Improvement of dielectric tunability and loss tangent of (Ba,Sr)TiO3 thin films with K doping

Ba_0.6Sr_0.4TiO₃ thin films doped with K were deposited on Pt/Ti/SiO₂/Si substrates by chemical solution deposition method. The structure, surface morphology, and dielectric and tunable properties of Ba_0.6Sr_0.4TiO₃ thin films have been studied in detail. The K content in Ba_0.6Sr_0.4TiO₃ thin films has a strong influence on the material's properties including surface morphology, dielectric and tunable properties. It is found that the Curie temperature of K-doped Ba_0.6Sr_0.4TiO₃ films shifts to higher values compared with that of undoped Ba_0.6Sr_0.4TiO₃ thin films, which leads to a dielectric enhancement of K-doped Ba_0.6Sr_0.4TiO₃ films at room temperature. At the optimized content of 0.02 mol, the dielectric loss tangent is reduced significantly from 0.057 to 0.020. Meanwhile, the tunability is enhanced obviously from 26% to 48% at the measured frequency of 1 MHz and the maximum value of the figure of merit is 23.8. This suggests that such films have potential applications for tunable devices.     

大口径多层介质膜光栅衍射效率测量及其在制作工艺中的应用

多层介质膜光栅是高功率激光系统的关键光学元件.为了满足国内强激光系统的迫切需求, 在大口径多层介质膜光栅的研制过程中,建立了单波长自准直条件下的衍射效率测量方法及其误差分析. 结果表明误差主要由探测器的噪声和测试人员的差异产生,对衍射效率测试精度的影响是±1%. 在此基础上,将光栅衍射效率及其分布测量技术应用于光栅制作工艺中, 作为大口径光栅无损检测的一种手段,如判断光栅掩模是否能进行离子束刻蚀、 离子束刻蚀的在线监测和是否需要再刻蚀,从而实现对大口径多层介质膜光栅离子束刻蚀过程的定量、 科学控制,提高了离子束刻蚀光栅制作工艺的成功率.利用上述技术,已成功研制出多块最大尺寸为 430 mm× 350 mm、线密度1740线/mm、平均衍射效率大于95%的多层介质膜光栅. 实验结果表明,该方法操作简单、测量快速准确,不必检测光栅微结构. 为大口径多层介质膜光栅研制的无损检测工程化奠定了基础.     

碳纤维复合材料内部缺陷深度的定量红外检测

利用脉冲红外热成像技术对碳纤维复合材料试件内部的模拟脱黏缺陷的深度进行测量, 研究在被测物热属性参数未知情况下,碳纤维增强塑料中缺陷深度的测量方法. 分析了平板材料在脉冲热源激励下的一维热传导模型;给出了内部缺陷深度的红外测量原理; 选用对数温度二阶微分峰值时刻作为特征时间测量缺陷深度; 考虑单点标定测量深度可能产生较大的随机误差,提出利用最小二乘法多项式拟合建立阶梯件中阶梯深度与其对应的对数温度时间二阶微分曲线峰值时间两者之间的标定关系式的方法, 选择在相对误差平方和最小情形下的拟合关系式作为脱黏缺陷深度测量的标定关系式. 实验结果表明,利用该方法测量脱黏缺陷深度的精度优于单点法标定测量结果, 实现了在被检测材料热属性参数未知的情况下仍能较准确地测量脱黏缺陷深度.     

卷绕式螺旋形薄膜介质脉冲形成线设计

采用模块化结构,设计了一种卷绕式螺旋形薄膜介质脉冲形成线,并且对绝缘材料、电极材料的选择依据进行了分析。基于模块化卷绕式脉冲形成线,研制的重复频率脉冲方波产生器采用4个开关同步触发四级形成线模块,从而实现多模块的电压串联叠加,以达到产生高压的目的。开关采用气体火花间隙开关,每级开关及充放电采用电感隔离。研制的脉冲产生器输出电压220 kV,脉冲宽度182 ns,前沿50 ns,可10 Hz重复频率稳定运行。     

亚微秒脉冲下高梯度绝缘子的沿面闪络特性

介绍了一种由聚酰亚胺和不锈钢叠加而成的高梯度绝缘子的实验研究工作。该绝缘子样品的直径60 mm,厚度8 mm,在脉冲宽度120 ns(FWHM)的电压脉冲加载下最高获得了接近13 MV/m的绝缘强度。研究了测试方法以及绝缘层厚度与金属层厚度的比例对高梯度绝缘子绝缘强度的影响,并与相同尺寸的普通材料绝缘子的绝缘强度进行了对比。结果表明,高梯度绝缘子的绝缘强度明显高于仅由聚酰亚胺构成的普通绝缘子。     

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.     

电介质桁架对频率选择表面传输特性的影响

为了分析电介质桁架结构对频率选择表面(FSS)传输特性的影响,以Y环单元的FSS和聚酰亚胺材质制备的桁架结构为例,采用时域有限差分方法进行计算和分析.建立物理模型并定义了孔径阻挡比P,通过分析证明了改变桁架的周期T以及肋骨的宽度D会对FSS的传输性能产生规律性影响,成为衡量电介质桁架结构的主要参数,且孔径阻挡比P的提高将增加传输损耗.当T值由无限大变为80 mm时,通带透过率平均下降超过0.9 dB;当D值由0变为20 mm时,通带透过率平均下降超过1 dB.当P值小于12.11%时通带不产生偏移现象;当P值小于4.12%时,桁架对FSS的影响可忽略不计.采用镀膜和光刻工艺制备FSS试件、数控机械加工方式制备电介质桁架,并在微波暗室中进行测量,验证实验与计算结果相符合,为拟采用电介质桁架结构的FSS隐身雷达罩工程应用提供了理论与实验的参考依据.     

大气压氦气介质阻挡放电倍周期分岔及混沌现象的实验验证

采用具有平行电极结构的介质阻挡放电装置,在大气压氦气条件下进行了一系列放电实验,观察了放电波形并对其进行了频谱分析.结果表明,在一定条件下随外施电压幅值的增加,大气压氦气均匀介质阻挡放电会由周期一态放电经周期二态、周期四态放电进入混沌态放电.研究验证了大气压氦气介质阻挡放电经倍周期分岔路径通向混沌的现象,不仅仅出现在数值仿真中,在现实实验中也是确实存在的.     

Effect of Polythiophene Content on Thermomechanical Properties of Electroconductive Composites

The thermal, mechanical and electrical properties of polymeric composites combined using polythiophene (PT) dopped by FeCl₃ and polyamide 6 (PA), in the aspect of conductive constructive elements for organic solar cells, depend on the molecular structure and morphology of materials as well as the method of preparing the species. This study was focused on disclosing the impact of the polythiophene content on properties of electrospun fibers. The elements for investigation were prepared using electrospinning applying two substrates. The study revealed the impact of the substrate on the conductive properties of composites. In this study composites exhibited good thermal stability, with T₅ values in the range of 230–268 °C that increased with increasing PT content. The prepared composites exhibited comparable PA T_g values, which indicates their suitability for processing. Instrumental analysis of polymers and composites was carried out using Fourier Transform Infrared spectroscopy (FT-IR), thermogravimetric analysis (TGA), differential scanning calorimetry (DSC), dynamic mechanical thermal analysis (DMTA) and scanning electron microscopy (SEM).     

Apparent Molar Volume, Heat Capacity, and Conductance of Lithium Bis(trifluoromethylsulfone)imide in Glymes and Other Aprotic Solvents

Lithium bis(trifluoromethylsulfone)imide (LiTFSI) is a promising electrolyte for high-energy lithium batteries due to its high solubility in most solvents and electrochemical stability. To characterize this electrolyte in solution, its conductance and apparent molar volume and heat capacity were measured over a wide range of concentration in glymes, tetraethylsulfamide (TESA), acetonitrile, -butyrolactone, and propylene carbonate at 25°C and were compared with those of LiClO₄ in the same solvents. The glymes or n(ethylene glycol) dimethyl ethers (nEGDME), which have the chemical structure CH₃–O–(CH₂–CH₂–O) _n –CH₃ for n = 1 to 4, are particularly interesting since they are electrochemically stable, have a good redox window, and are analogs of the polyethylene oxides used in polymer-electrolyte batteries. TESA is a good plasticizer for polymer-electrolyte batteries. Whenever required, the following properties of the pure solvents were measured: compressibilities, expansibilities, temperature and pressure dependences of the dielectric constant, acceptor number, and donor number. These data were used in particular to calculate the limiting Debye-Hückel parameters for volumes and heat capacities. The infinite dilution properties of LiTFSI are quite similar to those of other lithium salts. At low concentrations, LiTFSI is strongly associated in the glymes and moderately associated in TESA. At intermediate concentrations, the thermodynamic data suggests that a stable solvate of LiTFSI in EGDME exists in the solution state. At high concentrations, the thermodynamic properties of the two lithium salts approach those of the molten salts. These salts have a reasonably high specific conductivity in most of the solvents. This suggests that the conductance of ions at high concentration in solvents of low dielectric constant is due to a charge transfer process rather than to the migration of free ions.