Plasma opening switch for the MOL generator

Problems related to creating a superpower pulsed current generator (Baikal project, ≈10 MV, ≈50 MA, ≈150 ns) for inertial confinement fusion are considered. In order to test the circuit design of the generator, the MOL unit (3.7 MA, 5 MV, 150 ns), in which a plasma opening switch (POS) is proposed for use as an output power sharpener, is now under construction. Results are presented from experimental testing of a number of proposals enabling the POS operation under the MOL conditions: (i) plasma guns were employed to connect the POS to the inductive storage circuit, (ii) a separating discharger was used to avoid a POS reclosure and to switch the current to a load whose impedance was initially low and increased with time, and (iii) a programmable filling of the POS gap with plasma was implemented in order for the POS to pass a long current prepulse with parameters close to those in actual systems.     

Synchronization of parallel-connected plasma opening switches and switching the current to the load

The possibility of using plasma opening switches (POSs) to create superpower generators is considered. To decrease the linear density of the charge passed through a POS of reasonable size, it is proposed to use a compact multimodule POS system. The design of an individual POS module is presented. The compact arrangement of the modules is ensured by an external magnetic field. It is proposed to use a sharpening spark gap to increase the efficiency of a multimodule POS operating with a low-inductance load. The results are presented of experiments on synchronizing two POS modules and switching the current to a low-inductance load.     

Influence of the electrode system on the emission characteristics of a vacuum spark

The influence of the electrode system on the emission characteristics of a high-current low-inductance vacuum spark is investigated. It is shown that the structure and composition of the spark plasma radiating in the X-ray spectral range depend substantially on the geometry and relative position of the electrodes. A mechanism related to the effect of the initial distribution of the electric field in the electrode gap is proposed to explain such a dependence. The conditions in which the radiating plasma forms from the erosion products of one or both electrodes are determined.     

Specific features of radiation from a negative air corona operating in the Trichel-pulse mode

Experimental studies of spatiotemporal characteristics of radiation from a negative corona operating in the Trichel-pulse mode in the point-to-sphere electrode geometry have revealed two emission zones. In addition to the well-known glow near the point electrode, there is also an anode glow, whose intensity depends substantially on the shape of the anode. It is found that the anode glow is delayed with respect to the beginning of the Trichel pulse by a time that depends on the gap length and gap voltage. The emission spectrum of the anode glow in the wavelength range 300–400 nm is identified as the spectrum of the second positive system of nitrogen (the C ³Π _u -B ³Π _g transition).     

Some features of horizontally oriented low-current electric arc in air

The properties of an electric arc operating in open air at currents of lower than 1 A were studied experimentally. The rod cathode was oriented horizontally. Cylindrical rods and plane plates either installed strictly vertically in front of the cathode end or tilted at a certain angle served as the anode. It is shown that, with such an electrode configuration, it is possible to form a discharge channel much longer than the electrode gap length. Regimes of regular oscillations are revealed, and conditions for their appearance are established. The electric field strength in the arc column and the electron temperature near the anode are calculated.     

A Portable and Efficient Solar‐Rechargeable Battery with Ultrafast Photo‐Charge/Discharge Rate

The solar‐rechargeable electric energy storage systems (SEESSs), which can simultaneously harvest and store solar energy, are considered a promising next‐generation renewable energy supply system. However, the difficulty in meeting the demands of higher overall photoelectric conversion and storage efficiency (PCSE) with both high power density and large energy density in the current SEESSs severely limit their practical application. Herein, a new class is demonstrated of portable and highly efficient SEESS that uniquely integrates a perovskite solar module (PSM) and an aluminum‐ion battery (AIB) directly on a bifunctional aluminum electrode without any external circuit. Such nanostructural design in the SEESS not only exhibits fast photo‐charge/discharge rate (less than one minute) with high power density (above 5000 W kg^?1), but also delivers a high energy density (above 43 Wh kg^?1). By rationally matching the maximum power point voltage of PSM with AIB charging voltage, an excellent solar‐charging efficiency of 15.2% and a high PCSE of 12.04% are achieved, which is among the best in all reported portable SEESSs. Moreover, enhanced PCSE is observed as the light intensity decreases, which makes such SEESS immune from the geographical location and climate limitations for diverse practical applications.     

Limiting Parameters of the Plasma Opening Switch

Implementing programs for nuclear fusion research and X-ray generation requires the creation of superpower generators based on plasma opening switches (POSs) capable of commutating currents as high as several tens of megaamperes at output voltages of up to 5 MV and higher. The physical mechanisms limiting the POS voltage are investigated. It is shown that, as the generator voltage U _g increases, the voltage multiplication factor k = U_POS/U_g (where U_POS is the POS voltage) decreases. An explanation for such a dependence is proposed, and the maximum value of the POS voltage is estimated. A POS design that enables operating in the above current and voltage ranges is considered. The design is based on applying an external magnetic field to the POS interelectrode gap, increasing the initial generator voltage, and decreasing the linear (along the perimeter of the outer electrode) density of the charge passing through the POS during the conduction phase.     

Calculation of the field and current density distributions in a non-self-sustained discharge in the discharge chamber of a CO laser

Two-dimensional spatial distributions of the electric field and current density in a non-self-sustained discharge controlled by a fast electron beam were calculated in the quasineutral plasma approximation. The calculations were carried out for a gas-discharge chamber with an antistreamer electrode grid placed in parallel to the output window of the ionizer. The voltage drop near the grid surface that appears due to the inhomogeneity of the spatial distribution of the current density was calculated. The fraction of the discharge current that passes the grid and flows onto the foil separating the vacuum volume of the ionizer from the gas-discharge chamber was estimated. The dependence of the calculated values on the geometric parameters of the electrode grid and its position with respect to the output of the ionizer was analyzed.     

Dynamics of the plasma injected into the gap of a plasma opening switch across a strong magnetic field

A method is proposed to increase the linear charge density transferred through a plasma opening switch (POS) and, accordingly, reduce the POS diameter by enhancing the external magnetic field in the POS gap. Results are presented from experimental studies of the dynamics of the plasma injected into the POS gap across a strong magnetic field. The possibility of closing the POS gap by the plasma injected across an external magnetic field of up to 60 kG is demonstrated.     

Lithium Ion Capacitors in Organic Electrolyte System: Scientific Problems,Material Development,and Key Technologies

Lithium ion capacitors (LICs), which are hybrid electrochemical energy storage devices combining the intercalation/deintercalation mechanism of a lithium‐ion battery (LIB) electrode with the adsorption/desorption mechanism of an electric double‐layer capacitor (EDLC) electrode, have been extensively investigated during the past few years by virtue of their high energy density, rapid power output, and excellent cycleability. In this review, the LICs are defined as the devices with an electrochemical intercalation electrode and a capacitive electrode in organic electrolytes. Both electrodes can serve as anode or cathode. Throughout the history of LICs, tremendous efforts have been devoted to design suitable electrode materials or develop novel type LIC systems. However, one of the key challenges encountered by LICs is how to balance the sluggish kinetics of intercalation electrodes with high specific capacity against the high power characteristics of capacitive electrode with low specific capacitance. Herein, the developments and the latest advances of LIC in material design strategies and key techniques according to the basic scientific problems are summarized. Perspectives for further development of LICs toward practical applications are also proposed.     

Experimental Study of Heating of a Liquid Cathode and Transfer of Its Components into the Gas Phase under the Action of a DC Discharge

An atmospheric-pressure dc discharge in air (i = 10–50 mA) with metal and liquid electrolyte electrodes was studied experimentally. An aqueous solution of sodium chloride (0.5 mol/L) was used as the cathode or anode. The electric field strength in the plasma and the cathode (anode) voltage drops were obtained from the measured dependences of the discharge voltage on the electrode gap length. The gas temperature was deduced from the spectral distribution of nitrogen emission in the band N₂(C³Π _u → B³Π _g , 0–2). The time dependences of the temperatures of the liquid electrolyte electrodes during the discharge and in its afterglow, as well as the evaporation rate of the solution, were determined experimentally. The contributions of ion bombardment and heat flux from the plasma to the heating of the liquid electrode and transfer of solvent (water) into the gas phase are discussed using the experimental data obtained.     

Dynamics of the spatial structure of pulsed discharges in dense gases in point cathode−plane anode gaps and their erosion effect on the plane electrode surface

The dynamics of the spatial structure of the plasma of pulsed discharges in air and nitrogen in a nonuniform electric field and their erosion effect on the plane anode surface were studied experimentally. It is established that, at a nanosecond front of the voltage pulse, a diffuse discharge forms in the point cathode–plane anode gap due to the ionization wave propagating from the cathode. As the gap length decreases, the diffuse discharge transforms into a spark. A bright spot on the anode appears during the diffuse discharge, while the spark channel forms in the later discharge stage. The microstructure of autographs of anode spots and spark channels in discharges with durations of several nanoseconds is revealed. The autographs consist of up to 100 and more microcraters 5–100 μm in diameter. It is shown that, due to the short duration of the voltage pulse, a diffuse discharge can be implemented, several pulses of which do not produce appreciable erosion on the plane anode or the soot coating deposited on it.     

Probing and Mapping Electrode Surfaces in Solid Oxide Fuel Cells

Solid oxide fuel cells (SOFCs) are potentially the most efficient and cost-effective solution to utilization of a wide variety of fuels beyond hydrogen ^1-7. The performance of SOFCs and the rates of many chemical and energy transformation processes in energy storage and conversion devices in general are limited primarily by charge and mass transfer along electrode surfaces and across interfaces. Unfortunately, the mechanistic understanding of these processes is still lacking, due largely to the difficulty of characterizing these processes under in situ conditions. This knowledge gap is a chief obstacle to SOFC commercialization. The development of tools for probing and mapping surface chemistries relevant to electrode reactions is vital to unraveling the mechanisms of surface processes and to achieving rational design of new electrode materials for more efficient energy storage and conversion². Among the relatively few in situ surface analysis methods, Raman spectroscopy can be performed even with high temperatures and harsh atmospheres, making it ideal for characterizing chemical processes relevant to SOFC anode performance and degradation^8-12. It can also be used alongside electrochemical measurements, potentially allowing direct correlation of electrochemistry to surface chemistry in an operating cell. Proper in situ Raman mapping measurements would be useful for pin-pointing important anode reaction mechanisms because of its sensitivity to the relevant species, including anode performance degradation through carbon deposition^{8, 10, 13, 14} ("coking") and sulfur poisoning^{11, 15} and the manner in which surface modifications stave off this degradation¹⁶. The current work demonstrates significant progress towards this capability. In addition, the family of scanning probe microscopy (SPM) techniques provides a special approach to interrogate the electrode surface with nanoscale resolution. Besides the surface topography that is routinely collected by AFM and STM, other properties such as local electronic states, ion diffusion coefficient and surface potential can also be investigated^17-22. In this work, electrochemical measurements, Raman spectroscopy, and SPM were used in conjunction with a novel test electrode platform that consists of a Ni mesh electrode embedded in an yttria-stabilized zirconia (YSZ) electrolyte. Cell performance testing and impedance spectroscopy under fuel containing H₂S was characterized, and Raman mapping was used to further elucidate the nature of sulfur poisoning. In situ Raman monitoring was used to investigate coking behavior. Finally, atomic force microscopy (AFM) and electrostatic force microscopy (EFM) were used to further visualize carbon deposition on the nanoscale. From this research, we desire to produce a more complete picture of the SOFC anode.     

A Desolvated Solid–Solid Interface for a High‐Capacitance Electric Double Layer

Understanding the electric double layer is essential for achieving efficient electrochemical energy storage technologies. A conventional solid–liquid electrode interface suffers from serious self‐discharge and a narrow voltage window, which makes the development of a solid–solid interface imperative. However, an in‐depth understanding of the electric double layer with a solid–solid interface is lacking. Here, a solid–solid interfacial electric double layer is proposed with excellent electrochemical performance. The solid layer is constructed by the electrochemical decomposition of lithium difluoro(oxalate)borate, which provides a desolvated environment for the establishment of a electric double layer. This makes a stronger interaction between the electrode surface and the ions. Based on this unique property, it is found that the solid–solid interfacial electric double layer has an increased capacitance, which suggests a way to develop high‐energy electrochemical capacitors.     

Electric field induced desorption of bacteria from a conditioning film covered substratum.

Desorption of three oral bacterial strains from a salivary conditioning film on an indium tin oxide electrode during application of a positive (bacterial adhesion to the anode) or a negative electric current was studied in a parallel plate flow chamber. Bacterial adhesion was from a flowing suspension of high ionic strength, after which the bacterial suspension was replaced by a low ionic strength solution without bacteria and currents ranging from -800 to +800 microA were applied. Streptococcus oralis J22 desorbed during application of a positive and negative electric current with a desorption probability that increased with increasing electric current. Two actinomyces strains, however, could not be stimulated to desorb by the electric currents applied. The desorption forces acting on adhering bacteria are electroosmotic in origin and working parallel to the electrode surface in case of a positive current, whereas they are electrophoretic and electrostatic in origin and working perpendicular to the surface in case of a negative current. By comparison of the effect of positive and negative electric currents, it can be concluded that parallel forces are more effective in stimulating bacterial desorption than perpendicular forces. The results of this study point to a new pathway of cleaning industrial and biomedical surfaces without the use of detergents or biocides.     

Role of the protein's low dielectric constant in the functioning of the photosynthetic reaction center

The high efficiency of the energy storage in the photosynthetic reaction center (RC) is determined by a successful competition of electron transfer from bacteriopheophytin to quinone, as compared to backward recombination of the primary charge-separated state. This relationship is caused by a fine matching of the reorganization energy and the free energy gap making the forward processes activationless, and hence very fast, and mismatching of these two quantities for the backreaction, therefore retarding it strongly. In this study, we show that this matching is due to a low dielectric constant of the RC's protein core because a low dielectric affects strongly electrostatic polarization components of both the reorganization energy and the equilibrium free energy of reaction. If the protein and membrane were replaced by a homogeneous medium with a high dielectric constant, the effective energy storage would be impractical.     

Advanced Phosphorus‐Based Materials for Lithium/Sodium‐Ion Batteries: Recent Developments and Future Perspectives

High‐performance and lost‐cost lithium‐ion and sodium‐ion batteries are highly desirable for a wide range of applications including portable electronic devices, transportation (e.g., electric vehicles, hybrid vehicles, etc.), and renewable energy storage systems. Great research efforts have been devoted to developing alternative anode materials with superior electrochemical properties since the anode materials used are closely related to the capacity and safety characteristics of the batteries. With the theoretical capacity of 2596 mA h g^?1, phosphorus is considered to be the highest capacity anode material for sodium‐ion batteries and one of the most attractive anode materials for lithium‐ion batteries. This work provides a comprehensive study on the most recent advancements in the rational design of phosphorus‐based anode materials for both lithium‐ion and sodium‐ion batteries. The currently available approaches to phosphorus‐based composites along with their merits and challenges are summarized and discussed. Furthermore, some present underpinning issues and future prospects for the further development of advanced phosphorus‐based materials for energy storage/conversion systems are discussed.     

Boosting Sodium Storage in TiF3/Carbon Core/Sheath Nanofibers through an Efficient Mixed‐Conducting Network

Sodium‐ion batteries (SIBs) are considered to be promising energy storage devices for large‐scale grid storage application due to the vast earth‐abundance and low cost of sodium‐containing precursors. Designing and fabricating a highly efficient anode is one of the keys to improve the electrochemical performance of SIBs. Recently, fluoride‐based materials are found to show an exceptional anode function with high theoretical specific capacity, based on open‐framework structure enabling Na insertion and also exhibiting improved safety. However, fluoride‐based materials suffer from sluggish kinetics and poor capacity retention essentially due to low electric conductivity. Here, an efficient mixed‐conducting network offering fast pathways is proposed to address these issues. This network relies on titanium fluoride?carbon (TiF₃?C) core/sheath nanofibers that are prepared via electrospinning. Such highly interconnected electrodes exhibit an enhanced and faster sodium storage performance. Carbon sheath nanofibers are key to an efficient ion‐ and electron‐conducting network that enable Na⁺/e^? transfer to reach the nanosized TiF₃. In addition, in‐situ‐converted Ti and NaF particles embedded in the carbon matrix allow high reversible interfacial storage. As a result, the TiF₃?C core/sheath electrode exhibits a high capacity of 161 mAh g^?1 at a high current density of 1000 mA g^?1 over 2000 cycles.     

Peculiarities of an electric discharge between an electrolytic cathode and a metal anode

Results from experimental studies of an electric discharge operating between a solid anode and an electrolytic cathode in a wide pressure range are presented. Specific features of the discharge ignition and discharge shape and peculiarities the structure of cathode spots on the electrolyte surface and anode spots on the surface of the solid electrode are revealed. The dependences of the current density on the electrolytic cathode and metal anode on the total current are measured, and the spatial distribution of the electric field is determined. A transition of a glow discharge into a multichannel discharge is investigated. The experimental data on the frequency and amplitude of the current and voltage pulsations are presented. Requirements for the maintenance of an electric discharge with an electrolytic cathode are formulated using the obtained experimental results.     

Nanosecond pulsed electric field generators for the study of subcellular effects

Modeling and experimental studies have shown that pulsed electric fields of nanosecond duration and megavolt per meter amplitude affect subcellular structures but do not lead to the formation of large pores in the outer membrane. This "intracellular electromanipulation" requires the use of pulse generators which provide extremely high power but low energy pulses. In this study, we describe the concept of the required pulsed power sources, their design, operation, and the necessary diagnostics. Two types of pulse generators based on the Blumlein line principle have been developed and are described here. One system is designed to treat a large number of cells in cuvettes holding volumes from 0.1 to 0.8 ml. Pulses of up to 40 kV amplitude, with a duration of 10 ns and a rise time close to 1 ns can be applied to the cuvette. For an electrode gap of 1 mm this voltage corresponds to an average electric field of 40 MV/m. The second system allows for real time observation of individual cells under a microscope. It generates pulses of 10-300 ns duration with a rise time of 3.5 ns and voltage amplitudes up to 1 kV. Connected to a microreactor with an electrode gap of 100 microm, electric fields up to 10 MV/m are applied.