磁尾中交换不稳定性所产生偶极化锋面的动力学特性研究

本文利用考虑了Hall效应和有限Larmor半径(FLR)效应的磁流体数值模拟研究了在离子惯性长度/离子Larmor半径尺度内偶极化锋面的动力学特性.偶极化锋面由磁尾近地区域中由于热压尾向梯度和磁场曲率力不平衡所引起的交换不稳定性自洽产生.数值研究表明,偶极化锋面是切向间断,在相对该锋面结构静止的参考系中等离子体穿过偶极化锋面的法向速度为零.Hall效应主要影响与偶极化锋面的切平面相正交的电场,使得锋面切向电流增大,同时产生锋面结构不对称.研究表明离子在Larmor半径尺度产生的FLR效应可导致锋面结构的大尺度漂移运动.由FLR效应产生的离子磁化流速在偶极化锋面的日下点处指向昏向,锋面后区域的速度晨向分量增长,从而导致整个锋面结构向晨向漂移.

反磁剪切等离子体中的电阻交换模不稳定性

具有内部输运垒（ITB）的反磁剪切（RS）等离子体位形是在托卡马克中获得高参数的最具前景的途径之一。这种位形不仅改善等离子体约束，而且可以改进象气球模和新经典撕裂模等这类宏观模的稳定性。然而，反磁剪切区域的高压强可以驱动电阻交换模不稳定性，从而破坏中心区的等离子体高参数。为了研究电阻交换模不稳定性的性质，并确定其在RS等离子体中发展的区域，我们利用在HL－2A中使用中性束注入建立的RS位形来分析电阻交换模不稳定性。

可压缩Navier-Stokes-Poisson方程的线性稳定性

本文利用稳定性交換准则理论(PES)研究含磁场耦合的可压缩Navier-Stokes-Poisson方程的线性稳定性.研究表明:当无量纲马赫数项1/λ<2π时,方程稳态解(1,0,H 0)是稳定的;当1/λ>2π时,方程的平凡稳态解是不稳定的.

新型球形复合无机离子交换剂的制备及其对锶和铯的去除

用溶胶凝胶的方法制备了新型球形复合无机离子交换剂水合二氧化钛-水合五氧化二锑（HTO-HAP），并以此为基体，进一步制备了磷酸钛-五氧化二锑(TiP-HAP)、 磷酸钛-五氧化二锑-磷钼酸铵(TiP-HAP-AMP)球形复合无机离子交换剂.研究比较了它们对Sr2+和Cs+的离子交换性能和稳定性.结果表明：HTO-HAP在弱酸性条件下对Sr2+和Cs+有较大的交换容量，但耐酸性不好；而作为基体与磷酸反应，或进一步复合磷钼酸铵后，其耐酸性和对Cs+的交换性能均有较大增强.

土星磁层等离子体径向输运的数值模拟

本文建立了一个包含离心力效应的自洽稳态土星磁层模型,并且用等离子体细丝模型对土星磁层等离子体径向输运进行了数值模拟.模拟结果表明,Dione(土卫四)附近的等离子体可能因为发生离心交换不稳定性(Centrifugal Interchange Instability)而被输运到离土星更远的地方.这种输运现象的发生是由离心力主导的,等离子体的黏滞效应和能量转移对输运过程的影响非常小(几乎可以忽略不计),但土星电离层电导率对输运过程有重要影响,电导率越低,径向输运过程越快,反之,高电导率在一定程度上会阻碍输运的进行.在土星电离层电导率σ=2S时,Dione(距离土星6.3RS,RS为土星半径)附近的等离子体在5.52个小时中被输运到距离土星10RS的地方.本文的模拟结果还表明,密度受到扰动的等离子体是不稳定的,如果洛仑兹力和等离子体热压强梯度不能与离心力平衡,径向输运就会发生.密度大的等离子体在向外输运过程中会绝热膨胀而温度降低,密度小的等离子体则在注入磁层过程中因为绝热压缩而温度升高.

Proton-exchange Sulfonated Poly（ether ether ketone）/Sulfonated Phenolphthalein Poly（ether sulfone） Blend Membranes in DMFCs

A sulfonated poly（ether ether ketone） （SPEEK） membrane with fairly high degree of sulfonation （DS） swells excessively and even dissolves at high temperature. To solve these problems, sulfonated phenolphthalein poly（ether sulfone） （SPES-C, DS= 53.7%） is blended with the SPEEK matrix （DS= 55.1%, 61.7%） to prepare SPEEKJSPES-C blend membrane. The decrease in swelling degree and methanol permeability of the membrane is dose-dependent. Pure SPEEK （DS = 61.7%） membrane dissolves completely in water at 70℃, whereas the swelling degree of the SPEEK （DS = 61.7%）/SPES-C （40%, by mass） membrane is 29.7% at 80℃. From room temperature to 80℃, the methanol permeability of all SPEEK （DS = 55.1%）/SPES-C blend membranes is about one order of magnitude lower than that of Nafion 115. At higher temperature, the addition of SPES-C polymer increases the dimensional stability and greater proton conductivity can be achieved. The SPEEK （DS = 55.1%）/SPES-C （40%, by mass） membrane can withstand temperatures up to 150℃. The proton conductivity of SPEEK （DS = 55.1%）/SPES-C （30%, by mass） membrane approaches 0.16 S·cm^-1, matching that of Nafion 115 at 140℃ and 100% RH, while pure SPEEK （DS = 55.1%） membrane dissolves at 90℃. The SPEEK/SPES-C blend membranes are promising for use in direct methanol fuel cells because of their good dimensional stability, high proton conductivity, and low methanol permeability.

Structure and Properties of Hydrotalcite Using Electrostatic Potential Energy Model

The electrostatic potential energy model of hydrotalcites was based on the theory of crystallography. The anionic potential energy of MgAl-hydrotalcites, with 20 layers and 2107 anions per layer, was calculated, and the anionic stability of the hydrotalcites was investigated. The charge density of the layer and the distance between the adjacent anions varied with the molar ratio of Al^3＋/（Mg^2＋ ＋ Al^3＋）. Anionic potential energy depended on the charge and size of the anions. Calculation results remained consistent with thermal stability and the ion exchange ability reported. This model is able to predict anionic stability of the hydrotalcites.

Interatomic diffusion in Pd-Pt core-shell nanoparticles

Pt monolayer-based core-shell catalysts have garnered significant interest for the application of low temperature fuel cell technology as their use may enable a decreased loading of Pt while still providing sufficient current density to meet volumetric requirements. One promising candidate in this class of materials is a Pd@Pt core-shell catalyst, which shows enhanced activity toward oxygen reduction reaction(ORR). One concern with the use of Pd@Pt, however, is the durability of the core-shell structure as Pd atoms are thermodynamically favored to migrate to the surface. The pathway of the migration has not been systematically studied. The current study explores the stability of this structure to thermal annealing and probes the effect of this heat treatment on the catalyst surface structure and its oxygen reduction activity. It was found that surface alloying between Pd and Pt occurs at temperatures as low as 200 °C, and significantly alters the structure and ORR catalytic activity in the range of 200–300 °C. Our results shed lights on the thermal induced interatomic diffusion in all core-shell and thin film structures.

Research on Testing Technologies of Network System in Smart Substations

The network structures of smart substations and the characteristics of industrial Ethernet switches are analyzed.The testing technologies of network systems based on smart substations are specifically elaborated.A viewpoint is proposed that special testing policy&method of smart substation networks should be followed,so that the results can reveal the real network data exchange performance of the whole station.This view ensures the safety and stability of smart substations and lays a foundation for future upgrades and expansions.

Standard-sample bracketing calibration method combined with Mg as an internal standard for silicon isotopic compositions using multi-collector inductively coupled plasma mass spectrometry

Silicon isotope analysis traditionally uses a standard-sample bracketing （SSB） method that relies upon greater instrument stability than can be consistently expected. The following proposed method reduces the level of instrumental stability required for the analysis process and provides a valid solution for high-precision and accurate studies of Si isotopic compositions. Rock samples were dissolved by using alkali fusion and acidification. Silicon isotopes were purified with an ion exchange resin. Interfering peaks for isotopes were separated by using a Nu Plasma 1700 multi-collector inductively coupled plasma mass spectrometry （MS） system in high-resolution mode （M/AM 〉 8000 RP）. Two magnesium isotopes （25Mg and 26Mg） and three silicon isotopes （28Si, 29Si, and 3;Si） were analyzed in the same data collection cycle. Mg isotopes were used as an internal standard to calibrate the mass discrimination effects in MS analysis of Si isotopes in combination with the SSB method in order to reduce the effects of MS interference and instrumental mass dis- crimination on the accuracy of measurements. The conventional SSB method without the Mg internal standard and the proposed SSB method with Mg calibration delivered consistent results within two standard deviations. When Mg was used as an internal standard for calibration, the analysis precision was better than 0.05 %0 amu.

Study on the Stability of Ion-exchange Resin Catalysts:Ⅰ. TGA as a Rapid Evaluating Method

The thermal stability of five commercial ion-exchange resin catalysts was studied by means of thermal gravimetric analysis （TGA） at elevated temperatures of up to 600℃ and isothermal temperatures in the range of 150℃ and 200 ℃. Resin samples with different initial water contents were also investigated. The study indicated that TGA, as a complementary evaluating method for the plug flow reactor system approach, could be used as a fast analyzing means for study on the thermal stability of ion-exchange resin catalysts. The stoichiometric calculation of the isothermally treated resin catalysts based on the FTIR analysis and acid capacity confirmed that the weight loss of the resins at 150℃ and 200℃ was caused by the desulfonation process and that desulfonation occurred mainly at the para-position of the benzene ring in the resins. H＋ ions and moisture played an important role in the desulfonation process.

Chemical regulation of metal halide perovskite nanomaterials for efficient light-emitting diodes

Metal halide perovskite nanomaterials emerged as attractive emitting materials for light-emitting diodes(LEDs) devices due to their high photoluminescence quantum yield(PLQY), narrow bandwidth, high charge-carrier mobility, bandgap tunability, and facile synthesis. In the past few years, it has been witnessed an unprecedented advance in the field of metal halide perovskite nanomaterials based LEDs(Pe LEDs) with a rapid external quantum efficiency(EQE) increase from 0.1% to 14.36%. From the viewpoint of material chemistry, the chemical regulation of metal halide perovskite nanomaterials made a great contribution to the efficiency improvement of Pe LEDs. In this review, we categorize the strategies of chemical regulation as A-site cation engineering, B-site ion doping, X-site ion exchange, dimensional confinement, ligand exchange, surface passivation and interface optimization of transport layers for improving the EQEs of Pe LEDs. We also show the potentials of chemical regulation strategies to enhance the stability of Pe LEDs. Finally, we present insight toward future research directions and an outlook to further improve EQEs and stabilities of Pe LEDs aiming to practical applications.

Anion exchange membranes with eight flexible side-chain cations for improved conductivity and alkaline stability

Increasing the local charge density of flexible side-chain cations in the hydrophilic segments of anion exchange membranes(AEMs)is helpful for improving their properties.However,due to limitations of structural design strategies and available synthetic methods,very few AEMs with more than four flexible side-chain cationic groups in hydrophilic segments have been reported.In order to further improve the hydroxide conductivity,alkaline stability and dimensional stability,herein we report a series of AEMs containing eight flexible side-chain cations in hydrophilic segments,based on poly(aryl ether sulfone)s(PAES).The synthesis,ion exchange capacity(IEC),water absorption,dimensional swelling,alkaline stability and hydroxide conductivity of the obtained membranes(PAES-8TMA-x)were examined and the relationships between structures and properties of different types of AEMs were also systematically compared.The resulting AEMs with IEC values of1.76–2.76 mmol g^-1 displayed comprehensively desirable properties,with hydroxide conductivities of 62.7–92.8 m S cm^-1 and dimensional swelling in the range of 8.3%to15.8%at 60℃.The IEC and hydroxide conductivity for a representative sample,PAES-8TMA-0.35,maintained 82.2%and 79.6%of the initial values after being immersed in2 mol L^-1 Na OH at 90℃ for 480 h,respectively.This study expands the design and preparation of AEMs containing high local densities of flexible side chain cations,and provides a new strategy for new AEM materials.

Dicarboxylate CaC8H4O4 as a high-performance anode for Li-ion batteries

Currently, many organic materials are being considered as electrode materials and display good electrochemical behavior. However, the most critical issues related to the wide use of organic electrodes are their low thermal stability and poor cycling performance due to their high solubility in electrolytes. Focusing on one of the most conventional carboxylate organic materials, namely lithium terephthalate Li2CsH4O4, we tackle these typical disadvantages via modifying its molecular structure by cation substitution. CaCsH4O4 and A12（C8H4O4）3 are prepared via a facile cation exchange reaction. Of these, CaCsH4O4 presents the best cycling performance with thermal stability up to 570℃ and capacity of 399 mA.h.g-1, without any capacity decay in the voltage window of 0.005-3.0 V. The molecular, crystal structure, and morphology of CaCsH4O4 are retained during cycling. This cation-substitution strategy brings new perspectives in the synthesis of new materials as well as broadening the applications of organic materials in Li/Na-ion batteries.

Stable ZnO/ionic liquid hybrid materials: novel dual-responsive superhydrophobic layers to light and anions

Novel dual-responsive superhydrophobic hybrid materials, ZnO/SAMs （self-assembled monolayers） of ionic liquids （ILs） with different counter-anions （I^-, BF4^-, PF6^- and Tf2N^-）, were synthesized and characterized. ZnO nanoparticles were first deposited on glass surfaces to produce roughness. Next, SAMs of fluorinated-alkyl-3-（3-triethoxysilylpropyl）-4,5-dihydro-imidazoliumiodide （abb. [C8Ftespim]I） were grafted onto these surfaces via -Si-O- covalent bonds using self-assembly technique. The I- ion could be subsequently exchanged with BF4, PF6-or Tf2N- through a simple aqueous anion-exchange reaction. The ZnO/ILs hybrid layers were characterized by atomic-force microscopy （AFM）, scanning-electron microscopy （SEM） and X-ray photoelectron spectroscopy （XPS）. Their wettability was estimated through the measurements of static and dynamic contact angles （CAs）. Compared to corresponding films of ZnO/[CsFtespim]I with CAs 140.7° ±2.0°, films of ZnO/[CsFtespim]PF6 and ZnO/[CsFtespim]Tf2N showed CAs with 154.0° ± 2.0° and 152.0° ± 2.0°, respectively that remained for a long time. This result suggests that anion-exchange can afford superhydrophobic materials. In addition, the wettability of ZnO/[CsFtespim]X hybrid layers can be reversibly switched by altering ultraviolet （UV） irradiation and dark storage, which shows a photo-induced reversible switch of wettability. The synergistic action of ZnO nanoparticles and SAMs of ILs produced light-anion dual-responsive superhydrophobic materials with ideal stability.