EBSPs) were captured for a plutonium–gallium (Pu–Ga) alloy. The experimental techniques used for EBSP acquisition are described in detail. This demonstrated sample preparation and characterization technique is expected to be a powerful means to further understand phase transformation behavior, orientation relationships, and texture in the complicated Pu and Pu-alloy systems.

Initial electron back-scattered diffraction observations of cerium

The first electron back-scattered diffraction Kikuchi patterns and grain orientation maps were captured for pure n-phase (fcc) Ce. The sample preparation technique used for electron back-scattered diffraction orientation mapping of this surface-reactive metal included ion sputtering the surface using a scanning Auger microprobe followed by vacuum transfer of the sample from the scanning Auger microprobe to the scanning electron microscope. The effect of ion sputtering on the microstructure as well as preliminary electron back-scattered diffraction microstructural characterization is presented. Based on the sputtering data, the room-temperature diffusivity of O in n-Ce was estimated.

Electron backscatter diffraction of a plutonium–gallium alloy

Abstract An experimental technique has recently been developed to characterize reactive metals, including plutonium (Pu) and cerium, using electron backscatter diffraction (EBSD). Microstructural characterization of Pu and its alloys by EBSD had been previously elusive primarily because of the extreme toxicity and rapid surface oxidation rate associated with Pu metal. The experimental technique, which included ion-sputtering the metal surface using a scanning Auger microprobe (SAM) followed by vacuum transfer of the sample from the SAM to the scanning electron microscope (SEM), used to obtain electron backscatter diffraction Kikuchi patterns and orientation maps for a Pu–gallium alloy is described and the initial microstructural observations based on the analysis are discussed. The phase transformation behavior between the δ (face-centered cubic) and e (body-centered-cubic) structures is explained by combining the SEM and EBSD observations.

Photoelectron Spectroscopy of Plutonium at the Advanced Light Source

We are developing a program to perform Photoelectron Spectroscopy and X-Ray Absorption Spectroscopy upon highly radioactive samples, particularly Plutonium, at the Advanced Light Source in Berkeley, CA, USA. First results from alpha and delta Plutonium are reported as well as plans for a dedicated spectrometer for actinide studies.