Integrated analysis of plasma rotation effect on HL-3 hybrid scenario

The hybrid scenario,which has good confinement and moderate MHD instabilities,is a proposed operation scenario for international thermonuclear experimental reactor(ITER).In this work,the effect of plasma rotation on the HL-3 hybrid scenario is analyzed with the integrated modeling framework OMFIT.The results show that toroidal rotation has no obvious effect on confinement with a high line averaged density of n_(bar)~(7)×10^(19)m^(-3).In this case,the ion temperature only changes from 4.7 keV to 4.4 keV with the rotation decreasing from 10^(5) rad/s to 10^(3) rad/s,which means that the turbulent heat transport is not dominant.While in the scenarios characterized by lower densities,such as n_(bar)~4×10^(19)m^(-3),turbulent transport becomes dominant in determining heat transport.The ion temperature rises from 3.8 keV to 6.1 keV in the core as the rotation velocity increases from 10^(3) rad/s to 10^(5) rad/s.Despite the ion temperature rising,the rotation velocity does not obviously affect electron temperature or density.Additionally,it is noteworthy that the variation in rotation velocity does not significantly affect the global confinement of plasma in scenarios with low density or with high density.

Asymmetric orbital hybridization in Zn-doped antiperovskite Cu_(1-x)Zn_(x)NMn_(3)enables highly efficient electrocatalytic hydrogen production

Rational design of efficient and robust earth-abundant alkaline hydrogen evolution reaction(HER)catalysts is a key factor for developing energy conversion technologies.Currently,antiperovskite nitride CuNMn_(3)has garnered significant interest due to its remarkable properties such as negative/zero thermal expansion and magnetocaloric effects.However,when utilized as hydrogen evolution catalysts,it encounters large challenge resulting from excessively strong/weak interactions with adsorbed H on Mn/Cu active sites,which leads to low HER activity.In this study,we introduce an asymmetric orbital hybridization strategy in Zn-doped Cu_(1-x)Zn_(x)NMn_(3)by leveraging the localization of Zn electronic states to reconfigure the electronic structures of Cu and Mn,thereby reducing the energy barrier for water dissociation and optimizing Cu and Mn active sites for hydrogen adsorption and H_(2)production.Electrochemical evaluations reveal that Cu_(0.85)Zn_(0.15)NMn_(3)with x=0.15 demonstrates exceptional electrocatalytic activity in alkaline electrolytes.A low overpotential of 52 mV at 10 mA cm^(-2)and outstanding stability over a 150-h test period are achieved,surpassing commercial Pt/C.This research offers a novel strategy for enhancing HER performance by modulating asymmetric hybridization of electron orbitals between multiple metal atoms within a material structure.

Co_(3)S_(4)-pyrolysis lotus fiber flexible textile as a hybrid electrocatalyst for overall water splitting

Electrocatalytic overall water splitting(OWS),a pivotal approach in addressing the global energy crisis,aims to produce hydrogen and oxygen.However,most of the catalysts in powder form are adhesively bounding to the electrodes,resulting in catalyst detachment by bubble generation and other uncertain interference,and eventually reducing the OWS performance.To surmount this challenge,we synthesized a hybrid material of Co_(3)S_(4)-pyrolysis lotus fiber(labeled as Co_(3)S_(4)-p LF)textile by hydrothermal and hightemperature pyrolysis processes for electrocatalytic OWS.Owing to the natural LF textile exposing the uniformly distributed functional groups(AOH,ANH_(2),etc.)to anchor Co_(3)S_(4)nanoparticles with hierarchical porous structure and outstanding hydrophily,the hybrid Co_(3)S_(4)-p LF catalyst shows low overpotentials at 10 m A cm^(-2)(η_(10,HER)=100 m Vη_(10,OER)=240 mV)alongside prolonged operational stability during electrocatalytic reactions.Theoretical calculations reveal that the electron transfer from p LF to Co_(3)S_(4)in the hybrid Co_(3)S_(4)-p LF is beneficial to the electrocatalytic process.This work will shed light on the development of nature-inspired carbon-based materials in hybrid electrocatalysts for OWS.

Understanding the roles of Brønsted/Lewis acid sites on manganese oxide-zeolite hybrid catalysts for low-temperature NH_(3)-SCR

Although metal oxide-zeolite hybrid materials have long been known to achieve enhanced catalytic activity and selectivity in NO_(x)removal reactions through the inter-particle diffusion of intermediate species,their subsequent reaction mechanism on acid sites is still unclear and requires investigation.In this study,the distribution of Brønsted/Lewis acid sites in the hybrid materials was precisely adjusted by introducing potassium ions,which not only selectively bind to Brønsted acid sites but also potentially affect the formation and diffusion of activated NO species.Systematic in situ diffuse reflectance infrared Fourier transform spectroscopy analyses coupled with selective catalytic reduction of NO_(x)with NH_(3)(NH_(3)-SCR)reaction demonstrate that the Lewis acid sites over MnO_(x)are more active for NO reduction but have lower selectivity to N_(2)than Brønsted acids sites.Brønsted acid sites primarily produce N_(2),whereas Lewis acid sites primarily produce N_(2)O,contributing to unfavorable N_(2)selectivity.The Brønsted acid sites present in Y zeolite,which are stronger than those on MnO_(x),accelerate the NH_(3)-SCR reaction in which the nitrite/nitrate species diffused from the MnO_(x)particles rapidly convert into the N_(2).Therefore,it is important to design the catalyst so that the activated NO species formed in MnO_(x)diffuse to and are selectively decomposed on the Brønsted acid sites of H-Y zeolite rather than that of MnO_(x)particle.For the physically mixed H-MnO_(x)+H-Y sample,the abundant Brønsted/Lewis acid sites in H-MnO_(x)give rise to significant consumption of activated NO species before their inter-particle diffusion,thereby hindering the enhancement of the synergistic effects.Furthermore,we found that the intercalated K+in K-MnO_(x)has an unexpected favorable role in the NO reduction rate,probably owing to faster diffusion of the activated NO species on K-MnO_(x)than H-MnO_(x).This study will help to design promising metal oxide-zeolite hybrid catalysts by identifying the role of the acid sites in two different constituents.

Hierarchical FeO_(χ)H_(y)@Ni_(3)B hybrid for efficient alkaline oxygen evolution at high current density

Electrocatalysts with high activity and long-term durability are vital toward large-scale hydrogen pro-duction from electrocatalytic water splitting.Here,the self-supported electrode(FeO_(χ)H_(y)@Ni_(3)B/NF)with hierarchical heterostructure was simply prepared by using Ni_(3)B chunks grown on nickel foam as sub-strate to in situ form vertical FeO_(χ)H_(y)nanosheets.Such hybrid shows efficient oxygen evolution reaction activity with overpotentials as low as 267 and 249 mV at 100 mA cm^(-2)in 1 M KOH solution and 30 wt%KOH solution,respectively.Meanwhile,it also exhibits excellent catalytic stability,sustaining catalysis at 500 mA cm^(-2)in 1 M KOH solution for 200 h,and even for 200 h at 1000 mA cm^(-2)in 30 wt%KOH solution.Further experimental results reveal that the FeO_(χ)H_(y)@Ni_(3)B/NF is endowed with superhydrophilic and superaerophobic surface properties,which not only provide more mass transport channels,as well as facilitated the diffusion of reaction intermediates and gas bubbles.Also,it holds faster reaction kinetics,more accessible active sites and accelerated electron transfer rates due to strong synergistic interactions attheheterogeneous interface.

Electrochemical Activation-Induced Structural Transformation in Ni(OH)_(2)/Ti_(3)C_(2)T_(x)/NF Systems with Enhanced Electrochemical Performance for Hybrid Supercapacitors

Exploring a novel strategy for large-scale production of battery-type Ni(OH)_(2)-based composites,with excellent capacitive performance,is still greatly challenging.Herein,we developed a facile and cost-effective strategy to in situ grow a layer of Ni(OH)_(2)/Ti_(3)C_(2)T_(x)composite on the nickel foam(NF)collector,where Ti_(3)C_(2)T_(x)is not only a conductive component,but also a catalyst that accelerates the oxidation of NF to Ni(OH)_(2).Detailed analysis reveals that the crystallinity,morphology,and electronic structure of the integrated electrode can be tuned via the electrochemical activation,which is beneficial for improving electrical conductivity and redox activity.As expected,the integrated electrode shows a specific capacity of 1.09 C cm^(-2)at 1 mA cm^(-2)after three custom activation cycles and maintains 92.4%of the initial capacity after 1500 cycles.Moreover,a hybrid supercapacitor composed of Ni(OH)_(2)/Ti_(3)C_(2)T_(x)/NF cathode and activated carbon anode provides an energy density of 0.1 mWh cm^(-2)at a power density of 0.97 mW cm^(-2),and excellent cycling stability with about 110%capacity retention rate after 5000 cycles.This work would afford an economical and convenient method to steer commercial Ni foam into advanced Ni(OH)_(2)-based composite materials as binder-free electrodes for hybrid supercapacitors.

Contribution to the Full 3D Finite Element Modelling of a Hybrid Stepping Motor with and without Current in the Coils

The paper presents our contribution to the full 3D finite element modelling of a hybrid stepping motor using COMSOL Multiphysics software. This type of four-phase motor has a permanent magnet interposed between the two identical and coaxial half stators. The calculation of the field with or without current in the windings (respectively with or without permanent magnet) is done using a mixed formulation with strong coupling. In addition, the local high saturation of the ferromagnetic material and the radial and axial components of the magnetic flux are taken into account. The results obtained make it possible to clearly observe, as a function of the intensity of the bus current or the remanent induction, the saturation zones, the lines, the orientations and the magnetic flux densities. 3D finite element modelling provide more accurate numerical data on the magnetic field through multiphysics analysis. This analysis considers the actual operating conditions and leads to the design of an optimized machine structure, with or without current in the windings and/or permanent magnet.

Hybrid ETKF-3DVAR方法同化多普勒雷达速度观测资料Ⅰ:模拟资料试验

利用WRF(Weather research and forecasting)模式及模式模拟的资料,采用Hybrid ETKF-3DVAR(ensemble transform Kalman filter-three-dimensional variational data assimilation)方法同化模拟雷达观测资料。该混合同化方法将集合转换卡尔曼滤波(ensemble transform Kalman filter)得到的集合样本扰动通过转换矩阵直接作用到背景场上,利用顺序滤波的思想得到分析扰动场;然后通过增加额外控制变量的方式把"流依赖"的集合协方差信息引入到变分目标函数中去,在3DVAR框架基础下与观测数据进行融合,从而给出分析场的最优估计。试验结果表明,Hybrid ETKF-3DVAR同化方法相比传统3DVAR可以提供更为准确的分析场,Hybrid方法雷达资料初始化模拟的台风涡旋结构与位置比3DVAR更加接近"真实场",对台风路径预报也有明显改进。通过对比Hybrid S试验与Hybrid F试验发现,Hybrid的正效果主要来源于混合背景误差协方差中的"流依赖"信息,集合平均场代替确定性背景场带来的效果并不显著。

基于Hybrid EnSRF-En3DVar的雷达资料同化研究

基于WRF模式构建了Hybrid En SRF-En3DVar同化系统,该系统使用En SRF方案直接更新集合扰动。利用构建的同化系统针对台风"桑美"分别进行集合协方差权重敏感性试验和同化雷达不同观测资料的敏感性试验。集合协方差权重敏感性试验发现:当集合协方差权重分别为0.25、0.5和0.75时,同化效果优于3DVar试验,其中0.75的集合协方差权重试验得到了分析场的最优估计;当集合协方差权重为1.0时,分析场最差。同化雷达不同观测资料的敏感性试验表明,联合同化雷达径向风及反射率能有效改善大气湿度场和风场,但对风场的改善效果不如仅同化雷达径向风好。将En SRF集合扰动更新方案与扰动观测方案综合分析发现,扰动观测方案集合离散度较小,计算代价大,En SRF方案优于扰动观测方案。

A New Towel Gourd F_1 hybrid——‘Taisi NO.3'

＇Taisi N0.3＇ is an early mid-maturing towel gourd F1 hybrid developed by crossing Ps17-6-5-2-10-8 as female parent and Ps39-3-8-4-6-5 as male parent. The period from sowing to first harvest is about 75 days in spring cropping. It grows exuberantly in early stage and better in middle and later stages; leaves are green and palmately divided; the maximum leaf＇s length and width are about 25.5 and 33.7 cm. It bears fruit at the main and lateral branch. The first female flower sets on the 7^th-8^th node, and the fruit-setting rate is 72.8%. The fruit-setting rate is high. Its fruit is long round stick shape, 47.4 cm in length, and 3.75 cm in width, with smooth and green skin covered by dark green stripes, dense flesh. The fruit tastes good, with high Vc content. It is resistant to downy mildew, moderately resistant to CMV, and highly resistant to blight. The average fruit weight is about 282.3 g with the general yield of 82 500 kg/hm2.

新(3+1)维KP方程的退化解与相互作用解

该文主要研究了由Wazwaz于2022年首次提出的新(3+1)维KP方程的非线性波解.基于Hirota双线性形式,利用模共振技术由N-孤子解得到P-呼吸解.然后,利用参数极限法,根据参数的特殊关系,对同宿呼吸解和N-孤子解进行退化得到了Lump解.最后,从N-孤子解的部分退化出发,研究了由呼吸解、孤子解和Lump解组成的相互作用解.该文通过可视化图形展示了这些解的动力学特性.

An insight into failure mechanism of NASICON-structured Na3V2（PO4）3 in hybrid aqueous rechargeable battery

NASICON (Na-super-ionic-conductors)-structured materials have attracted extensive research interest due to their great application potential in secondary batteries. However, the mechanism of capacity fading for NASICON-structured electrode materials has been rarely studied. In this paper, we synthesized the NASICON-structured Na3V2(PO4)3/C composite by simple sol-gel and high-temperature solid-phase method and investigated its electrochemical performance in Na-Zn hybrid aqueous rechargeable batteries. After characterizing the structure, morphology and composition variations as well as the interfacial resistance changes of Na3V2(PO4)3/C cathode during cycling, we propose a mechanical and interfacial degradation mechanism for capacity fading of NASICON-structured Na3V2(PO4)3/C in Na-Zn hybrid aqueous rechargeable batteries. This work will shed light on enhancing the mechanical and in terfacial stability of NASICON-structured Na3V2(PO4)3/C in Na-Zn hybrid aqueous rechargeable batteries.

AgCl/Ag/g-C_3N_4 Hybrid Composites: Preparation,Visible Light-Driven Photocatalytic Activity and Mechanism

The ternary plasmonic Ag Cl/Ag/g-C_3N_4 photocatalysts were successfully fabricated by a modified deposition–precipitation method, through which Ag/Ag Cl nanoparticles(5–15 nm in size) were evenly dispersed on the surface of g-C_3N_4. The Ag Cl/Ag/g-C_3N_4 composites exhibited higher photocatalytic activity than Ag/Ag Cl and g-C_3N_4. The enhanced photocatalytic performance could be attributed to an efficient separation of electron–hole pairs through a Z-scheme mechanism, in which Ag nanoparticles acted as charge separation centers.

In-Situ Annealed Ti_(3)C_(2)T_(x) MXene Based All-Solid-State Flexible Zn-Ion Hybrid Micro Supercapacitor Array with Enhanced Stability

Zn-ion hybrid supercapacitors(SCs)are considered as promising energy storage owing to their high energy density compared to traditional SCs.How to realize the miniaturization,patterning,and flexibility of the Zn-ion SCs without affecting the electrochemical performances has special meanings for expanding their applications in wearable integrated electronics.Ti_(3)C_(2)T_(x) cathode with outstanding conductivity,unique lamellar structure and good mechanical flexibility has been demonstrated tremen-dous potential in the design of Zn-ion SCs,but achieving long cycling stability and high rate stability is still big challenges.Here,we proposed a facile laser writing approach to fabricate patterned Ti_(3)C_(2)T_(x)-based Zn-ion micro-supercapacitors(MSCs),followed by the in-situ anneal treatment of the assembled MSCs to improve the long-term stability,which exhibits 80%of the capacitance retention even after 50,000 charge/discharge cycles and superior rate stability.The influence of the cathode thickness on the electrochemical performance of the MSCs is also studied.When the thickness reaches 0.851μm the maximum areal capacitance of 72.02 mF cm^(−2)at scan rate of 10 mV s^(−1),which is 1.77 times higher than that with a thickness of 0.329μm(35.6 mF cm^(−2)).Moreover,the fab-ricated Ti_(3)C_(2)T_(x) based Zn-ion MSCs have excellent flexibility,a digital timer can be driven by the single device even under bending state,a flexible LED displayer of“TiC”logo also can be easily lighted by the MSC arrays under twisting,crimping,and winding conditions,demonstrating the scalable fabrication and application of the fabricated MSCs in portable electronics.

Intrinsic Instability of the Hybrid Halide Perovskite Semiconductor CH3NH3PbI3

The organic-inorganic hybrid perovskite CH3NH3PbI3 has attracted significant interest for its high performance in converting solar light into electrical power with an efficiency exceeding 20%. Unfortunately, chemical stability is one major challenge in the development of CH3NH3PbI3 solar cells. It was commonly assumed that moisture or oxygen in the environment causes the poor stability of hybrid halide perovskites, however, here we show from the first-principles calculations that the room-temperature tetragonal phase of CH3NH3PbI3 is thermodynamically unstable with respect to the phase separation into CH3NH3I ＋ PbI2, i.e., the disproportionation is exothermic, independent of the humidity or oxygen in the atmosphere. When the structure is distorted to the low-temperature orthorhombie phase, the energetic cost of separation increases, but remains small. Contributions from vibrational and configurational entropy at room temperature have been considered, but the instability of CH3NH3PbI3 is unchanged. When I is replaced by Br or CI, Pb by Sn, or the organic cation CH3NH3 by inorganic Cs, the perovskites become more stable and do not phase-separate spontaneously. Our study highlights that the poor chemical stability is intrinsic to CH3NH3PbI3 and suggests that element-substitution may solve the chemical stability problem in hybrid halide perovskite solar cells.

Optimization of fermentation conditions for P450 BM-3 monooxygenase production by hybrid design methodology

Factorial design and response surface techniques were used to design and optimize increasing P450 BM-3 expression in E, coll. Operational conditions for maximum production were determined with twelve parameters under consideration： the concentration of FeCl3, induction at OD578 （optical density measured at 578 nm）, induction time and inoculum concentration. Initially, Plackett-Burman （PB） design was used to evaluate the process variables relevant in relation to P450 BM-3 production. Four statistically significant parameters for response were selected and utilized in order to optimize the process. With the 416C model of hybrid design, response surfaces were generated, and P450 BM-3 production was improved to 57.90×10^-3 U/ml by the best combinations of the physicochemical parameters at optimum levels of 0,12 mg/L FeCl3, inoculum concentration of 2.10%, induction at OD578 equal to 1.07, and with 6.05 h of induction.

Fast ion diffusion alloy layer facilitating 3D mesh substrate for dendrite-free zinc-ion hybrid capacitors

Although aqueous zinc ion hybrid capacitors have advantageous integration of batteries and supercapacitors,they still suffer from the inherent problems of dendrite growth and interfacial side reactions on Zn anodes.Herein,a universal fast zinc-ion diffusion layer on a three-dimensional(3 D)mesh structure model is demonstrated to effectively improve Zn plating/stripping reversibility.The fast ion diffusion alloy layer accelerates the Zn^(2+)migration in an orderly manner to homogenize Zn^(2+)flux and overcomes the defects of the commercial mesh substrate,effectively avoiding dendrite growth and side reactions.Consequently,the proof-of-concept silver-zinc alloy modified stainless steel mesh delivers superb reversibility with the high coulombic efficiency over 99.4%at 4 mA cm^(-2)after 1600 cycles and excellent reliability of over 830 h at 1 mA cm^(-2),Its feasibility is also evidenced in commercial zinc ion hybrid capacitors with activated carbon as the cathode.This work enriches the fundamental comprehension of fast zinc-ion diffusion layer combined with a 3 D substrate on the Zn deposition and opens a universal approach to design advanced host for Zn electrodes in zinc ion hybrid capacitors.

Comparison of dry reforming of methane in low temperature hybrid plasma-catalytic corona with thermal catalytic reactor over Ni/γ-Al_2O_3

In the current study, the hybrid effect of a corona discharge and γ-alumina supported Ni catalysts in CO2 reforming of methane is investigated. The study includes both purely catalytic operation in the temperature range of 923-1023 K, and hybrid catalytic-plasma operation of DC corona discharge reactor at room temperature and ambient pressure. The effect of feed flow rate, discharge power and Ni/γ-Al2O3 catalysts are studied. When CH4/CO2 ratio in the feed is 1/2, the syngas of low Ha/CO ratio at about 0.56 is obtained, which is a potential feedstock for synthesis of liquid hydrocarbons. Although Ni catalyst is only active above 573 K, presence of Ni catalysts in the cold corona plasma reactor （T≤523 K） shows promising increase in the conversions of methane and carbon dioxide. When Ni catalysts are used in the plasma reaction, H2/CO ratios in the products are slightly modified, selectivity to CO increases whereas fewer by-products such as hydrocarbons and oxygenates are formed.

Hybrid battery integrated by Zn-air and Zn-Co3O4 batteries at cell level

The construction of Zn based hybrid battery through the combination of Zn-air and Zn-Co3O4 batteries at cell level is a feasible strategy to integrate high voltage,specific capacity and energy density in one power supply equipment.For Zn based hybrid battery,an efficient cathode material with high specific capacitance and excellent ORR,OER activities is a vital component,which determines its performance in great extent.In this work,with Co based coordination polymer as precursor,oxygen vacancy-rich Co3 O4 based cathode material is synthesized.In this material Co3O4 particles with the size about 20 to 35 nm reside evenly in mesoporous carbon matrix doped by nitrogen atoms.In OER,the overpotential of this cathode material is merely 330 m V.Its ORR proceeds with a typical four electron process with half wave achieving 0.76 V.If charge/discharge at 1 A·g^-1,specific capacitance of this cathode material is 254.4 mAh·g^-1.As current density increases to 20 A·g^-1,the specific capacitance still arrives at 122.5 mAh·g^-1 with nearly 50%retained.Based on attractive performance of this cathode material,Zn based hybrid battery is assembled.When discharge at 1 m A·cm-2,it presences two voltage platforms at 1.71 and 1.14 V.In this situation,specific capacitance reaches 790 m Ah·g^-1 with energy density 928 Wh·kg^-1.Hybrid battery shows promising stability after 300-cycle continuous test.

A General Self-Sacrifice Template Strategy to 3D Heteroatom-Doped Macroporous Carbon for High-Performance Potassium-Ion Hybrid Capacitors

Potassium-ion hybrid capacitors(PIHCs)tactfully combining capacitor-type cathode with battery-type anode have recently attracted increasing attentions due to their advantages of decent energy density,high power density,and low cost;the mismatches of capacity and kinetics between capacitor-type cathode and battery-type anode in PIHCs yet hinder their overall performance output.Herein,based on prediction of density functional theory calculations,we find Se/N co-doped porous carbon is a promising candidate for K+storage and thus develop a simple and universal self-sacrifice template method to fabricate Se and N co-doped three-dimensional(3D)macroporous carbon(Se/N-3DMpC),which features favorable properties of connective hier-archical pores,expanded interlayer structure,and rich activity site for boosting pseudocapacitive activity and kinetics toward K^(+)storage anode and enhancing capacitance performance for the reversible anion adsorption/desorption cath-ode.As expected,the as-assembled PIHCs full cell with a working voltage as high as 4.0 V delivers a high energy density of 186 Wh kg^(−1) and a power output of 8100 W kg^(−1) as well as excellent long service life.The proof-of-concept PIHCs with excellent performance open a new avenue for the development and application of high-performance hybrid capacitors.