Research of the small plasma focus with an auxiliary electrode at deuterium filling

The research was provided on the small plasma focus device with the Mather-type electrodes in configuration with an auxiliary electrode placed in front of the anode. It works at the current maximum of 200 kA. The total neutron yield from D-D reaction reaches 10⁵–10⁷ per one shot. The hard X-rays and neutrons were detected with scintillation detectors and the soft X-rays with a PIN detector and four MCP frames. We present preliminary results obtained from different configurations of the anode (inner electrode) and auxiliary electrode and we compare these results with that obtained in configuration without auxiliary electrode. The auxiliary electrode decreased both the neutron yield and the time of hard X-ray and neutron production. Different electrode faces has influence on the energy distribution of generated neutrons.     

High Energy and High Power Lithium‐Ion Capacitors Based on Boron and Nitrogen Dual‐Doped 3D Carbon Nanofibers as Both Cathode and Anode

High energy density at high power density is still a challenge for the current Li‐ion capacitors (LICs) due to the mismatch of charge‐storage capacity and electrode kinetics between capacitor‐type cathode and battery‐type anode. In this work, B and N dual‐doped 3D porous carbon nanofibers are prepared through a facile method as both capacitor‐type cathode and battery‐type anode for LICs. The B and N dual doping has profound effect in tuning the porosity, functional groups, and electrical conductivity for the porous carbon nanofibers. With rational design, the developed B and N dual‐doped carbon nanofibers (BNC) exhibit greatly improved electrochemical performance as both cathode and anode for LICs, which greatly alleviates the mismatch between the two electrodes. For the first time, a 4.5 V “dual carbon” BNC//BNC LIC device is constructed and demonstrated, exhibiting outstanding energy density and power capability compared to previously reported LICs with other configurations. In specific, the present BNC//BNC LIC device can deliver a large energy density of 220 W h kg^?1 and a high power density of 22.5 kW kg^?1 (at 104 W h kg^?1) with reasonably good cycling stability (≈81% retention after 5000 cycles).     

Generation and anisotropy of neutron emission from a condensed Z-pinch

The paper presents results of measurements of neutron emission generated in the constriction of a fast Z-pinch at the S-300 facility (2 MA, 100 ns). An increased energy concentration was achieved by using a combined load the central part of which was a microporous deuterated polyethylene neck with a mass density of 100 mg/cm³ and diameter of 1–1.5 mm. The neck was placed between two 5-mm-diameter agar-agar cylinders. The characteristics of neutron emission in two axial and two radial directions were measured by the time-of-flight method. The neutron spectrum was recovered from the measured neutron signals by the Monte Carlo method. In all experiments, the spatiotemporal characteristics of plasma in the Z-pinch constriction were measured by means of the diagnostic complex of the S-300 facility, which includes frame photography in the optical, VUV, and soft X-ray (SXR) spectral regions; optical streak imaging; SXR detection; and time-integrated SXR photography. The formation of hot dense plasma in the Z-pinch constriction was accompanied by the generation of hard X-ray (with photon energies E > 30 keV), SXR (with photon energies E > 1 keV and duration of 2–4 ns), and neutron emission. Anisotropy of the neutron energy distribution in the axial direction was revealed. The mean neutron energies measured in four directions at angles of 0° (above the anode), 90°, 180° (under the cathode), and 270° with respect to the load axis were found to be of 2.1 ± 0.1, 2.5 ± 0.1, 2.6 ± 0.2, and 2.4 ± 0.1 MeV, respectively. For a 1-mm-diameter neck, the maximum integral neutron yield was 6 × 10⁹ neutrons. The anisotropy of neutron emission for a Z-pinch with a power-law distribution of high-energy ions is calculated.     

Boosting Ion Diffusion and Charge Transfer by Zincophilic Accordion Arrays to Achieve Ultrafast Aqueous Zinc Metal Batteries

A key challenge to apply aqueous zinc metal batteries (AZMBs) as next-generation energy storage device is to improve the rechargeability at high current densities, which is needed to circumvent slowly ion diffusion in anode and sluggish charge transfer of Zn²⁺. Herein, a zincophilic accordion array derived from MOF is developed as zinc host for simultaneously boosted ion diffusion and charge transfer. The designed host is prepared by etching and disproportionation reactions, the abundant zincophilic Sn sites with nano-size uniform disperse on accordion arrays nanosheets (Sn-AA). Then a composite Zn anode (Sn-AA@Zn) is obtained by compacting Sn-AA host with zinc power (Zn-P). The Sn-AA@Zn anode has an ultra-low activation energy (37.1 kJ mol⁻¹) and nucleation overpotential (10 mV), achieving fast charge transfer of Zinc deposition. In addition, the cycle life of the symmetric cell with Sn-AA@Zn anode exceeds 13 000 cycles at 50 mA cm⁻², which is 32 times than that of the Zn-P anode. And the full cell with Sn-AA@Zn anode and MnO₂ cathode maintains a capacity of 122 mAh g⁻¹ after 5000 cycles at 5 Ag⁻¹. Hopefully, the 3D anode based on Sn-AA@Zn accordion array and Zn-P has significantly improved the rechargeability of AZMB at high current density.     

X-pinch-based neutron source

Results are presented from experimental studies of the parameters of an X-pinch-based neutron source made of 70- to 80-μm-diameter deuterated polyethylene fibers. At currents of up to 1.7 MA and a current rise time of ～150 ns, hot plasma spots were observed in the fiber crossing region. The formation of hot spots was accompanied by the generation of short soft X-ray pulses with a duration of 2–4 ns, as well as by neutron emission. The neutron energy was measured using the time-of-flight technique in four directions, at 0°, 90°, 180°, and 270° with respect to the load axis. The mean energy of the neutrons emitted along the axis towards the anode and cathode was found to be 2.0 ± 0.2 and 2.6 ± 0.1 MeV, respectively, and that of neutrons emitted in two opposite directions along the radius, 2.5 ± 0.1 and 2.4 ± 0.1 MeV. The maximum neutron yield at a current amplitude of 1.6 MA was of 10¹⁰ neutrons per shot.     

Investigating microbial fuel cell bioanode performance under different cathode conditions

A compact, three‐in‐one, flow‐through, porous, electrode design with minimal electrode spacing and minimal dead volume was implemented to develop a microbial fuel cell (MFC) with improved anode performance. A biofilm‐dominated anode consortium enriched under a multimode, continuous‐flow regime was used. The increase in the power density of the MFC was investigated by changing the cathode (type, as well as catholyte strength) to determine whether anode was limiting. The power density obtained with an air‐breathing cathode was 56 W/m³ of net anode volume (590 mW/m²) and 203 W/m³ (2160 mW/m²) with a 50‐mM ferricyanide‐based cathode. Increasing the ferricyanide concentration and ionic strength further increased the power density, reaching 304 W/m³ (3220 mW/m², with 200 mM ferricyanide and 200 mM buffer concentration). The increasing trend in the power density indicated that the anode was not limiting and that higher power densities could be obtained using cathodes capable of higher rates of oxidation. The internal solution resistance for the MFC was 5–6 Ω, which supported the improved performance of the anode design. A new parameter defined as the ratio of projected surface area to total anode volume is suggested as a design parameter to relate volumetric and area‐based power densities and to enable comparison of various MFC configurations. Published 2009 American Institute of Chemical Engineers Biotechnol. Prog., 2009     

Determination of the thermal and epithermal neutron sensitivities of an LBO chamber

An LBO (Li₂B₄O₇) walled ionization chamber was designed to monitor the epithermal neutron fluence in boron neutron capture therapy clinical irradiation. The thermal and epithermal neutron sensitivities of the device were evaluated using accelerator neutrons from the ⁹Be(d, n) reaction at a deuteron energy of 4 MeV (4 MeV d-Be neutrons). The response of the chamber in terms of the electric charge induced in the LBO chamber was compared with the thermal and epithermal neutron fluences measured using the gold-foil activation method. The thermal and epithermal neutron sensitivities obtained were expressed in units of pC cm², i.e., from the chamber response divided by neutron fluence (cm^?2). The measured LBO chamber sensitivities were 2.23 × 10^?7 ± 0.34 × 10^?7 (pC cm²) for thermal neutrons and 2.00 × 10^?5 ± 0.12 × 10^?5 (pC cm²) for epithermal neutrons. This shows that the LBO chamber is sufficiently sensitive to epithermal neutrons to be useful for epithermal neutron monitoring in BNCT irradiation.     

Quantum dots decorated photoanodes in bioelectrochemical fuel cells: Enhanced electricity generation using green algae

The power performance of the bio-electrochemical fuel cells (BEFCs) depends mainly on the energy harvesting ability of the anode material. The anode materials with low bandgap energy and high electrochemical stability are highly desirable in the BEFCs. To address this issue, a novel anode is designed using indium tin oxide (ITO) modified by chromium oxide quantum dots (CQDs). The CQDs were synthesized using facile and advanced pulsed laser ablation in liquid (PLAL) technique. The combination of ITO and CQDs improved the optical properties of the photoanode by exhibiting a broad range of absorption in the visible to UV region. A systematic study has been performed to optimize the amount of CQDs and green Algae (Alg) film grown using the drop casting method. Chlorophyll (a, b, and total) content of algal cultures (with different concentrations) were optimized to investigate the power generation performance of each cell. The BEFC cell (ITO/Alg10/Cr3//Carbon) with optimized amounts of Alg and CQDs demonstrated enhanced photocurrent generation of 120 mA cm⁻² at a photo-generated potential of 24.6 V m⁻². The same device exhibited a maximum power density of 7 W m⁻² under continuous light illumination. The device also maintained 98% of its initial performance after 30 repeated cycles of light on–off measurements.     

Graphitic Carbon Nanocage as a Stable and High Power Anode for Potassium‐Ion Batteries

As an emerging electrochemical energy storage device, potassium‐ion batteries (PIBs) have drawn growing interest due to the resource‐abundance and low cost of potassium. Graphite‐based materials, as the most common anodes for commercial Li‐ion batteries, have a very low capacity when used an anode for Na‐ion batteries, but they show reasonable capacities as anodes for PIBs. The practical application of graphitic materials in PIBs suffers from poor cyclability, however, due to the large interlayer expansion/shrinkage caused by the intercalation/deintercalation of potassium ions. Here, a highly graphitic carbon nanocage (CNC) is reported as a PIBs anode, which exhibits excellent cyclability and superior depotassiation capacity of 175 mAh g^?1 at 35 C. The potassium storage mechanism in CNC is revealed by cyclic voltammetry as due to redox reactions (intercalation/deintercalation) and double‐layer capacitance (surface adsorption/desorption). The present results give new insights into structural design for graphitic anode materials in PIBs and understanding the double‐layer capacitance effect in alkali metal ion batteries.     

Measurement of ion beam angular distribution at different helium gas pressures in a plasma focus device by large-area polycarbonate detectors

The paper presents an experimental study and analysis of full helium ion density angular distributions in a 4-kJ plasma focus device (PFD) at pressures of 10, 15, 25, and 30 mbar using large-area polycarbonate track detectors (PCTDs) (15-cm etchable diameter) processed by 50-Hz-HV electrochemical etching (ECE). Helium ion track distributions at different pressures, in particular, at the main axis of the PFD are presented. Maximum ion track density of ~4.4 × 10⁴ tracks/cm² was obtained in the PCTD placed 6 cm from the anode. The ion distributions for all pressures applied are ring-shaped, which is possibly due to the hollow cylindrical copper anode used. The large-area PCTD processed by ECE proves, at the present state-of-theart, a superior method for direct observation and analysis of ion distributions at a glance with minimum efforts and time. Some observations of the ion density distributions at different pressures are reported and discussed.     

Unintentional Bulk Doping of Polymer‐Fullerene Blends from a Thin Interfacial Layer of MoO3

Charge selective interlayers are of critical importance in order for solar cells based on low mobility materials, such as polymer‐fullerene blends, to perform well. Commonly used anode interlayers consist of high work function transition metal oxides, with molybdenum trioxide (MoO₃) being arguably the most used. Here, it is shown that a thin interlayer of MoO₃ causes unintentional bulk doping in solar cells based on polymers and polymer‐fullerene blends. The doping concentrations determined from capacitance–voltage measurements are larger than 10¹⁶ cm^?3 and are seen to increase closer to the anode, reference devices without MoO₃ are undoped. Using time of flight secondary ion mass spectroscopy it is furthermore shown that molybdenum is present on the surface of all films with an interfacial layer of MoO₃ beneath the active layer. Doping concentrations of this magnitude are detrimental for device performance, especially for active layers >100 nm.     

Strategic Pore Architecture for Accommodating Volume Change from High Si Content in Lithium‐Ion Battery Anodes

To be a thinner and more lightweight lithium‐ion battery with high energy density, the next‐generation anode with high gravimetric and volumetric capacity is a prerequisite. In this regard, utilizing high silicon (3579 mAh g^?1) content in the electrode for the anode has been highlighted as a practically relevant approach. However, there still remains a crucial issue related to intrinsic volume expansion (>300%) of silicon upon lithiation, which can directly affect severe electrode swelling as well as accelerate its capacity fading by triggering structural degradation and electrical contact loss between particles. Herein, macropore‐exploited design, which can accommodate the volume change of high silicon content within the extended pore of graphite upon repeated cycling, is introduced. Such unique macropore‐exploited design leads to much less electrode swelling, by preserving its morphological integrity and contact between particles, than that of the comparative group with different sized pore and silicon distribution. As a result, this anode (914 mAh g^?1) demonstrates notable gravimetric (220 Wh kg^?1 at 6000 W kg^?1) and volumetric energy density (623 Wh L^?1 upon full lithiation after 100 cycles), exceeding that of a nano‐silicon blended graphite anode (127 Wh kg^?1 and 229 Wh L^?1) in the full‐cell system.     

3D Vertically Aligned Li Metal Anodes with Ultrahigh Cycling Currents and Capacities of 10 mA cm−2/20 mAh cm−2 Realized by Selective Nucleation within Microchannel Walls

Although metallic lithium is regarded as the “Holy Grail” for next‐generation rechargeable batteries due to its high theoretical capacity and low overpotential, the uncontrollable Li dendrite growth, especially under high current densities and deep plating/striping, has inhibited its practical application. Herein, a 3D‐printed, vertically aligned Li anode (3DP‐VALi) is shown to efficiently guide Li deposition via a “nucleation within microchannel walls” process, enabling a high‐performance, dendrite‐free Li anode. Moreover, the microchannels within the microwalls are beneficial for promoting fast Li⁺ diffusion, supplying large space for the accommodation of Li during the plating/stripping process. The high‐surface‐area 3D anode design enables high operating current densities and high areal capacities. As a result, the Li–Li symmetric cells using 3DP‐VALi demonstrate excellent electrochemical performances as high as 10 mA cm^?2/10 mAh cm^?2 for 1500 h and 5 mA cm^?2/20 mAh cm^?2 for 400 h, respectively. Additionally, the Li–S and Li–LiFePO₄ cells using 3DP‐VALi anodes present excellent cycling stability up to 250 and 800 cycles at a rate of 1 C, respectively. It is believed that these new findings could open a new window for dendrite‐free metal anode design and pave the way toward energy storage devices with high energy/power density.     

Disordered,Large Interlayer Spacing,and Oxygen‐Rich Carbon Nanosheets for Potassium Ion Hybrid Capacitor

Potassium ion storage technology as a promising substitute for the well‐developed lithium ion storage technology is still at the infancy stage of development, and exploring suitable electrode materials is critical for its practical application. Here, the great feasibility of disordered, large interlayer spacing, and oxygen‐rich carbon nanosheets (CNSs) prepared by chemical vapor deposition for potassium ion storage applications is demonstrated. As an anode material, the CNSs exhibit outstanding rate capability as well as excellent cyclic stability. Taking advantage of this, a potassium ion hybrid capacitor (PIHC) is constructed by employing such CNSs as the battery‐type anode and activated carbon as the capacitor‐type cathode. The resulting device displays a high energy density of 149 Wh kg^?1, an ultrahigh power output of 21 kW kg^?1, as well as a long cycling life (80% capacity retention after 5000 cycles), which are all close to the state‐of‐the‐art values for PIHCs. This work promotes the development of high‐performance anode material for potassium ion storage devices, and the designed PIHC pushes the energy density and power density to a higher level.     

Development and study of a portable plasma focus neutron source

The work is devoted to designing a compact pulsed neutron source on the basis of a plasma focus (PF) discharge. The main task was to study the physical processes accompanying a sub-kilojoule repetitive PF discharge. A device with a power supply energy of up to 600 J and pulse repetition rate of up to 10 Hz has been developed and put into operation. The dependence of the neutron yield as a function of the pulse repetition rate has been studied experimentally. A neutron flux of ～10⁸ neutrons/s has been obtained in the 3-s-long packet mode with a repetition rate of 10 Hz and discharge current of 80–90 kA.     

Formation of hot spots in the plasma of a Z-pinch produced from low-density deuterated polyethylene

Results are presented from experimental studies of the plasma formation dynamics in a Z-pinch produced from a cylindrical microporous agar-agar load. The experiments were performed on the S-300 facility at a current of 2 MA and current rise time of 100 ns. To enhance the energy concentration, a deuterated polyethylene neck with a mass density of 50–75 μg/cm³ and diameter of 1–2 mm was made in the central part of the load. The spatiotemporal characteristics of the Z-pinch were studied using an optical streak camera and fast frame photography in the optical and soft X-ray spectral ranges. X-ray emission was detected using semiconductor and vacuum diodes, and neutron emission was studied by means of the time-of-flight method. It is found that, in the course of continuous plasma production, hot spots with a diameter of 100 μm form in the pinch plasma. The hot spots emit short soft X-ray pulses with a duration of 2–4 ns, as well as neutron pulses with an average neutron energy of about 2.45 MeV. The maximum neutron yield was found to be 4.5 × 10⁹ neutrons per shot. The scenario of hot spot formation is adequately described by two-dimensional MHD simulations.     

Heteroatom‐Doped Mesoporous Hollow Carbon Spheres for Fast Sodium Storage with an Ultralong Cycle Life

Carbon materials have attracted significant attention as anode materials for sodium ion batteries (SIBs). Developing a carbon anode with long‐term cycling stability under ultrahigh rate is essential for practical application of SIBs in energy storage systems. Herein, sulfur and nitrogen codoped mesoporous hollow carbon spheres are developed, exhibiting high rate performance of 144 mA h g^?1 at 20 A g^?1, and excellent cycling durability under ultrahigh current density. Interestingly, during 7000 cycles at a current density of 20 A g^?1, the capacity of the electrode gradually increases to 180 mA h g^?1. The mechanisms for the superior electrochemical performance and capacity improvement of the cells are studied by electrochemical tests, ex situ transmission electron microscopy, X‐ray diffraction, X‐ray photoelectron spectroscopy, and Raman analysis of fresh and cycled electrodes. The unique and robust structure of the material can enhance transport kinetics of electrons and sodium ions, and maintain fast sodium storage from the capacitive process under high rate. The self‐rearrangement of the carbon structure, induced by continuous discharge and charge, lead to the capacity improvement with cycles. These results demonstrate a new avenue to design advanced anode materials for SIBs.     

Correlation between the neutron yield from a plasma focus device and the jump in the discharge current

The correlation between the neutron yield Y from a plasma focus device and the jump in the discharge current ??I has been studied experimentally. The total yield of the DD neutron source was measured by the method of activation of silver isotopes. The time dependences of the neutron and ??-radiation yields were recorded using scintillation detectors. It is found that, for the given experimental device, the neutron yield depends linearly on the jump in the discharge current ??I at the instant of neutron generation. The influence of the initial deuterium pressure in the discharge chamber on this dependence is examined.     

Neutron and X-ray Crystal Structures of a Perdeuterated Enzyme Inhibitor Complex Reveal the Catalytic Proton Network of the Toho-1 β-Lactamase for the Acylation Reaction

The mechanism by which class A β-lactamases hydrolyze β-lactam antibiotics has been the subject of intensive investigation using many different experimental techniques. Here, we report on the novel use of both neutron and high resolution x-ray diffraction to help elucidate the identity of the catalytic base in the acylation part of the catalytic cycle, wherein the β-lactam ring is opened and an acyl-enzyme intermediate forms. To generate protein crystals optimized for neutron diffraction, we produced a perdeuterated form of the Toho-1 β-lactamase R274N/R276N mutant. Protein perdeuteration, which involves replacing all of the hydrogen atoms in a protein with deuterium, gives a much stronger signal in neutron diffraction and enables the positions of individual deuterium atoms to be located. We also synthesized a perdeuterated acylation transition state analog, benzothiophene-2-boronic acid, which was also isotopically enriched with ¹¹B, as ¹⁰B is a known neutron absorber. Using the neutron diffraction data from the perdeuterated enzyme-inhibitor complex, we were able to determine the positions of deuterium atoms in the active site directly rather than by inference. The neutron diffraction results, along with supporting bond-length analysis from high resolution x-ray diffraction, strongly suggest that Glu-166 acts as the general base during the acylation reaction.     

A 13C(d,n)-based epithermal neutron source for Boron Neutron Capture Therapy

PurposeBoron Neutron Capture Therapy (BNCT) requires neutron sources suitable for in-hospital siting. Low-energy particle accelerators working in conjunction with a neutron producing reaction are the most appropriate choice for this purpose. One of the possible nuclear reactions is ¹³C(d,n)¹⁴N. The aim of this work is to evaluate the therapeutic capabilities of the neutron beam produced by this reaction, through a 30 mA beam of deuterons of 1.45 MeV.MethodsA Beam Shaping Assembly design was computationally optimized. Depth dose profiles in a Snyder head phantom were simulated with the MCNP code for a number of BSA configurations. In order to optimize the treatment capabilities, the BSA configuration was determined as the one that allows maximizing both the tumor dose and the penetration depth while keeping doses to healthy tissues under the tolerance limits.ResultsSignificant doses to tumor tissues were achieved up to ∼6 cm in depth. Peak doses up to 57 Gy-Eq can be delivered in a fractionated scheme of 2 irradiations of approximately 1 h each. In a single 1 h irradiation, lower but still acceptable doses to tumor are also feasible.ConclusionsTreatment capabilities obtained here are comparable to those achieved with other accelerator-based neutron sources, making of the ¹³C(d,n)¹⁴N reaction a realistic option for producing therapeutic neutron beams through a low-energy particle accelerator.