Carbon Foils Research Articles

Underwater surface discharge characteristics and multi-physical effects with conductive coating load under fast electric pulse

Abstract Underwater pulsed discharges, where intense reactions between ionized gas and condensed-state water exist, can be a joint problem of both physics and chemistry. The study tries to build a comprehensive visualization of nanosecond-risetime discharge initiated by a conductive coating and its successive multi-physical effects. The scenario is established via a pair of thin-plate electrodes positioned on both sides of the coating, and diagnosed using high-speed backlight photography synchronized with electrical and optical measurements. For the sprayed Cu/Ag composite coating, the current density can achieve 20 A/mm2 which is high enough to induce the surface “electrical explosion” and breakup the conductive matrix within 500 ns. By increasing the discharge energy from 0.5 to 10 J, the explosion of coating can exhibit different discharge types as exploding wires. Adopting a thicker carbon foil or cermet sheet can reduce the current density and energy deposition rate, which converts the global explosion to partial ones, significantly increasing the lifetime. With the aid of the conductive coating, the breakdown delay diminishes, and hot plasma spots form in 100 ns due to non-uniform Joule heating of the pulsed current, which gradually evolve to a plasma bubble cluster above the lower-conductive coating (bypassing branch). Once the high-conductive plasma channel bridges two electrodes, it will be intensively heated (MW-level energy deposition rate) and rapidly expand, accompanied by underwater shock wave (102 kPa @30 cm) and bubble/cavity generation (20 mm maximum). Finally, microscopic characterization has been made, and the erosion morphology suggests typical arc erosion features (pits, cracks, etc.) and nanoparticles condensation from evaporated materials.

Design and initial results of the imaging neutral particle analyzer in large helical device.

A novel Imaging Neutral Particle Analyzer (INPA) was newly installed in early 2024 to enhance the understanding of fast ion confinement on Large Helical Devices (LHDs). This diagnostic system, based on a magnetic spectrometer using a scintillator, provides energy-resolved radial profiles of confined fast ions by measuring charge-exchanged fast neutrals escaping from the plasma. The system utilizes a 100nm thick carbon foil to ionize the fast neutrals, subsequently deflecting the ions toward a scintillator via the existing local magnetic field. The fast ion energy and sightline determine the position of the scintillation, while the light intensity depends on the flux of the fast ions. The INPA features two apertures, facilitating effective measurements in both clockwise and counterclockwise magnetic field directions in the LHD. This INPA was designed as a passive measurement system that measures fast ions charge exchange with background neutrals, focusing on perpendicular beam ions from 5 to 100keV with an energy resolution of about 5.75keV. This paper describes the details of the design, installation, and the initial results of the INPA on the LHD. This work will contribute significantly to a deeper understanding of fast ion transport due to magnetohydrodynamic instabilities.

Probing the interaction range of electron beam-induced etching in STEM by a non-contact electron beam

Beside its main purpose as a high-end tool in material analysis reaching the atomic scale for structure, chemical and electronic properties, aberration-corrected scanning transmission electron microscopy (STEM) is increasingly used as a tool to manipulate materials down to that very same scale. In order to obtain exact and reproducible results, it is essential to consider the interaction processes and interaction ranges between the electron beam and the involved materials. Here, we show in situ that electron beam-induced etching in a low-pressure oxygen atmosphere can extend up to a distance of several nm away from the Ångström-size electron beam, usually used for probing the sample. This relatively long-range interaction is related to beam tails and inelastic scattering involved in the etching process. To suppress the influence of surface diffusion, we measure the etching effect indirectly on isolated nm-sized holes in a 2 nm thin amorphous carbon foil that is commonly used as sample support in STEM. During our experiments, the electron beam is placed inside the nanoholes so that most electrons cannot directly participate in the etching process. We characterize the etching process from measuring etching rates at multiple nanoholes with different distances between the hole edge and the electron beam.

Improving the beam quality of the low-energy muon beamline at Paul Scherrer Institute: Characterization of ultrathin carbon foils

The low-energy muon (LEM) beamline at the Paul Scherrer Institute currently stands as the world’s only facility providing a continuous beam of low-energy muons with keV energies for conducting muon spin rotation experiments on a nanometer depth scale in heterostructures and near a sample’s surface. As such, optimizing the beam quality to reach its full potential is of paramount importance. One of the ongoing efforts is dedicated to improving the already applied technique of single muon tagging through the detection of secondary electrons emerging from an ultrathin carbon foil. In this work, we present the results from installing a thinner foil with a nominal thickness of 0.5 μg cm−2 and compare its performance to that of the previously installed foil with a nominal thickness of 2.0 μg cm−2. Our findings indicate improved beam quality, characterized by smaller beam spots, reduced energy loss and straggling of the muons, and enhanced tagging efficiency. Additionally, we introduce a method utilizing blue laser irradiation for cleaning the carbon foil, further improving and maintaining its characteristics. Published by the American Physical Society 2024

Optical probing of ultrafast laser-induced solid-to-overdense-plasma transitions

Understanding the solid target dynamics resulting from the interaction with an ultrashort laser pulse is a challenging fundamental multi-physics problem involving atomic and solid-state physics, plasma physics, and laser physics. Knowledge of the initial interplay of the underlying processes is essential to many applications ranging from low-power laser regimes like laser-induced ablation to high-power laser regimes like laser-driven ion acceleration. Accessing the properties of the so-called pre-plasma formed as the laser pulse’s rising edge ionizes the target is complicated from the theoretical and experimental point of view, and many aspects of this laser-induced transition from solid to overdense plasma over picosecond timescales are still open questions. On the one hand, laser-driven ion acceleration requires precise control of the pre-plasma because the efficiency of the acceleration process crucially depends on the target properties at the arrival of the relativistic intensity peak of the pulse. On the other hand, efficient laser ablation requires, for example, preventing the so-called “plasma shielding”. By capturing the dynamics of the initial stage of the interaction, we report on a detailed visualization of the pre-plasma formation and evolution. Nanometer-thin diamond-like carbon foils are shown to transition from solid to plasma during the laser rising edge with intensities < 1016 W/cm². Single-shot near-infrared probe transmission measurements evidence sub-picosecond dynamics of an expanding plasma with densities above 1023 cm−3 (about 100 times the critical plasma density). The complementarity of a solid-state interaction model and kinetic plasma description provides deep insight into the interplay of initial ionization, collisions, and expansion.

Probing Carbon Materials Towards the Vanadium(IV)/(V) Reaction by Scanning Electrochemical Microscopy

AbstractA method is presented to quantitatively analyze the reduction of vanadium(V) to vanadium(IV) over two flat carbon substrates (glassy carbon and graphite foil) using the feedback mode of scanning electrochemical microscopy. A pulse profile is validated and applied during approach curve experiments of a 10 μm Pt microelectrode. By fitting the approach curve data, electron transfer constants are calculated for various potentials and k0 is extracted from the corresponding Tafel plot. Furthermore, surface functional groups were introduced to the carbon substrates by acid treatment; however, kinetic parameters of the sluggish reduction reaction were only influenced to a minor extent. Finally, the same approach, combined with in situ‐Raman microscopy, is applied to a single graphene layer using a 2.7 μm Pt microelectrode. In this case, increased activity for both, the vanadium(V) reduction and vanadium(IV) oxidation reaction, was found close to the graphene edge sites by means of electrochemical microscopy for the first time.

A low-energy particle experiment for both ion and electron measurements using a single microchannel plate-based detector

We have developed a low-energy particle experiment that alternately measures ions and electrons in space. The ability to switch between ion and electron measurements is achieved by simply adding ultra-thin carbon foils and positive and negative outputs to a conventional top-hat electrostatic analyzer and a high-voltage power supply, respectively. The advantage of this experiment is that it can perform both ion and electron measurements using only one MCP-based detector for electrons, since it detects secondary electrons emitted from the carbon foils. For the SS520-3 sounding rocket program, we prepared two identical energy analyzers, one for ions and the other for electrons to demonstrate this technique. Laboratory tests confirmed that the performance of the two analyzers was comparable to that of conventional analyzers for ion and electrons. The SS520-3 rocket experiment in the high latitude auroral region yielded observations that captured typical features of ions and electrons, which were similar to previous observations.Graphical

Novel device to study double-alpha decay at the FRS Ion Catcher

A novel system has been developed to detect simultaneous double-alpha emission from purified and weightless sources. The system includes the collection of 224Ra low-energy recoils in purified helium buffer gas from the decay of 228Th. The recoil products are thermalized and collected in a cryogenic buffer gas cell and extracted into an RF-ion guide for mass selection. The mass-separated ions are implanted at low kinetic energy into a thin carbon foil placed between two large-area double-sided silicon strip detectors to observe correlated alpha-particle emission. The apparatus is described in detail, including insights into its experimental performance.

Spin-polarized 3He shock waves from a solid-gas composite target at high laser intensities

We investigate collisionless shock acceleration of spin-polarized 3 He for laser pulses with normalized vector potentials in the range a0=100−200 . The setup utilized in the 2D-particle-in-cell simulations consists of a solid carbon foil that is placed in front of the main Helium target. The foil is heated by the laser pulse and shields the Helium from the highly oscillating fields. In turn, a shock wave with more homogeneous fields is induced, leading to highly polarized ion beams. We observe that the inclusion of radiation reaction into our simulations leads to a higher beam charge without affecting the polarization degree to a significant extent.

Commissioning of the imaging neutral particle analyser for the ASDEX Upgrade tokamak

An imaging neutral particle analyser (INPA) diagnostic has been installed and commissioned at the ASDEX Upgrade (AUG) tokamak. The AUG INPA diagnostic provides energy and radially resolved measurements of the fast-ion (FI) distribution, complementing the existing set of diagnostic which measure the confined FI population. To this end, it analyses charge exchange (CX) neutrals produced in reactions between FI and neutrals injected by a neutral beam injector. These CX neutrals are ionised by a 20 nm carbon foil and deflected towards a scintillator by the machine magnetic field. The use of a scintillator as active component allows us to cover the whole plasma radial range with an energy resolution of 9 keV and a spatial of 3 cm for 93 keV deuterons. First measurements demonstrate the high sensitivity of the INPA diagnostic to different AUG fast-ion distribution functions, from NBI and ion-cyclotron resonance heating origin, and show good agreement with the synthetic diagnostic.

A conductive adhesive ink for carbon-laminated perovskite solar cells with enhanced stability and high efficiency

Utilizing carbon-laminated electrodes on perovskite solar cells (PSCs) benefits from simple fabrication process and low-cost material, in addition to enhanced stability. In this method, carbon foils are laminated on the underlying hole transport layer (HTL), so the HTL/carbon electrode interface is of the utmost importance in achieving high-performance devices. Here, we develop a conductive adhesive ink, consisting of poly methyl methacrylate (PMMA), highly conductive carbon black (HCCB), and CuInS2 (CIS) nanoparticles, as the interfacial adhesive layer between the underlying CIS HTL and the top carbon electrode. Utilizing carbon foil, wetted by the proposed optimized adhesive ink layer, allows simply pressing the top carbon electrode on CIS HTL. The prepared optimized carbon-laminated PSCs lead to a maximum power conversion efficiency (PCE) of 17.2 % for the best PSC, as compared with the maximum PCE of 18.2 % for the best sample of conventional Au-based PSC. Furthermore, the average PCE of the fabricated optimized carbon-laminated PSCs has kept almost 92 % of the average maximum PCE value after about 54 days, which is a significant enhancement in device stability in comparison with conventional Au-based PSCs, which have degraded to 75 % of their maximum PCE. The proposed carbon lamination method seems very promising for overcoming the stability challenge of PSCs, and the realization of low-cost, large-area, highly stable, and efficient solar cells.

Measurement of charge state distributions using a scintillation screen

Absolute cross sections measured using electromagnetic devices to separate and detect heavy recoiling ions need to be corrected for charge state fractions. Accurate prediction of charge state distributions using theoretical models is not always a possibility, especially in energy and mass regions where data is sparse. As such, it is often necessary to measure charge state fractions directly. In this paper we present a novel method of using a scintillation screen along with a CMOS camera to image the charge dispersed beam after a set of magnetic dipoles. A measurement of the charge state distribution for 88Sr passing through a natural carbon foil is performed. Using a Bayesian model to extract statistically meaningful uncertainties from these images, we find agreement between the new method and a more traditional method using Faraday cups. Future work is need to better understand systematic uncertainties. Our technique offers a viable method to measure charge state distributions.

The effect of flame retardants on the fire technical characteristics of recycled textiles

The paper deals with the fire technical characteristics of insulation panels made of recycled technical textiles from the automotive industry. The introductory part focuse an of the use of recycled textiles, a description and division of technical textiles, a description of the examined material and its composition, combustion processes, and the method of handling waste textiles. The monitored characteristics were the determination of the ignitability of the material, the gross calorific value as well as the radiant heat resistance. The measurements were carried out on samples from recycled technical textiles before and after their treatment with flame retardants (Isonem Anti-fire Solution, Ecogard B45, HR Prof, woven carbon foil, non-woven carbon foil). The best results in the ignitability test after treatment with liquid flame retardants were obtained after treatment with Ecogard B45. The results show that when flame retardants are used, the released heat during the combustion of the monitored materials treated through the dipping method is significantly lower from 13.7 MJ/kg to 23.7 MJ/kg. The lowest gross calorific values were achieved when using liquid flame retardant HR Prof when applied by dipping. The proportion of material that did not burn was very low (4.61 to 5.63%). After exposure to radiant heat for 10 min, the highest mass loss was 13.6% (dipping in Ecogard B45) and the smallest 1.8% (non-woven carbon foil). Based on results, it shows that flame retardant ECOGARD® B45 for the insulation material Senizol AT XX2 TL60 made from recycled technical textiles is the most suitable fire protection.

Mixed polymerization approach to GO-derived carbon foil-supported porous SiO2/C random nanocomposite films for Li-ion battery anodes with extraordinarily enhanced capacities by cycle-dependent size-reduction effect

As starting materials, tetraethyl orthosilicate, resorcinol and formaldehyde were used to prepare a distinctive composite film of SiO2/C two-phase interpenetrated porous nanostructures on the surface of carbon foil ((SiO2/C)@Cf) when the mixed polymerizations (condensations) on the surface of graphene oxide and subsequent heat treatment were carefully manipulated. The microstructures of as-prepared films were characterized by FESEM, TEM, EDS element mapping, BET, etc and their charging/discharging behaviors and electrochemical impedance spectra were quantitatively analyzed. It has been found that (SiO2/C)@Cf shows extraordinary capacity enhancement featured with excellent cycling capacity and rate performance as anode materials of Li-ion batteries, such as 1274 mAh g−1 after 2000 cycles at 1 A g−1 and 463.5 mAh g−1 at 5 A g−1, in comparison with the layered SiO2/C composite films. More interestingly, the CV curves of (SiO2/C)@Cf before and after 2000 cycles of charge/discharge evidently shows a remarkable initial pseudo-capacitive capacity and its unusual enhancement with increasing number of cycles, which should be attributed to the small size effect of SiO2 domains embedded in carbon phase and their gradual refinement, leading to an increase in the effective electrochemical reaction area and apparent diffusivity of Li-ions.

VADER: A novel decay station for actinide spectroscopy

A research programme focused on the study of the nuclear structure of actinide isotopes has recently been implemented at the IGISOL facility, University of Jyväskylä. Within this scope, a new decay station named VADER (Versatile Actinides DEcay spectRoscopy setup) has been developed and commissioned. The system consists of a compact array of silicon detectors, a liquid-nitrogen-cooled silicon lithium (Si(Li)) detector and three broad energy germanium detectors (BEGe), placed around a thin implantation carbon foil. The combined use of different detectors allows the measurement of α particles, conversion electrons and de-excitation γ rays in coincidence, enabling a full reconstruction of nuclear decay schemes. The measurement of basic nuclear decay observables provides a picture of the nuclear shell evolution in neutron-deficient actinides, and highlights the possible emergence of reflection-asymmetric shapes in the region.

Experimental benchmark data for Monte Carlo simulated radiation effects of gold nanoparticles. Part I: Experiment and raw data analysis

Electron emission spectra of gold nanoparticles (AuNPs) after photon interaction were measured over the energy range between 50 eV and 9500 eV to provide reference data for Monte Carlo radiation-transport simulations. Experiments were performed with the HAXPES spectrometer at the PETRA III high-brilliance beamline P22 at DESY (Hamburg, Germany) for photon energies below and above each of the gold L-edges, that is, at 11.9 keV, 12.0 keV, 13.7 keV, 13.8 keV, 14.3 keV, and 14.4 keV. The study focused on a sample with gold nanoparticles with an average diameter of 11.0 nm on a thin carbon foil. Additional measurements were performed on a sample with 5.3 nm gold nanoparticles and on reference samples of gold and carbon foils. Further measurements were made to calibrate the photon flux monitor, to characterize the transmission function of the electron spectrometer, and to determine the size of the photon beam. This allowed the determination of the absolute values of the spectral particle radiance of secondary electrons per incident photon flux. The paper presents the experimental and raw data analysis procedures, reviews the data obtained for the nanoparticle samples, and discusses their limitations.

On characterization of shock propagation and radiative preheating in x-ray driven high-density carbon foils

Recently, much effort has been dedicated to the high-density carbon ablator coated fuel capsule in indirect drive inertial confinement fusion experiments due to its higher density compared to other ablators. By using detailed radiation hydrodynamic simulations over a broad range of drive and target parameters, a thorough analysis is performed on shock speed, shock breakout, and maximum preheating temperature in pure and tungsten doped high density carbon foils. The ablators are irradiated by a non-equilibrium x-ray temperature drive consisting of the usual Planckian plus an additionally imposed Gaussian distribution lying in the high frequency M-band region of the incident spectrum. All variables have shown a complex interdependence on strength of the drive, its spectral distribution, and the thickness of the target. Maximum preheating temperature, an important parameter in designing experiments, reduces up to 34% for thicker high-density carbon (HDC) foils, whereas a mere 0.44% doping of tungsten in pure HDC is able to reduce preheating up to 17% for extreme drive conditions. The results are explained on the basis of variation of average albedo/wall loss behavior in foils, an outcome of the interplay between total extinction coefficient and spectral intensity variation with photon energy. For a better understanding and comparison among different types of ablators, multi-parameter scaling relations are proposed for above-mentioned variables, which govern the dynamics of shock propagation and preheating phenomena in HDC based foils.

Enhancing the chameleon grid range to unlock faster and more precise sample optimisation

The chameleon system robustly automates the process of plunge freezing and screening grids for cryo electron microscopy (cryoEM). Self-wicking grids are a key enabling technology for this blot-free, fast-plunge method. Until recently, a single type of self-wicking grids has been available for use on chameleon - R1.2/0.8 with a copper base and carbon foil. Recent research using two new self-wicking grid prototypes (“multihole” and graphene oxide support) and updates on the standard self-wicking grid range will be presented.

Chemical Imaging of Organic Materials by MeV SIMS Using a Continuous Collimated Ion Beam

MeV SIMS is a type of secondary ion mass spectrometry (SIMS) technique where molecules are desorbed from the sample surface with ions of MeV energies. In this work, we present a novel system for molecular imaging of organic materials using a continuous analytical beam and a start trigger for timing based on the detection of secondary electrons. The sample is imaged by a collimated primary ion beam and scanning of the target with a lateral resolution of ∼20 μm. The mass of the analyzed molecules is determined with a reflectron-type time-of-flight (TOF) analyzer, where the START signal for the TOF measurement is generated by the secondary electrons emitted from a thin carbon foil (∼5 nm) placed over the beam collimator. With this new configuration of the MeV SIMS setup, a primary ion beam with the highest possible electronic stopping can be used (i.e., highest secondary molecular yield), and samples of any thickness can be analyzed. Since the electrons are collected from the thin foil rather than from the sample surface, the detection efficiency of secondary electrons is always the same for any type of analyzed material. Due to the ability to scan the samples by a piezo stage, samples of a few cm in surface size can be imaged. The imaging capabilities of MeV SIMS are demonstrated on crossing ink lines deposited on paper, a thin section of a mouse brain, and a fingerprint deposited on a thick Si wafer to show the potential application of the presented technique for analytical purposes in biology and forensic science.

Method for releasing carbon foils from substrates

The performance of a carbon foil (C-foil) as a charge stripper in an accelerator is directly affected by its condition and quality. C-foils are fabricated by evaporating carbon onto a substrate. Therefore, a suitable technique must be established for depositing and removing C-foils from substrates. The selection of appropriate releasing agents is crucial for the removal process. C-foils with thicknesses less than 0.1 mg/cm2 were produced using the arc discharge method, wherein chloride materials were used as releasing agents. The magnetron sputtering method is suitable for manufacturing C-foils thicker than 0.1 mg/cm2 using appropriate releasing agents, such as fluorine-based or silicon-based agents. The contact angle analysis demonstrates a negative relationship between the C-foil thickness and the wettability of the substrate treated with an appropriate releasing agent. The possibility of using ionic liquids as novel releasing agents is also investigated.