常压He气和N$lt;sub$gt;2$lt;/sub$gt;气均匀介质阻挡放电的伏安特性

对带有多电流峰的常压He气均匀介质阻挡放电与常压N₂气均匀介质阻挡放电的伏安特性进行了实验分析. 分析结果表明：实验结果与模拟结果相符. 在带有多电流峰的常压He均匀介质阻挡放电中,辉光放电模式和汤森放电模式可以共存于一个多电流放电序列内. 此外,在放电电流增长阶段,可以根据常压均匀介质阻挡放电的伏安特性曲线的微分电导来判断均匀介质阻挡放电的放电模式. 在放电电流增长阶段,如果电流脉冲的伏安特性曲线呈现负微分电导,则电流脉冲为辉光放电模式;如果呈现正微分电导,则为汤森放电模式. 由此可以判断,常压N₂气均匀介质阻挡放电为汤森放电模式. 关键词： 伏安特性 辉光放电模式 汤森放电模式 常压均匀介质阻挡放电     

介质阻挡放电丝模式和均匀模式转化的特性

利用水电极介质阻挡放电装置,采用电学方法和发射光谱,研究了空气中介质阻挡放电从微放电丝模式向均匀放电模式转化的过程. 结果表明,大气压下增大外加电压或者电压一定减小气压,放电都能够从微放电丝模式过渡到均匀模式. 高气压下放电为流光击穿而低气压下为辉光放电. 利用放电发射光谱,研究了高能电子比例随实验参数的变化. 结果表明气压减小时高能电子比例增大,电压增加时高能电子减少. 利用壁电荷理论对以上实验结果进行了定性分析. 结果对介质阻挡均匀放电的深入研究具有重要价值. 关键词： 介质阻挡放电 光学发射谱 微放电丝 均匀放电模式     

大气压介质阻挡丝状放电时空演化数值模拟

通过数值求解二维流体方程，在均匀的初始条件下研究了大气压丝状放电的整体时空演化.通过模拟可以发现，在丝状放电的时空演化过程中，各条放电通道在不同位置相继发生击穿，且放电通道有遍历整个放电空间的趋势.在一定条件下，放电通道还会发生分裂与合并现象，其中放电通道的分裂导致了放电空间中放电通道的增加，而放电通道的合并则提供了一条放电空间中放电通道减少的途径.研究还表明，介质表面电荷是影响丝状放电整体时空演化的关键因素之一. 关键词： 介质阻挡放电 丝状放电 数值模拟 时空演化     

大气压等离子体针产生空气均匀放电特性研究

大气压空气放电由于脱离了真空装置,易于实现流水线生产,因而在工业上具有广泛的应用. 采用等离子体针装置在空气中产生了稳定的大气压均匀放电. 利用光谱法对等离子体的相关参数进行了空间分辨率测量,并通过光学方法对放电机理进行了研究. 结果表明,等离子体针产生的放电存在电晕放电和等离子体羽放电两种模式. 在稳定的等离子体羽放电模式中,发光分为强光区和弱光区. 弱光区放电的发展速度远大于强光区的发展速度,电子能量和电子密度均是弱光区比强光区大. 对均匀放电的气体温度和振动温度的研究表明,强光区放电遵循汤生击穿机理而弱光区为流光放电. 这些结果对大气压空气放电的工业应用具有重要意义. 关键词： 大气压均匀放电 等离子体针 发射光谱 放电机理     

针-板DBD微流注与微辉光交替生成的机理研究

在介质阻挡放电体系中产生辉光放电可以有效的提高放电体系产生高能电子的性能, 为等离子体化学反应提供更加丰富的活性粒子.本文对针-板介质阻挡放电体系下的放电模式进行了研究,实验发现放电正负半周期表现出不同的放电模式, 激励电压为3 kV时放电正负半周期分别为微流注放电和电晕放电(或者Trichel脉冲放电),激励电压为6 kV时放电正负半周期分别为微流注放电和微辉光放电.微辉光放电形貌具有与典型辉光放电相同的分层次放电结构, 分析了激励电压6 kV时的放电过程,认为足够强的阴极电场强度和裸露针状电极形成的有效的二次电子发射过程是形成微辉光放电的主要因素,绝缘介质层的存在避免了微辉光放电向弧光放电过渡.     

大气压氦气介质阻挡放电单-多柱演化动力学

介质阻挡放电被众多工业领域用作低温等离子体源,柱状放电是介质阻挡放电的重要形式之一,但其放电理论尚未掌握.进行大气压氦气介质阻挡放电实验,通过降低外施电压低于起始放电电压实现了柱状放电从单柱到多柱的斑图演化,拍摄了电极底面放电图像,测量了外施电压、放电电流、放电转移电荷、放电柱的柱直径和柱间距,计算了放电柱受其他所有柱施加的库仑力与磁场力.结果表明:外施电压变化瞬间电极底面放电图像呈现出动态演化过程.不同层放电柱的柱直径由中心向外层依次增大.计算发现演化稳定后放电柱所受库仑力远大于磁场力,推理存在一约束势平衡库仑力使放电柱稳定分布.不同电压、位置的放电柱所受库仑力不同:不同层的放电柱所受库仑力由最外层至中心柱依次减小,中心柱受力为0,最外层放电柱的约束势应最大而中心放电柱的约束势应该最小;外施电压降低,介质表面电荷和放电柱总数的共同作用导致库仑力增大,约束势也应有所增大,即约束势受介质表面电荷、放电柱总数与位置的共同影响.     

介质阻挡放电丝模式和均匀模式转化的特性

利用水电极介质阻挡放电装置，采用电学方法和发射光谱，研究了空气中介质阻挡放电从微放电丝模式向均匀放电模式转化的过程. 结果表明，大气压下增大外加电压或者电压一定减小气压，放电都能够从微放电丝模式过渡到均匀模式. 高气压下放电为流光击穿而低气压下为辉光放电. 利用放电发射光谱，研究了高能电子比例随实验参数的变化. 结果表明气压减小时高能电子比例增大，电压增加时高能电子减少. 利用壁电荷理论对以上实验结果进行了定性分析. 结果对介质阻挡均匀放电的深入研究具有重要价值.     

介质阻挡放电中微放电的映射方程

利用双水电极介质阻挡放电装置，采用光学方法测量了大气压空气和氩气中介质阻挡放电的微放电时间特性.实验发现微放电通道相邻两次放电时间间隔是长短交替的.根据壁电荷对相邻两次微放电的不同影响，建立了介质阻挡放电时间序列的映射方程.不同放电参量取值情况下的计算结果表明，介质阻挡放电中，壁电荷电场的衰减时间常数远大于100μs量级.由方程所得的结果，解释了相邻两次放电时间间隔长短交替的实验现象，确定了壁电荷衰减时间常数的范围. 关键词： 介质阻挡放电 时间特性 壁电荷 映射方程     

液体电极上辉光放电丝的运动特性研究

大气压液体电极放电在生物医疗、化学降解、环境保护等众多方面具有广泛的应用前景,引起了研究者的关注.本文利用直流电压激励棒-水电极装置,在6 mm气隙间产生了大气压辉光放电.研究发现,随着电流的增大,放电由锥状转变成柱状,且此过程中水面上放电环的直径先增大后减小.利用高速照相机对放电进行研究,发现锥状放电是由单个放电丝旋转形成的.通过测量放电的伏安特性,表明放电处于正常辉光机理.利用光谱学方法,研究了不同电流下的振动温度、转动温度和谱线强度比I_(391.4)/I_(337.1),发现它们均随电流的增加而增大.根据气体放电理论,分析和解释了放电丝的运动机理,并对水面上放电环直径随电流的变化关系进行了解释.这些结果对于大气压液体电极放电的理论研究和实际应用均具有一定参考价值.     

气流对微秒脉冲滑动放电特性的影响

脉冲电源驱动的滑动放电能够在大气压下产生高能量、高功率密度的低温等离子体. 为了研究微秒脉冲电源在针-针电极结构中产生滑动放电的特征, 本文采用电压幅值为0–30 kV, 脉冲宽度约8 μs, 脉冲重复频率为1–3000 Hz的微秒脉冲电源, 通过测量电压、电流波形和拍摄放电图像, 研究了微秒脉冲滑动放电的电特性. 实验结果表明, 随着施加电压的增加微秒脉冲滑动放电存在三种典型的放电模式: 电晕放电、弥散放电和类滑动放电. 不同放电模式的电压、电流波形和放电图像之间差异显著. 脉冲重复频率对微秒脉冲滑动放电特性有影响, 表现为当气体流量较小(2 L/min)时, 类滑动放电的放电通道随着脉冲重复频率的增大逐渐集中, 而当气体流量较大(16 L/min)时, 类滑动放电的放电通道随着脉冲重复频率的增大逐渐分散. 不同气流下重复频率对滑动放电特性的影响与放电中粒子的记忆效应和气流的状态有关.     

双预电离对TEA CO_2激光器放电特性的影响

一些低增益弱线CO2激光光谱在分离某种同位素方面是非常有用的。在成比例的混合气体中很难获得这些谱线的输出,须适当提高CO2和N2的含量,但结果给主电极的辉光放电带来了困难。通过对改装后的双预电离放电回路的参量进行调节,实现了对预电离的单独控制,有利于增强预电离效果,使高含量的CO2混合气体的放电和出光成为可能。理论和实验证明了双预电离能较好地改善TEA CO2激光器的放电性能,尤其是有望实现用于分离某些同位素的弱线输出。     

Electrical and optical characterization of pulsed plasma of N<Subscript>2</Subscript>–H<Subscript>2</Subscript>

This paper considers the electrical and optical characterization of glow discharge pulsed plasma in N₂/H₂ gas mixtures at a pressures range between 0.5 and 4.0 Torr and discharge current between 0.2 and 0.6 A. Electron temperature and ion density measurements were performed employing a double Langmuir probe. They were found to increase rapidly as the H₂ percentage in the mixture was increased up to 20%. This increase slows down as the H₂ percentage in the gas mixture was increased above 20% at the same pressure. Emission spectroscopy was employed to observe emission from the pulsed plasma of a steady-state electric discharge. The discharge mainly emits within the range 280–500 nm. The emission consists of N₂ (C-X) 316, 336, 358 nm narrow peaks and a broad band with a maximum at λ_max = 427 nm. Also lines of N₂, N₂ ⁺ and NH excited states were observed. All lines and bands have their maximum intensity at the discharge current of 0.417 A. The intensities of the main bands and spectral lines are determined as functions of the total pressure and discharge current. Agreement with other theoretical and experimental groups was established.     

氧化石墨制备温度对石墨烯结构及其锂离子电池性能的影响

采用改进的Hummers 法, 以石墨粉为原料制备氧化石墨, 然后使用微波还原法制备石墨烯, 最后以石墨烯作为负极材料组装锂离子电池. 系统的研究了高温氧化阶段中温度对氧化石墨的氧化程度、石墨烯的还原程度和比表面积以及锂离子电池性能的影响. 利用场发射扫描电镜(FESEM)、 X射线光电子能谱(XPS)、X射线衍射仪(XRD)、BET测量仪对氧化石墨和石墨烯的微观结构及比表面积等进行测试和表征. XRD, XPS及电化学测试的结果显示当高温阶段氧化温度为90 °C时, 氧化石墨的氧化程度最高, 相应的石墨烯也具有最高的还原程度和最大的比表面积423.2 m²/g, 同时石墨烯锂离子电池也具有更好的性能: 首次放电比容量为1555.5 mAh/g, 充电容量为1024.6 mAh/g, 其循环放电比容量达到600 mAh/g.     

Study on the surface properties of wood/polyethylene composites treated under plasma

Wood/polyethylene (PE) composites are widely used in many fields for its excellent properties, but they are hard to adhere for the surface lacking of polarity. So low-pressure glow discharge of air plasma was used to improve the adhesion properties of wood/PE composites. The composites were treated by plasma under different discharge power. And the changes on the surface properties of the treated and untreated composites were studied by contact angle, Fourier transform infrared spectroscopy (FTIR), scanning electron microscope (SEM), atomic force microscope (AFM) and X-ray photoelectron spectroscopy (XPS) analysis. The measurement showed that the contact angle decreased after plasma treatment, and the contact angle decreased gradually with the increasing of discharge power. The FTIR analysis results showed that the polar groups such as hydroxyl, carbonyl and carboxyl were formed on the surface of the composites treated under plasma. SEM and AFM results showed that the roughness of plasma treated samples increased. XPS analysis results indicated that the content of carbon element decreased while the content of oxygen element in the composition of wood/PE composites surface element increased and it reached a balance in a higher power, meanwhile a lot of carboxyl groups were formed. The newly formed polar groups are benefit for the adhesion of composites. The shear bonding strength test showed that the adhesion properties of wood/PE composites improved effectively after plasma treatment.     

High pressure impedance spectroscopy of SrF2 nanocrystals

The charge transport behavior of strontium fluoride nanocrystals has been investigated by in situ impedance measurement up to 41?GPa. It was found that the parameters changed discontinuously at each phase transition. The charge carriers in SrF₂ nanocrystals include both F^? ions and electrons. Pressure makes the electronic transport more difficult. The defects at grains dominate the electronic transport process. Pressure could make the charge–discharge processes in the Fm3m and Pnma phases more difficult.     

Silver-coated LiVPO4F composite with improved electrochemical performance as cathode material for lithium-ion batteries

Nano-structured LiVPO₄F/Ag composite cathode material has been successfully synthesized via a sol–gel route. The structural and physical properties, as well as the electrochemical performance of the material are compared with those of the pristine LiVPO₄F. X-ray diffraction (XRD) and scanning electron microscopy (SEM) reveal that Ag particles are uniformly dispersed on the surface of LiVPO₄F without destroying the crystal structure of the bulk material. An analysis of the electrochemical measurements show that the Ag-modified LiVPO₄F material exhibits high discharge capacity, good cycle performance (108.5 mAh g⁻¹ after 50th cycles at 0.1 C, 93% of initial discharge capacity) and excellent rate behavior (81.8 mAh g⁻¹ for initial discharge capacity at 5 C). The electrochemical impedance spectroscopy (EIS) results reveal that the adding of Ag decreases the charge-transfer resistance (R_ct) of LiVPO₄F cathode. This study demonstrates that Ag-coating is a promising way to improve the electrochemical performance of the pristine LiVPO₄F for lithium-ion batteries cathode material.     

Improved performance of porous LiFePO4/C as lithium battery cathode processed by high energy milling comparison with conventional ball milling

Porous LiFePO₄ is synthesized and coated with amorphous carbon by using high energy nano-mill (HENM) processed solid-state reaction method. FeCl₃ (38%) containing water solution which is originated from pickling of steel scrap (waste liquid) is used as a source material in this study. The result indicates that LiFePO₄ powders are well coated with the amorphous carbon. HENM process successfully produces the porous LiFePO₄ with homogeneously distributed pores and a well networked carbon web, which delivers an enhanced electrochemical rate capability. HENM process is incorporated as an effective route for reducing particle size, distributing particle homogeneously and averting agglomeration of particles of precursor in this study. X-ray diffraction, scanning electron microscopy with elemental mapping, transmission electron microscopy with selected area (electron) diffraction, Raman spectroscopy, cyclic voltammetry, and galvanostatic charge/discharge are employed to characterize the final product. Electrochemical measurement shows that the synthesized LiFePO₄/C composite cathode delivers an initial discharge capacity of 161 mAhg⁻¹ at 0.1C-rate between 4.2 and 2.5 V. Remarkably, the cathode delivers 101.9 mAhg⁻¹ at high charge/discharge rate (10 C).     

Silver-coated graphene electrode produced by electrolytic deposition for electrochemical behaviors

This study evaluates the excellent electrochemical performance of silver (Ag)-coated graphene electrode using an electrolytic deposition technique. Ag particles are introduced to the graphene surface as a function of the applied current. A half cell of the Ag-coated graphene electrode is fabricated to examine the electrochemical performance, such as the charge–discharge behaviors, cyclic voltammetry, and specific capacitance. As a result, the electrochemical performance of the Ag-coated graphene electrode is two times higher than that of the crude graphene electrode.     

局域热力学平衡态空气电弧等离子体输运参数计算研究

空气电弧等离子体的物性参数为空气电弧放电过程的仿真提供了可靠的微观理论基础和参数输入. 假定体系处于局域热力学平衡态, 基于Chapman-Enskog理论, 采用Sonine多项式三级展开(对黏滞系数采用二级展开) 得到的输运参数表达式, 数值计算得到了不同气压条件下(0.1 atm-20 atm, 1 atm = 1.01325×10⁵ Pa)、 不同温度范围内(300-30000 K) 空气电弧等离子体的输运参数(扩散系数、黏滞系数、热导率、电导率). 与以往的理论研究相比, 最新的相互作用势和碰撞截面研究成果被应用到涉及粒子的碰撞积分计算中, 提高了输运参数计算结果的精度和可靠性.     

Charge transport and discharge mechanism in (PVC+KClO3) polymer electrolyte films

This paper presents results of the studies on ionic conductivity and transference number measurements on potassium chlorate (KClO₃) complexed polyvinyl chloride (PVC) films prepared by solution-cast technique. Temperature dependence of ionic conductivity and transference number data indicated the dominance of ion-type charge transport in these specimens. The magnitude of conductivity increased with increase in the concentration of the salt and temperature. Using this (PVC+KClO₃) electrolyte, solid-state electrochemical cells were fabricated and their discharge profiles were studied under a constant load of 100 kΩ. Several cell profiles associated with these cells were evaluated and are reported.