High Flux Femtosecond X-ray Emission from the Electron-Hose Instability in Laser Wakefield Accelerators

Bright and ultrashort duration X-ray pulses can be produced by through betatron oscillations of electrons during Laser Wakefield Acceleration (LWFA). Our experimental measurements using the \textsc{Hercules} laser system demonstrate a dramatic increase in X-ray flux for interaction distances beyond the depletion/dephasing lengths, where the initial electron bunch injected into the first wake bucket catches up with the laser pulse front and the laser pulse depletes. A transition from an LWFA regime to a beam-driven plasma wakefield acceleration (PWFA) regime consequently occurs. The drive electron bunch is susceptible to the electron-hose instability and rapidly develops large amplitude oscillations in its tail, which leads to greatly enhanced X-ray radiation emission. We measure the X-ray flux as a function of acceleration length using a variable length gas cell. 3D particle-in-cell (PIC) simulations using a Monte Carlo synchrotron X-ray emission algorithm elucidate the time-dependent variations in the radiation emission processes.Comment: 6 pages, 4 figures, accepted for publication in Phys. Rev. Accel. Beam

A Combined XPS and Computational Study of the Chemical Reduction of BMP‐TFSI by Lithium

Employing density functional theory (DFT) calculations and X-ray photoelectron spectroscopy (XPS), we identify products of the reaction of the ionic liquid N,N-butylmethylpyrrolidinum bis(trifluoromethylsulfonyl)imide (BMP-TFSI) with lithium in order to model the initial chemical processes contributing to the formation of the solid electrolyte interphase in batteries. Besides lithium oxide, sulfide, carbide and fluoride, we find lithium cyanide or cyanamide as possible, thermodynamically stable product in the Li-poor regime, whilst Li$_{3}$N is the stable product in the Li-rich regime. The thermodynamically controlled reaction products as well as larger fragments of TFSI persisting due to kinetic barriers could be identified by a comparison of experimentally and computationally determined core level binding energies

Metal–organic framework derived Fe7S8 nanoparticles embedded in heteroatom-doped carbon with Lithium and Sodium storage capability

Iron sulfides are promising materials for lithium- and sodium-ion batteries owing to their high theoretical capacity and widespread abundance. Herein, the performance of an iron sulfide-carbon composite, synthesized from a Fe-based metal–organic framework (Fe-MIL-88NH2) is reported. The material is composed of ultrafine Fe7S8 nanoparticles (<10 nm in diameter) embedded in a heteroatom (N, S, and O)-doped carbonaceous framework (Fe7S8@HD-C), and is obtained via a simple and efficient one-step sulfidation process. The Fe7S8@HD-C composite, investigated in diethylene glycol dimethyl ether-based electrolytes as anode material for lithium and sodium batteries, shows high reversible capacities (930 mAh g−1 for lithium and 675 mAh g−1 for sodium at 0.1 A g−1). In situ X-ray diffraction reveals an insertion reaction to occur in the first lithiation and sodiation steps, followed by conversion reactions. The composite electrodes show rather promising long-term cycling stability and rate capability for sodium storage in glyme electrolyte, while an improved rate capacity and long-term cycling stability (800 mAh g−1 after 300 cycles at 1 A g−1) for lithium can be achieved using conventional carbonates

Potential Energy Surface for H_2 Dissociation over Pd(100)

The potential energy surface (PES) of dissociative adsorption of H_2 on Pd(100) is investigated using density functional theory and the full-potential linear augmented plane wave (FP-LAPW) method. Several dissociation pathways are identified which have a vanishing energy barrier. A pronounced dependence of the potential energy on ``cartwheel'' rotations of the molecular axis is found. The calculated PES shows no indication of the presence of a precursor state in front of the surface. Both results indicate that steering effects determine the observed decrease of the sticking coefficient at low energies of the H_2 molecules. We show that the topology of the PES is related to the dependence of the covalent H(s)-Pd(d) interactions on the orientation of the H_2 molecule.Comment: RevTeX, 8 pages, 5 figures in uufiles forma

Raising the COx Methanation Activity of a Ru/γ-Al2O3 Catalyst by Activated Modification of Metal–Support Interactions

Ru/Al2O3 is a highly stable, but less active catalyst for methanation reactions. Herein we report an effective approach to significantly improve its performance in the methanation of CO2/H2 mixtures. Highly active and stable Ru/γ-Al2O3 catalysts were prepared by high-temperature treatment in the reductive reaction gas. Operando/in situ spectroscopy and STEM imaging reveals that the strongly improved activity, by factors of 5 and 14 for CO and CO2 methanation, is accompanied by a flattening of the Ru nanoparticles and the formation of highly basic hydroxylated alumina sites. We propose a modification of the metal–support interactions (MSIs) as the origin of the increased activity, caused by modification of the Al2O3 surface in the reductive atmosphere and an increased thermal mobility of the Ru nanoparticles, allowing their transfer to modified surface sites

Differential Gene Expression at Coral Settlement and Metamorphosis - A Subtractive Hybridization Study

A successful metamorphosis from a planktonic larva to a settled polyp, which under favorable conditions will establish a future colony, is critical for the survival of corals. However, in contrast to the situation in other animals, e.g., frogs and insects, little is known about the molecular basis of coral metamorphosis. We have begun to redress this situation with previous microarray studies, but there is still a great deal to learn. In the present paper we have utilized a different technology, subtractive hybridization, to characterize genes differentially expressed across this developmental transition and to compare the success of this method to microarray.\ud \ud Methodology/Principal Findings\ud \ud Suppressive subtractive hybridization (SSH) was used to identify two pools of transcripts from the coral, Acropora millepora. One is enriched for transcripts expressed at higher levels at the pre-settlement stage, and the other for transcripts expressed at higher levels at the post-settlement stage. Virtual northern blots were used to demonstrate the efficacy of the subtractive hybridization technique. Both pools contain transcripts coding for proteins in various functional classes but transcriptional regulatory proteins were represented more frequently in the post-settlement pool. Approximately 18% of the transcripts showed no significant similarity to any other sequence on the public databases. Transcripts of particular interest were further characterized by in situ hybridization, which showed that many are regulated spatially as well as temporally. Notably, many transcripts exhibit axially restricted expression patterns that correlate with the pool from which they were isolated. Several transcripts are expressed in patterns consistent with a role in calcification.\ud \ud Conclusions\ud \ud We have characterized over 200 transcripts that are differentially expressed between the planula larva and post-settlement polyp of the coral, Acropora millepora. Sequence, putative function, and in some cases temporal and spatial expression are reported