Generation Research Articles

Scattering of Superthermal Ions at Shocks: Dependence on Energy

Diffusive shock acceleration requires the production of backstreaming superthermal ions (injection) as a first step. Such ions can be generated in the process of scattering of ions in the superthermal tail off the shock front. Knowledge of the scattering of high-energy ions is essential for matching conditions of upstream and downstream distributions at the shock transition. Here we analyze the generation of backstreaming ions as a function of their initial energy in a model stationary shock and in a similar rippled shock. Rippling substantially enhances ion reflection and the generation of backstreaming ions for slightly and moderately superthermal energies, and thus is capable of ensuring ion injection into a further diffusive shock acceleration process. For high-energy ions, there is almost no difference in the fraction of backstreaming ions produced and the ion distributions between the planar stationary shock and the rippled shock.

Diagnostic utility of N-terminal TMPP labels for unambiguous identification of clipped sites in therapeutic proteins

Protein therapeutics are susceptible to clipping via enzymatic and nonenzymatic mechanisms that create neo-N-termini. Typically, neo-N-termini are identified by chemical derivatization of the N-terminal amine with (N-Succinimidyloxycarbonylmethyl)tris(2,4,6-trimethoxyphenyl)phosphonium bromide (TMPP) followed by proteolysis and mass spectrometric analysis. Detection of the TMPP-labeled peptide is achieved by mapping the peptide sequence to the product ion spectrum derived from collisional activation. The site-specific localization of the TMPP tag enables unambiguous determination of the true N-terminus or neo-N-termini. In addition to backbone product ions, TMPP reporter ions at m/z 573, formed via collision-induced dissociation, can be diagnostic for the presence of a processed N-termini. However, reporter ions generated by collision-induced dissociation may be uninformative because of their low abundance. We demonstrate a novel high-throughput LC–MS method for the facile generation of the TMPP reporter ion at m/z 533 and, in some instances m/z 590, upon electron transfer dissociation. We further demonstrate the diagnostic utility of TMPP labeled peptides derived from a total cell lysate shows high degree of specificity towards selective N-terminal labeling over labeling of lysine and tyrosine and highly-diagnostic Receiver Operating Characteristic’s (ROC) of TMPP reporter ions of m/z 533 and m/z 590. The abundant generation of these reporters enables subsequent MS/MS by intensity and m/z-dependent triggering of complementary ion activation modes such as collision-induced dissociation, high-energy collision dissociation, or ultraviolet photo dissociation for subsequent peptide sequencing.

Photoelectrochemical advanced oxidation processes for simultaneous removal of antibiotics and heavy metal ions in wastewater using 2D-on-2D WS2@CoFe2O4 heteronanostructures

The presence of antibiotics in water poses significant threats to both human health and the environment. Addressing this issue requires the effective treatment of medical wastewater. Photoelectrochemical advanced oxidation processes (PEAOPs) are emerging as promising solutions for wastewater treatment. This process utilizes photocatalysts to convert charge carriers into reactive species such as hydroxyl radicals and superoxide ions, which are essential for degrading pollutants in wastewater. However, limitations in charge carrier separation and transport have hindered the efficiency of photoelectrochemical advanced oxidation processes. To overcome these limitations, we designed WS2@CoFe2O4 heterojunctions, optimizing their energy levels to enhance charge transport and separation. This improvement significantly increased the oxidation of antibiotics such as amoxicillin and azithromycin. Multiple reactions occurred at the WS2@CoFe2O4 heterojunctions during photoelectrochemical advanced oxidation processes, leading to the impressive degradation of up to 99% of antibiotics under visible light irradiation at 0.8 V. Urea and H2O2 acted as oxidation agents within photoelectrochemical advanced oxidation processes, amplifying the generation of hydroxyl radicals and superoxide ions, further enhancing antibiotic oxidation. Moreover, the WS2@CoFe2O4 photoanode efficiently oxidized toxic antibiotics while converting As(III) into the less harmful As(V). Crucially, recyclability tests confirmed the robustness of the WS2@CoFe2O4 photoanode, ensuring its suitability for prolonged use in photoelectrochemical advanced oxidation processes. Integrating WS2@CoFe2O4 photoanodes into water purification systems can enhance efficiency, reduce energy consumption, and improve economic viability. This technology's scalability and its ability to protect ecosystems while conserving water resources make it a promising solution for addressing the critical issue of antibiotic pollution in water environments.

High-Energy Ion Generation During Difference-Frequency ICRF Wave Heating in GAMMA 10/PDX

High-Energy Ion Generation During Difference-Frequency ICRF Wave Heating in GAMMA 10/PDX

A ROS reservoir based on a polyoxometalate and metal-organic framework hybrid for efficient bacteria eradication and wound healing

Infections by bacteria always post significant challenges to global human health. Recent developed non-antibiotic treatment, such as using metal–organic frameworks (MOFs) to kill bacteria by generating reactive oxygen species (ROS) represents a promising strategy. However, drawbacks including low efficiencies of ROS generation and high concentrations of toxic metal ions released always exist. We have creatively designed a robust polyoxometalate (POM) and MOF hybrid (denoted as CuPOM-MOF@S) that functions as an efficient catalytic reservoir for cascaded generation of ROS (mainly ·OH) from H2O2 thus eradicating bacteria and enhancing wound healing at an administration dosage as low as 5 μg∙mL−1. The remarkable antibacterial capability surpasses those for most MOF-based materials reported thus far, which is mainly attributed to the reservation of massive catalytic copper ions, the synergistic effect regarding catalytic activity between MOFs and Keggin-type POMs as well as its bacteria-capturing ability by the coated surfactants. Its biological safety is investigated and confirmed by cell cytotoxicity and body weight assessment. This work presents a prospective strategy towards cascaded ROS generation by combining inorganic catalytic POMs with MOFs thus for multiple biomedical applications including treating bacterial infections and cancer as well as inducing biological signal responses.

Hydrochemical characteristics and the impact of human activities on groundwater in a semi-arid plain: a case study of western Jilin Province, Northeast China.

Groundwater is important for human survival and development, particularly in arid and semi-arid regions. This study aimed to analyze the hydrochemical characteristics, influencing factors, and the impact of human activities on groundwater in the semi-arid plains of western Jilin Province, northwest China. The study collected 88 and 151 phreatic and confined water samples, respectively, which were analyzed for 13 water quality indicators using statistical and graphical methods. In order to investigate the impact of anthropogenic activities on water quality and health risks, the improved combined weighted water quality index (ICWQI) based on the entropy weight, criteria importance though inter-criteria correlation (CRITIC), the coefficient of difference method, subjective weight based on quality grading criteria, and the water quality index (WQI) were proposed to evaluate the water quality of the study area. Meanwhile, the human health risk assessment (HHRA) model was used to assess the risks of nitrate to the health of humans in different ages and sex categories. The results indicated that the groundwater in the study area was weakly alkaline and the main hydrochemical types in the phreatic and confined water were HCO3-·Ca-Mg and HCO3--Na. Rock weathering was the dominant process responsible for the generation of groundwater ions, the ions in groundwater primarily originate from the dissolution of halite, gypsum, and feldspar, while dolomitization promotes an increase in Mg2+. Human activities lead to an increase in NO3- in groundwater and have an impact on water quality and human health risks. The ICWQI method was found to yield more precise and rational assessments of water quality. Groundwater quality is primarily affected by nitrate ions. The areas in which groundwater nitrate posed a higher risk to human health were found to be mainly in the saline-alkali lands of Qian'an, Tongyu, and Zhenlai. Fertilizers, pesticides, and livestock farming activities contribute to the pollution of surface water. This surface contamination then infiltrates abandoned confined wells, leading to contamination of the confined aquifers. This study can improve the understanding of groundwater hydrochemical characteristics and the impact of human activities on groundwater in the study area. This study can also contribute to the study of groundwater in semi-arid regions.

Direct Air Capture: Effects of Low-Purity CO2 and Geological Depths on Post-Capture Compression Energy and Storage

Phreeqc software has been successfully employed to study the behaviour of the gypsum rock-water system under different conditions and various levels of impurities present in the injected CO2 stream. The dissolution of gypsum leads to the increase in water quantity because of release of hydration water molecules. Under the conditions at 1km geological depth, an anhydrite (CaSO4) produced remained dissolved in the solution while the pH slightly drops owing to sulphate ions generation. As the pressure and temperature increase at 1.5km depth, more gypsum dissolves until at 2.5km depth where excess rise in temperature inhibits gypsum dissolution. The injection of pure CO2 leads to the production of calcite in the solution, which continues to grow as more CO2 is injected. But, the presence of impurity such as N2 in the CO2 stream inhibits formation of calcite, owing to continuous dissolution/ionization of calcium. Other carbonate crystals were similarly affected while the pH continues to drop drastically. It is inferred that the presence of impurities such as N2 in the CO2 stream complicates carbonation mechanisms and inhibits formations of the carbonate crystals.

Analysis of a UV photocatalytic oxidation-based disinfection system for hydroxyl radicals, negative air ions generation and their impact on inactivation of pathogenic micro-organisms.

This work presents a large-scale surface disinfection system, which has a unique lantern arrangement of ultraviolet-C (UV-C) light (254nm) in conjunction with nanotechnology in a protective biosafety environment. Shadow regions are best dealt in this system by the generation of hydroxyl radicals (•OH) and negative air ions at sites where UV light cannot penetrate. More than 35 000 negative air ions/cm3 along with •OH were produced continuously in the disinfection chamber through the advanced photocatalytic oxidation process [UV-C + titanium dioxide (TiO2)]. The arrangement has been made to provide an optimized UV irradiation (∼2 mW/cm2) throughout the disinfection system. In order to distinguish between effects arising from (i) the action of UV dose alone and (ii) the action of UV dose along with •OH and negative air ions, E. coli and P. aeruginosa were chosen for bacterial testing and two interventions were made. The first intervention involved placing only UV lamps in the disinfection chamber to see the effect of only UV dose on bacterial inactivation efficiency. The second intervention involved placing the TiO2 nanoparticle coated aluminum plates along with UV lamps; this allows for the generation of negative air ions and •OH inside the disinfection chamber and enhanced bacterial inactivation efficiency. More than 95% bacterial inactivation efficiency has been reported in the case of UV-C + TiO2 compared to only 77% in UV only at the same time interval (90s).

A generalization of the linear adsorption model to include electrosorption

The adsorption phenomenon on surfaces is investigated both with and without the presence of an external electric field. A simple interpretation of the adsorption coefficient and desorption time, as they appear in Langmuir’s isotherm model, is presented. A model for electrosorption is proposed, which explicitly takes into account the applied external voltage and the reaction field resulting from the adsorbed charges. Both saturation, stemming from the finite density of adsorption sites, and non-saturation regimes are considered. The case of a system in contact with a reservoir of particles is also analyzed for its experimental importance. The model’s validity is assessed by analyzing experimental data published by several research groups. A comparative study of the proposed model is conducted in relation to the commonly used pseudo-first and pseudo-second order models. Unlike the latter models, the proposed model allows for the assessment of the impact of the external voltage on the model parameters. The model takes into account ion generation resulting from electrolysis phenomena.

Cu2+ -Anchored Carbon Nano-Photocatalysts for Visible Water Splitting to Boost Hydrogen Cuproptosis.

Both hydrogen (H2 ) and copper ions (Cu+ ) can be used as anti-cancer treatments. However, the continuous generation of H2 molecules and Cu+ in specific sites of tumors is challenging. Here we anchored Cu2+ on carbon photocatalyst (Cu@CDCN) to allow the continuous generation of H2 and hydrogen peroxide (H2 O2 ) in tumors using the two-electron process of visible water splitting. The photocatalytic process also generated redox-active Cu-carbon centers. Meanwhile, the Cu2+ residues reacted with H2 O2 (the obstacle to the photocatalytic process) to accelerate the two-electron process of water splitting and cuprous ion (Cu+ ) generation, in which the Cu2+ residue promoted a pro-oxidant effect with glutathione through metal-reducing actions. Both H2 and Cu+ induced mitochondrial dysfunction and intracellular redox homeostasis destruction, which enabled hydrogen therapy and cuproptosis to inhibit cancer cell growth and suppress tumor growth. Our research is the first attempt to integrate hydrogen therapy and cuproptosis using metal-enhanced visible solar water splitting in nanomedicine, which may provide a safe and effective cancer treatment.

Cu2+‐Anchored Carbon Nano‐Photocatalysts for Visible Water Splitting to Boost Hydrogen Cuproptosis

AbstractBoth hydrogen (H2) and copper ions (Cu+) can be used as anti‐cancer treatments. However, the continuous generation of H2 molecules and Cu+ in specific sites of tumors is challenging. Here we anchored Cu2+ on carbon photocatalyst (Cu@CDCN) to allow the continuous generation of H2 and hydrogen peroxide (H2O2) in tumors using the two‐electron process of visible water splitting. The photocatalytic process also generated redox‐active Cu‐carbon centers. Meanwhile, the Cu2+ residues reacted with H2O2 (the obstacle to the photocatalytic process) to accelerate the two‐electron process of water splitting and cuprous ion (Cu+) generation, in which the Cu2+ residue promoted a pro‐oxidant effect with glutathione through metal‐reducing actions. Both H2 and Cu+ induced mitochondrial dysfunction and intracellular redox homeostasis destruction, which enabled hydrogen therapy and cuproptosis to inhibit cancer cell growth and suppress tumor growth. Our research is the first attempt to integrate hydrogen therapy and cuproptosis using metal‐enhanced visible solar water splitting in nanomedicine, which may provide a safe and effective cancer treatment.

Ultralong Cycle Life and High Rate of Zn‖I2 Battery Enabled by MBene‐Hosted I2 Cathode

AbstractHigh rate tolerance and long cycle life represent the critical demand of the market for energy storage devices, known as one of major challenges for the development of rechargeable aqueous batteries. Herein, a layered Mo4/3B2T2 (where “T” denotes ‐O, ‐OH, and ‐F terminations) MBene (a transition metal boride) with in‐plane ordered metal vacancies is first proposed as an iodine species host of an aqueous Zn‖I2 battery, delivering a discharge capacity of 106.8 mAh g−1 at 25 A g−1 after 230 000 cycles and 80 mAh g−1 at 100 A g−1, far exceeding those of all Zn‖I2 batteries ever reported. The high performance is attributed to the strong affinity with iodine species and accelerated the redox kinetics by the conductive MBene with metal vacancies, as evidenced by the one‐step conversion of I‒/I0 without the generation of I3‒ ions. This work unlocks a new route for the construction of other halide or sulfur electrode batteries with superior durability and kinetics.

Analysis of Pesticide Residues on Fruit Using Swab Spray Ionization Mass Spectrometry.

The vast quantity and high variety of pesticides globally used in agriculture entails considerable risks for the environment and requires ensuring the safety of food products. Therefore, powerful analytical tools are needed to acquire qualitative and quantitative data for monitoring pesticide residues. The development of ambient ionization mass spectrometry methods in the past two decades has demonstrated numerous ways to generate ions under atmospheric conditions and simultaneously to reduce the need for extended sample preparation and circumvent chromatographic separation prior to mass analysis. Swab spray ionization enables the generation of ions directly from swabs via the application of high voltage and solvent flow. In this study, swab sampling of fruit surfaces and subsequent ionization directly from the swab in a modified electrospray ion source was employed for the screening and quantitation of pesticide residues. Aspects regarding sample collection, sampling efficacy on different surfaces, and swab background are discussed. The effect of solvent composition on pesticide-sodium adduct formation and the suppression of ionization by the background matrix have been investigated. Furthermore, a novel approach for the quantitation of pesticide residues based on depletion curve areas is presented. It is demonstrated that swab spray ionization is an effective and quick method for spectral library-based identification and the quantitative analysis of polar contact pesticide residues on food.

Desorption Electrospray Ionization Mass Spectrometry: 20 Years.

ConspectusMass spectrometry (MS) is one of the most widely used technologies in the chemical sciences. With applications spanning the monitoring of reaction products, the identification of disease biomarkers, and the measurement of thermodynamic parameters and aspects of structural biology, MS is well established as a universal analytical tool applicable to small compounds as well as large molecular complexes. Regardless of the application, the generation of gas-phase ions from neutral compounds is a key step in any MS experiment. However, this ionization step was for many years limited to high-energy approaches that required gas-phase analytes and thus it was restricted to volatile samples. Over the last few decades, new methodologies have been developed to address this limitation and facilitate ionization of biological molecules. Electrospray ionization (ESI) is the most broadly used of these methods, as it facilitates the ionization of intact polar compounds from solution.Twenty years ago, our group reported a new ionization method that uses a charged solvent spray to impact a surface, generating ions from objects rather than just solutions and doing so directly in the ambient environment with no vacuum requirements and little to no sample preparation. This method was termed desorption electrospray ionization (DESI), and it initiated a new field that would come to be known as ambient mass spectrometry. The simplicity and wide applicability of the DESI technology─and the tens of ambient ionization methods developed subsequently─revolutionized the MS analysis of complex materials for their organic components, especially for in situ applications.This Account describes the history of DESI, starting with the development of the technique from early electrosonic spray ionization (ESSI) experimental observations as well as the studies leading to the understanding of its mechanism as a "droplet pick-up" phenomenon involving sequential events (i.e., thin film formation, solid-liquid extraction, secondary droplet generation, and ESI-like ionization from these droplets). We also overview the developments and applications of the technology that have been demonstrated by our group during the last two decades. In particular, we describe (i) the use of DESI for tissue imaging, one of its more significant applications to date, and its extension to intraoperative clinical diagnosis; (ii) the integration of the technology with portable instrumentation for in situ analysis, especially when coupled with tandem mass spectrometry (MS/MS); (iii) the use of DESI microdroplets as microvessels to accelerate organic reactions by orders of magnitude compared to those in bulk solution; and (iv) the combination of all these capabilities for automated high-throughput experiments aimed at accelerating drug discovery.

Promoted iron corrosion and enhanced phosphate removal by micro-electric field driven zero-valent iron

Zero-valent iron (Fe0) is restricted in phosphate removal due to the formation of a passive P–Fe layer on its surface. A micro-electric field (0.20 mA cm−2) was employed in Fe0 column to facilitate iron corrosion for enhanced phosphate removal with a Fe0 column as the control. The performance of two columns was compared by batch experiment at a Fe0 filling rate of 10 vol% with quartz sand as dispersing media. The stability and reusability of micro-electric field driven Fe0 (MFD-Fe0) column was estimated by cyclic test. Solid phase analysis showed promoted iron corrosion, iron ion generation, and secondary mineral production such as lepidocrocite and magnetite in the MFD-Fe0 column. Since iron ions tended to precipitate with phosphate, and iron minerals provided reaction sites for phosphate adsorption, the MFD-Fe0 column achieved an enhanced phosphate removal of 94.1%, 2.8 times higher than that of the Fe0 column. The increase of current density from 0 to 0.20 mA cm−2 significantly improved phosphate removal from 24.5% to 94.1%, further demonstrating the promoting effect of micro-electric field on iron corrosion. The MFD-Fe0 column also possessed excellent stability and reusability. It only showed a slight decrease of phosphate removal from 94.1% to 89.7% in eight cycles. It restored a phosphate removal capacity of 97.4% as compared to the initial MFD-Fe0 column by eluting iron (hydro)oxides on Fe0 and quartz sand surfaces with sulfuric acid. This study indicated that MFD-Fe0 is a promising method to remove phosphate from water and an alternative strategy for overcoming Fe0 passivation.

Application of atmospheric pressure field desorption for the analysis of anionic surfactants in commercial detergents

Recent work has shown that field desorption (FD) and field ionization (FI) using activated field emitters may be performed at atmospheric pressure, too. While some limitations apply to atmospheric pressure field desorption (APFD) mass spectrometry (MS), the method can deliver both positive and negative even electron ions of highly polar or ionic compounds. Furthermore, APFD even permits the generation of positive molecular ions of polycyclic aromatic compounds. Here, an application of negative-ion APFD for the analysis of anionic surfactants contained in commercial detergent products for body care, household, and technical uses is presented. The samples include liquid soaps and shower gels, dishwashing liquids, and cooling lubricants. Surfactant solutions in methanol/water or pure methanol at 2–10 µl ml−1 were deposited on commercial 13-µm activated tungsten emitters. The emitters were positioned in front of the atmospheric pressure interface of a Fourier transform-ion cyclotron resonance (FT-ICR) mass spectrometer by means of a slightly modified nano-electrospray ionization (nanoESI) source. The entrance electrode of the interface was set to positive high voltage with respect to the emitter at ground potential. Under these conditions, negative-ion desorption was achieved. The surfactant anions, organic sulfates and organic sulfonates, were characterized by accurate mass-based formula assignments, and in part, by tandem mass spectrometry. The negative-ion APFD spectra were compared to results by negative-ion electrospray ionization (ESI) either obtained using the FT-ICR mass spectrometer or by using a trapped ion mobility-quadrupole-time-of-flight (TIMS-Q-TOF) instrument when product ions of low m/z needed to be detected in tandem MS.Graphical

Multi-Metal Additive Manufacturing with Submicron Resolution by Electrohydrodynamic Redox 3D Printing

The ability to design metals with control over the 3D chemistry at a submicron level unlocks unique possibilities for tailoring and programming their properties. Small scale additive manufacturing of metals has recently shown promising results towards the direct synthesis of chemically heterogeneous 3D geometries. However, the fast and reliable deposition of a wide range of device-grade materials as well as the ability the change the chemistry on-the-fly still pose challenges to the field.Here, we will show how electrohydrodynamic redox (EHD-RP) 3D printing can serve as a toolbox to manufacture multi-metal structures [1]. This technique is based on the dissolution, transfer and re-deposition of metals in solvents using electrochemistry. The on-demand generation of metal ions enables the local modification of the chemical composition in a voxel-by-voxel fashion. The confined electroplating process on the substrates allows feature sizes down to 120 nm, while providing an as-deposited dense microstructure. We’ll focus first on the challenges involved in depositing a large range of metals with EHD-RP [2]. Second, we’ll show how the deposition of metals using different solvents can be combined to manufacture multi-metal structures with a high chemical resolution.[1] A. Reiser, M. Linden, P. Rohner, A. Marchand, H. Galinski, A. S. Sologubenko, J. M. Wheeler, R. Zenobi, D. Poulikakos, and R. Spolenak. Multi-metal electrohydrodynamic redox 3D printing at the submicron scale. Nat. Commun., 10(1):1-8, 2019.[2] M. Nydegger, A. Pruška, H. Galinski, R. Zenobi, A. Reiser and R. Spolenak. Additive Manufacturing of Zn with Submicron Resolution and its Conversion into Zn/ZnO core-shell structures. Nanoscale, 2022

Heterogeneous catalytic reactions of in-situ generated bromide ions via hydrodehalogenation of tetrabromobisphenol A in advanced oxidation processes over palladium nanoparticles

Herein, we report a novel and efficient approach for degrading tetrabromobisphenol A (TBBPA) via catalytic hydrodehalogenation (HDH) and advanced oxidation processes (AOP). Using heterogeneous catalytic HDH of TBBPA over palladium nanoparticles (Pd NPs) achieves the in-situ generation of bromide ions (Br-), which effectively accelerate and reinforce the degradation of debromination intermediates during peroxymonosulfate-based AOP. The conversion of TBBPA to bisphenol A (BPA) by the HDH process reaches up to 99.9% debromination efficiency in 1 h under near-neutral condition, along with the removal of 99.4% BPA in 15 min during the AOP. Further studies show that free bromine and 1O2 produced by in-situ generated Br- reacting with peroxymonosulfate are the most effective reactive species for promoting the BPA degradation. Sustainability footprint analysis reveals considerable stability and high sustainable footprint of the integrated process during long-term operation. This work provides a promising strategy to elimination of bromine organic pollutants in water treatment.

Optimization of an Autonomous Mobile Robot Path Planning Based on Improved Genetic Algorithms

Mobile robots are intended to operate in a variety of environments, and they need to be able to navigate and travel around obstacles, such as objects and barriers. In order to guarantee that the robot will not come into contact with any obstacles or other objects during its movement, algorithms for path planning have been demonstrated. The basic goal while constructing a route is to find the fastest and smoothest route between the starting point and the destination. This article describes route planning using the improvised genetic algorithm with the Bezier Curve (GA-BZ). This study carried out two main experiments, each using a 20x20 random grid map model with varying percentages of obstacles (5%, 15%, and 30% in the first experiment, and 25% and 50% in the second). In the initial experiments, the population (PN), generation (GN), and mutation rate (MR) of genetic algorithms (GA) will be altered to the following values: (PN = 100, 125, 150, or 200; GN = 100, 125, 150; and MR = 0.1, 0.3, 0.5, 0.7) respectively. The goal is to evaluate the effectiveness of AMR in terms of travel distance (m), total time (s), and total cost (RM) in comparison to traditional GA and GA-BZ. The second experiment examined robot performance utilising GA, GA-BZ, Simulated Annealing (SA), A-Star (A*), and Dijkstra's Algorithms (DA) for path distance (m), time travel (s), and fare trip (RM). The simulation results are analysed, compared, and explained. In conclusion, the project is summarised.

Enhancing ion extraction with an inverse sheath in negative hydrogen ion sources for NBI heating

Negative hydrogen ion (H−) sources employed in neutral beam injection (NBI) systems are subject to extraction efficiency issues due to the considerable volumetric losses of negative hydrogen ions. Here, we propose to improve the H− extraction by activating an alternative sheath mode, the electronegative inverse sheath, in front of the H− production surface, which features zero sheath acceleration for H− with a negative sheath potential opposite to the classic sheath. With the inverse sheath activated, the produced H− exhibits smaller gyration, a shorter transport path, less destructive collisions, and therefore higher extraction probability than the commonly believed space-charge-limited (SCL) sheath. Formation of the proposed electronegative inverse sheath and the SCL sheath near the H–-emitting surface is investigated by the continuum kinetic simulation. Dedicated theoretical analyses are also performed to characterize the electronegative inverse sheath properties, which qualitatively agree with the simulation results. We further propose that the transition between the two sheath modes can be realized by tuning the cold ion generation near the emissive boundary. The electronegative inverse sheath is always coupled with a plasma consisting of only hydrogen ions with approximately zero electron concentration, which is reminiscent of the ion–ion plasma reported in previous NBI experiments.