Anodic oxidation of anthraquinone dye Alizarin Red S at Ti/BDD electrodes

The boron-doped diamond (BDD) thin-film electrode with high quality using industrially titanium plate (Ti/BDD) as substrate has been prepared and firstly used in the oxidation of anthraquinone dye Alizarin Red S (ARS) in wastewaters. The Ti/BDD electrodes are shown to have high concentration of sp³-bonded carbon and wide electrochemical window. The results of the cyclic voltammetries show that BDD has unique properties such as high anodic stability and the production of active intermediates at the high potential. The oxidation regions of ARS and water are significantly separated at the Ti/BDD electrode, and the peak current increases linearly with increasing ARS concentration. The bulk electrolysis shows that removal of chemical oxygen demand (COD) and color can be completely reached and the electrooxidation of ARS behaves as a mass-transfer-controlled process at the Ti/BDD electrode. It is demonstrated that the performances of the Ti/BDD electrode for anodic oxidation ARS have been significantly improved with respect to the traditional electrodes.     

Hydrogen and oxygen plasma enhancement in the Cu electrodeposition and consolidation processes on BDD electrode applied to nitrate reduction

Copper nanoparticle electrodeposition and consolidation processes were studied on boron doped diamond (BDD) electrode submitted to hydrogen and oxygen plasma treatments. The modified BDD films were applied as electrodes for nitrate electroreduction. The results showed that both treatments have a strong influence on the copper deposition and dissolution processes. For BDD treated with hydrogen plasma the copper electrodeposit was homogeneous with high particle density. This behavior was attributed to the BDD surface hydrogenation that improved its conductivity. On the other hand, the treatment with oxygen plasma was important for the copper nanoparticle consolidation on BDD surface, confirmed by the result's reproducibility for nitrate reduction. This performance may be associated with the formation of oxygen groups that can act as anchor points for Cu-clusters, enhancing the interfacial adhesion between diamond and the metal coating. The best electrochemical nitrate reduction response was obtained in acid media, where occurred the separation of the nitrate reduction process and the water reduction reaction.     

One model of electric conduction and electric field distributions in a liquid insulator

The electric properties of the liquid insulator have been studied in this work. We have described the time-dependent model of the conduction processes in the liquid insulator under high voltages. Our model is a generalization of the Frenkel conduction model. (The last deals only with stationary conduction processes). Calculation of the electric field has also been made for two types of problems: (1) the external electric field applied to a liquid, is created by plane electrodes. (2) A spherical electrode of a small size creates it. The electrodes are assumed to be under constant high voltage. There is no electron emission or ion injection from the electrodes. But the field intensity influences on the molecular dissociation rate, and this fact has been taken into account. We have shown that the space charge, which arises under conditions mentioned above gives rise to changes in the electric field distribution. The model on hand is also used for calculating the hydrodynamic phenomena under high non-uniform electric field intensities. It has also been shown that the velocity of the strong EHD flows is proportional to the value of direct current or the squared value of applied voltage.     

应用双面电极的PLZT横向电光调制器电场的精确解

使用保角变换方法导出了横向电光调制器中双面电极结构的电场和电容的解析表达式，给出了用于ＰＬＺＴ电光陶瓷介质中二次电光效应分析的电场分布的物理图像。通过计算对比表明，双面电极结构电极边级区域由于过剩双折射引起的强度调制非均匀性较单面电极有所改善。     

纳秒脉冲电压同轴电场下有机玻璃和尼龙的闪络特性

 利用基于SOS的SPG200高压脉冲功率装置研究了有机玻璃(PMMA)和尼龙1010在变压器油中的闪络特性。研究结果表明：闪络电压随内电极直径增加近似指数增加，随闪络距离延长近似线性增加，相应的击穿时延也近似线性增加。受实验条件的影响，有机玻璃和尼龙1010的闪络性能略有差异。同轴径向电场降落集中在内电极表面附近一定径向距离内，同轴电场下的闪络电压主要由内电极表面电场与径向电场分布的均匀程度决定。增加内电极直径和延长闪络距离都可以提高闪络电压，而增加内电极直径的效果更显著。     

TEA CO2激光器预电离结构电极系统的电场研究

 高功率气体激光器的非对称复杂电极系统中,电极参数的变化以及预电离结构的引入将会使所设计的均匀电场发生具体的改变。采用高精度有限元方法,对这类复杂电极系统进行建模并且计算其电场分布,根据分析结果更合理地指导激光器设计。对一种典型的非对称复杂电极系统TEA CO₂激光器,应用该方法并结合了预电离过程,研究了引入预电离器导体和变化电极形状对电极表面的电场强度起伏和放电空间的均匀电场面积产生的影响。结果表明:通过这种预先模拟,合理选择电极构型参数和预电离结构安装位置,可以产生性质较好的均匀电场以及效率较高的激光输出。     

Cathodic and anodic pre-treated boron doped diamond with different sp content: Morphological,structural, and impedance spectroscopy characterizations

In this work, the influence of cathodic (Red) and anodic (Ox) pre-treatment on boron doped diamond (BDD) films grown with different sp²/sp³ ratios was systematically studied. The sp²/sp³ ratios were controlled by the addition of CH₄ of 1,3,5 and 7 sccm in the gas inlet during the growth process. The electrodes were treated in 0.5 mol L⁻¹ H₂SO₄ at −3 and 3 V vs Ag/AgCl, respectively, for 30 min. The electrochemical response of BDD films was investigated using electrochemical impedance spectroscopy (EIS) and Mott–Schottky Plot (MSP) measurements. Four film sample sets were produced in a hot filament chemical vapor deposition reactor. During the growth process, an additional H₂ line passing through a bubbler containing the B₂O₃ dissolved in methanol was used to carry the boron. The scanning electron microscopy morphology showed well faced films with a small decrease in their grain size as the CH₄ concentration increased. The Raman spectra depicted a pronounced sp² band, mainly for films with 5 and 7 sccm of CH₄. MSP showed a decrease in the acceptor concentration as the CH₄ increased indicating the CH₄ influence on the doping process for Red–BDD and Ox–BDD samples. Nonetheless, an apparent increase in the acceptor concentrations for both Ox–BDD samples was observed compared to that for Red–BDD samples, mainly attributed to the surface conductive layer (SCL) formation after this strong oxidation process. The EIS Nyquist plots for Red–BDD showed a capacitance increase for the films with higher sp² content (5 and 7 sccm). On the other hand, the Nyquist plots for Ox–BDD can be described as semicircles near the origin, at high frequencies, where their charge transfer resistance strongly varied with the sp² increase in such films.     

The influence of boron content on electroanalytical detection of nitrate using BDD electrodes

Electrochemical response of nitrate reduction was analyzed using Boron Doped Diamond (BDD) films grown with different boron levels and it was correlated with the electrode physico-chemical properties. X-ray photoelectron spectroscopy and contact angle measurements showed the evolution of oxygen content and the weattability associated to the chemical surface modification as boron content increase in such films. Raman spectroscopy showed that the broad peaks at 1220 and 500 cm⁻¹ become more evident with the boron addition. Electrochemical measurements by square wave voltammetry for nitrate reduction showed a strong dependence between the doping level of the BDD film and the nitrate detection. BDD film grown with B/C ratio of 20,000 ppm presented the best sensibility to low concentration of nitrate. This result was analyzed from the linear relationship between the peak currents as a function of the nitrate concentration. This behavior was attributed to the changes in the diamond surface chemical and the film grain size.     

Influence of boron concentration on growth characteristic and electro-catalytic performance of boron-doped diamond electrodes prepared by direct current plasma chemical vapor deposition

A series of boron-doped diamond (BDD) electrodes were prepared by direct current plasma chemical vapor deposition (DC-PCVD) with different compositions of CH₄/H₂/B(OCH₃)₃ gas mixture. A maximum growth rate of 0.65 mg cm⁻² h⁻¹ was obtained with CH₄/H₂/B(OCH₃)₃ radio of 4/190/10 and this growth condition was also a turning point for discharge plasma stability which arose from the addition of B(OCH₃)₃ that changed electron energy distribution and influenced the plasma reaction. The surface coating structure and electro-catalytic performance of the BDD electrodes were characterized by scanning electron microscopy (SEM), X-ray diffraction (XRD), Raman spectroscopy, Hall test, and electrochemical measurement and electro-catalytic oxidation in phenol solution. It is suggested that the boron doping level and the thermal stress in the films are the main factors affecting the electro-catalytic characteristics of the electrodes. Low boron doping level with CH₄/H₂/B(OCH₃)₃ ratio of 4/199/1 decreased the films electrical conductivity and its electro-catalytic activity. When the carrier concentration in the films reached around 10²⁰ cm⁻³ with CH₄/H₂/B(OCH₃)₃ ratio over a range of 4/195/5-4/185/15, the thermal stress in the films was the key reason that influenced the electro-catalytic activity of the electrodes for its effect on diamond lattice expansion. Therefore, the BDD electrode with modest CH₄/H₂/B(OCH₃)₃ ratio of 4/190/10 possessed the best phenol removal efficiency.     

ITO界面调制层对GZO电极LED器件性能的影响

采用磁控溅射制备GZO和具有ITO界面调控层的GZO(ITO/GZO)透明导电薄膜作为大功率LED的电流扩散层,对比研究界面调控层对LED器件性能的影响。研究结果表明,ITO/GZO薄膜的透过率在可见光区达80%以上,退火后的ITO/GZO薄膜有较低的电阻率(1.15×10^-3 Ω·cm)。ITO调控层的介入能够调制GZO表面粗糙度,有利于改善LED外量子效率,降低GZO/p-GaN界面的接触势垒,提高LED器件的光电性 能。通过ITO界面调控后,LED器件20 mA驱动电流下的工作电压从9.5 V降低为6.8 V,发光强度从245 mcd 升到297 mcd,提高了20%;驱动电流为35 mA时,其发光强度从340.5 mcd 升到511 mcd,提高了50%。     

TEA CO2激光器非对称电极系统的电场分布

 设计了一种非对称电极,这种非对称电极的阳极是Chang电极或Ernst电极,阴极是由直线和圆弧构成的简单电极。通过比较和分析非对称电极和对称电极的特点发现,非对称电极系统中简单电极的边缘电场起伏最大。采用有限元方法计算了非对称电极系统中的简单电极取不同的直线长度和弧线半径时,非对称电极系统的电场分布,给出了选择非对称电极系统中的简单电极参数的依据。结果表明：这种非对称电极系统结合了解析电极和简单电极的优点,通过选择非对称电极系统的简单电极参数,它可以在TEA CO₂激光器中产生边缘电场起伏小于0.06,且满足电极表面均匀场面积宽度要求的电场。     

Application of BDD thin film electrode for electrochemical decomposition of heterogeneous aromatic compounds

The aim of the presented study is to investigate the applicability of electrochemical oxidation of aromatic compounds containing heteroatoms, e.g. waste from production of pesticides or pharmaceutics, at a borondoped diamond (BDD) electrode. The BDD electrodes were synthesized by microwave plasma enhanced chemical vapour deposition (MW PE CVD). Investigation of the electrode surface by optical microscopy and scanning electron microscopy (SEM) confirmed that the synthesized layer was continuous and formed a densely packed grain structure with an average roughness of less than 0:5 ??m. The influence of important electrochemical parameters: current density, kind of reactor, pH or mixing operation, on the efficiency of the oxidation was investigated. The fouling of electrode??s surface caused by the deposition of organic material was observed during CV and galvanostatic experiments. At low current density the oxidation rate constant k was low, but the current efficiency was relatively high. The BDD can be used successfully to remove heterogeneous aromatic compounds existing either as molecules or cations. During 4 h of electrolysis 95% of aromatic compounds were electrochemically decomposed to mineral forms. It was observed that the influence of the initial pH on mineralization was marginal.     

TEA CO2激光器均匀场电极的设计

介绍了与此有关的大面积均匀场放电电极的设计以及实验研究结果。无限大平行平板电极两极间的电场分布是均匀的,而现实的问题则是要求在有限的（电极）尺寸条件下实现电场的均匀性设计,因此设计问题转变为放电电极的剖面形状的理论和工程计算问题。根据TEA CO₂激光器工作的实际情况,有针对性地选择Chang氏理论作为设计依据。设计的放电电极实验结果证明,TEA CO2激光器在500HZ高重频脉冲条件下能够连续工作10分钟,在55mm放电电极宽和平坦部分为40mm剖面的平行平板两个主放电极之间实现了大面积稳定的均匀场辉光放电。     

外加磁场对射频磁控溅射制备铝掺杂氧化锌薄膜影响的研究

利用射频磁控溅射法制备了铝掺杂氧化锌(AZO)透明导电薄膜,在传统的磁控溅射系统中引入外加磁场,研究了外加磁场对AZO薄膜沉积速率、形貌结构及光电特性的影响.研究结果表明,外加磁场后薄膜的沉积速率从不加磁场的13.04 nm/min提高到了19.93 nm/min;外加磁场后薄膜表面平整致密、颗粒大小均匀,结晶质量较高,而不加磁场薄膜表面形貌呈蠕虫状,薄膜质量较差.溅射时间为90 min时,外加磁场前后AZO薄膜方阻分别为30.74?/和12.88?/.外加磁场对薄膜可见光透过率影响不大,但使薄膜的吸收边蓝移现象更明显.运用ansys软件对磁控溅射二维磁场分布模拟后发现,外加磁场提高了靶上方横向磁场强度,改善了磁场分布的均匀性,加强了磁场对电子的磁控作用,提高了靶电流,是AZO薄膜的溅射速率、光电性能和形貌结构得到提高和优化的原因.     

Uniformity analysis of dielectric barrier discharge (DBD) processed polyethylene terephthalate (PET) surface

A dielectric barrier discharge (DBD) plasma, operating in air at atmospheric pressure, has been used to induce changes in the surface properties of polyethylene terephthalate (PET) films. The effects that the key DBD operating parameters: discharge power, processing speed, processing duration, and electrode configurations, have on producing wettability changes in the PET surface region have been investigated. The approach taken involves the application of an Taguchi experimental design and robust analysis methodology. The various data sets obtained from these analyses have been used to studies the effect of the operating parameters on the surface uniformity and efficiency of the said treatment.In general, the results obtained indicate that DBD plasma processing is an effective method for the controlled surface modification of PET. Relatively short exposures to the atmospheric pressure discharge produces significant wettability changes at the polymer film surface, as indicted by pronounced reductions in the water contact angle measured. It was observed that the wettability of the resultant surface shows no significant differences in respect to orientation parallel (L-direction) or perpendicular (T-direction) to the electrode long axis. However, there was significant differences between the data obtained from these two orientations. Analysis of the role of each of the operating parameters concerned shows that they have a selective effectiveness with respect to resultant surface modification in terms of uniformity of modification and wettability. The number of treatment cycles and the electrode configuration used were found to have the most significant effects on the homogeneity of the resultant PET surface changes in L- and T-orientation, respectively. On the other hand, the applied power showed no significant role in this regard. The number of treatment cycles was found to be the dominant factor (at significance level of 0.05) in respect of water contact angle changes at the processed PET surface in both orientations. The driven metal electrodes (stainless steel or aluminium) were apparently superior to the driven dielectric electrode (ceramic or quartz) configurations. The grounded electrode in each case was a silicon rubber-covered aluminium plate (see later). The nature and scale of the surface changes that originate from the various processing conditions employed have been considered so as to determine the optimum treatment conditions in respect of processing outcomes, properties and any orientation dependence. Thus, it was revealed that higher processing speeds and longer processing durations are key for uniformity along the electrode axial orientation, while lower processing speeds and short exposure durations are key considerations, in the corresponding perpendicular orientation. In general, longer processing durations (low processing speeds and a high number of treatment cycles) and higher plasma powers induced greater changes in the surface wettability of the PET, as demonstrated by the observed water contact angles. This behaviour is taken to indicate that different combinations of DBD operating parameters and electrodes produce discharge conditions that can result in different plasma chemical processes in respect of uniformity, treatment efficiency and orientation dependence.     

Improved dielectric and electrical properties of (Ba,Sr)TiO3 thin films using Pt/LaNiO3 as the top-electrode material

(Ba,Sr)TiO₃ (BST) capacitors grown on a LaNiO₃ (LNO) bottom electrode, with Pt (80 nm), LNO (100 nm), and double-layer Pt/LNO (80/10 nm) top electrodes have been investigated. It was found that the dielectric behavior is improved by a decrease of the electrical properties for the BST capacitor using double-layer Pt/LNO top electrodes. The dielectric constant of 100 nm-thick BST films with a Pt electrode was only 165 at 100 kHz, while that with a double-layer electrode was about 242. Correspondingly, the tunability was greatly improved from 26% to 41% with an electric field of 600 kV/cm. These have been attributed to increased interfacial capacitance density, which resulted from an improved interface, between the films and the top electrode. The dielectric loss was also reduced by using a double-layer electrode. Furthermore, the leakage current of a capacitor with a double-layer Pt/LNO electrode was one order of magnitude lower than that with a single LNO electrode. It can be explained by the fact that the weak chemical interaction between LNO (10 nm) and BST causes a high potential barrier at the interface. PACS 81.15.-z; 81.15.Cd; 77.55.+f; 77.84.Dy; 77.22.-d     

迁移率对单层有机发光器件中电场与载流子分布的影响

有机发光器件的宏观特性与有机层中的电场和载流子浓度分布密切相关。建立的有机电致发光器件模型是由两个金属电极中间夹一层有机发光薄膜材料组成的单层器件,金属与有机发光层之间为欧姆接触。模型以载流子运动的扩散-漂移理论为基础,利用数值方法研究了有机发光层中双极载流子注入时的电势、电场、载流子浓度和复合密度分布。分析结果表明:当两种载流子的迁移率相同时,电场强度、载流子浓度、复合密度的分布呈对称形式。而当电子和空穴的迁移率μn和μp相差比较大时,高迁移率的载流子不仅仅分布在注入端附近而且还有一小部分能够传输到另一端,而低迁移率的载流子只分布在其注入端附近;当μn、μp的大小相差不大时,载流子传输情况就介于两者之间。当μn/μp的比值变化时,电场强度的极大值向载流子迁移率小的注入端偏移。     

JAEA 10A多峰源放电中电极布局模拟

采用自主研发的全三维PIC/MCC软件对JAEA 10A多峰负氢离子源进行系统仿真,分析了电极布局对H^-体积产生效率的影响。模拟结果显示：放电功率一定的情况下,增加电极数目,高能电子导致的横向漂移相对减弱,进而得到相对均匀的H^-束;但电子的相对利用率越低,导致H^-体积产生效率较低。电极越靠近过滤磁区,高能电子导致的横向漂移相对增强,H^-体积产生效率较低。改变电极数量,H^-体积产生效率和空间均匀性不可兼得,电极远离磁过滤区,可实现双赢。     

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采用自主研发的全三维PIC/MCC软件对JAEA 10A多峰负氢离子源进行系统仿真,分析了电极布局对H?体积产生效率的影响.模拟结果显示:放电功率一定的情况下,增加电极数目,高能电子导致的横向漂移相对减弱,进而得到相对均匀的H?束;但电子的相对利用率越低,导致H?体积产生效率较低.电极越靠近过滤磁区,高能电子导致的横向漂移相对增强,H?体积产生效率较低.改变电极数量,H?体积产生效率和空间均匀性不可兼得,电极远离磁过滤区,可实现双赢.     

Modeling of electrically actuated elastomer structures for electro-optical modulation

A transparent elastomer layer sandwiched between two metal electrodes deforms upon voltage application due to electrostatic forces. This structure can be used as tunable waveguide. We investigate structures of a polydimethylsiloxane (PDMS) layer with 1–30 μm thickness and 40 nm gold electrodes. For extended electrodes the effect size may be calculated analytically as a function of the Poisson ratio. A fully coupled finite-element method (FEM) is used for calculation of the position-dependent deformation in case of structured electrodes. Different geometries are compared concerning actuation effect size and homogeneity. Structuring of the top electrode results in high effect magnitude, but non-uniform deformation concentrated at the electrode edges. Structured bottom electrodes provide good compromise between effect size and homogeneity for electrode widths of 2.75 times the elastomer thickness.