玻纤增强复合材料冲击Hugoniot参数实验研究

在单级轻气炮上,对一种玻纤增强复合材料的冲击Hugoniot参数进行了实验研究。最高撞击速度为520 m/s,相应在靶中得到的最高撞击压力为2.815 GPa.压力测试采用锰铜计,PVDF产生的压电信号用于判读激波速度。由实验结果拟合得到了玻纤增强复合材料的Hugoniot线性关系和Grüneisen系数。     

红外制导技术在精确打击武器中的应用

红外制导技术利用红外探测器捕获和跟踪目标自身辐射的能量来实现寻的制导,具有制导精度高、不受无线电干扰影响及可昼夜作战的特点。归纳了红外制导技术的特点,介绍了该技术在国内外发展的历程,对红外制导技术在精确打击武器中应用的几个关键问题和发展趋势进行了分析。结果表明,红外探测器正朝着小型化、高分辨率、高灵敏度化方向发展;随着红外图像与可见光图像的匹配与融合技术以及复合制导技术的发展,工作频段的选择、气动光学效应和成像条件的影响以及如何更好地评价融合效果是目前亟待解决的问题。     

3种多层复合防护板抗破片侵彻试验研究

为指导高动能破片防护结构优化设计,通过模拟破片侵彻试验,对3种多层复合防护结构进行防护性能对比研究,并简要分析不同结构的防护机理。结果表明,在试验对比的结构中,陶瓷/钢/FRP复合结构对高动能破片的侵彻防护性能最佳。     

Enhanced carrier mobility and photon-harvesting property by introducing Au nano-particles in bulk heterojunction photovoltaic cells

In this study, polymer solar cells (PSCs) doped with Au nanoparticles (Au NPs) were successfully fabricated to maximize the photon-harvesting properties on the photoactive layer. In addition, a conductivity-enhanced hybrid buffer layer was introduced to improve the photon absorption properties and effectively separate the generated charges by adding Au NPs and dimethylsulfoxide (DMSO) to the PH 500 as a buffer layer. The PSC performance was optimized with a 88% improvement over the conventional PSCs (photoactive area: 225 mm², power conversion efficiency (PCE): 3.2%) by the introduction to the buffer layer of Au NPs and DMSO at 10 wt% and 1.0 wt%, respectively, and with 15 wt% Au NP doping in the photoactive layer. The internal resistance was decreased due to the increased photocurrent caused by the localized surface plasmon resonance (LSPR) effect of the Au NPs in the photoactive layer and by the improvement of carrier mobility induced by the DMSO doping of the buffer layer. As a result, the series resistance (R_S) deceased from 42.3 to 19.7 Ω cm² while the shunt resistance (R_SH) increased from 339 to 487 Ω cm².     

纳米钛粉改性环氧底漆对GFEP飞机电磁屏蔽性能的影响

航空电子设备的发展和地面电磁波源的迅速增多对玻璃纤维增强环氧树脂(GFEP)机身结构飞机的运行安全构成了威胁,亟需提升此类机身结构的电磁屏蔽性能。介绍了电磁屏蔽效能的计算方法,提出了在GFEP飞机机身涂覆纳米钛粉改性环氧底漆的应对方案。制备了纳米钛粉质量分数为1.0%的改性环氧底漆,研究了改性底漆对GFEP飞机机身典型结构样品电磁屏蔽性能的影响。结果表明:在300 kHz~1.5 GHz的测试范围内,涂覆改性底漆的测试样品的电磁屏蔽效能良好,达到9.5~29.7 dB。     

Alcohol soluble titanium(IV) oxide bis(2,4-pentanedionate) as electron collection layer for efficient inverted polymer solar cells

We demonstrate efficient inverted polymer solar cells (PSCs) based on poly(3-hexylthiophene) (P3HT) and [6,6]-phenyl-C₆₁-butyric acid methyl ester (PCBM) by using solution-processed titanium(IV) oxide bis(2,4-pentanedionate) (TOPD) as electron collection layer (ECL) between the indium tin oxide (ITO) electrode and photoactive layer. The TOPD buffer layer was prepared by spin-coating isopropanol solution of TOPD on ITO and then baked at 140 °C for 5 min. The power conversion efficiency (PCE) of the inverted PSC with TOPD buffer layer reaches 4% under the illumination of AM1.5G, 100 mW/cm², which is increased by 76% in comparison with that (2.27%) of the inverted device without TOPD ECL. The results indicate that TOPD is a promising electron collection layer for inverted PSCs.     

Improving the performance of polymer solar cells by altering polymer side chains and optimizing film morphologies

Two donor–acceptor (D–A) type conjugated polymers using dodecyl- and ethylhexyl-thiophene substituted benzo[1,2-b:4,5-b′]dithiophene (BDT-DDT and BDT-EHT, respectively) as donors and n-alkylthieno[3,4-c]pyrrole-4,6-dione (TPD) as acceptor were synthesized and characterized. The thiophene substituted BDT unit was recognized as a two-dimensional (2D) π-extended segment with high carrier mobility and TPD unit was a relatively strong electron-drawing acceptor, which could lead to deep-lying highest occupied molecular orbital (HOMO) levels of the polymers. The optical properties, electrochemical behavior, and charge carrier properties of the polymers were compared in parallel. The results indicated that ethylhexyl-substitution could optimize the polymer structures and properties. The bulk-heterojunction polymer solar cells (PSCs) based on the two polymers were fabricated and characterized. The devices based on ethylhexyl-substituted polymer showed better performance than that of dodecyl-substituted one. Further analysis proved that the improvement was mainly ascribed to the formation of well-defined nanostructures by using branched ethylhexyl side chains, which facilitated charge separation and transport in the bicontinous active layer. This study suggests that obtaining appropriate film morphology and phase separation by altering alkyl side chains is extraordinary important for high performance PSCs based on D–A type polymers.     

New antenna design approach – 3D polymer printing and metallization. experimental test at 14–18 GHz

This paper proves a new approach for rapid prototyping of radio antennas through 3D printing and chemical metallization. For this purpose, a standard metal pyramidal horn prototype is compared with its 3D printed replica. Three different 3D polymer printers are tested. The printed samples are assessed nondestructively by an X-ray Industrial Computed Tomography (CT) scanner, and then metalized via chemical deposition and chemical-electrochemical deposition. Copper with two different layer thicknesses and nickel materials are deployed and verified as a metallization opportunity. Again the CT scanner, X-ray fluorescent analysis and nanoindentation technique were used to perform the metallization quality estimation. As a result, a qualitative polymer prototype was produced having weight of 13 g – ten times lighter than the original. The prototype was successfully metalized and was able to be soldered. The radio-measurement comparison with the metal original for frequencies 14–18 GHz showed no significant differences. Finally, a simple dynamometric test confirmed the bonding between the metal and the polymer. To the best of our knowledge this is the first known comprehensive analysis of the possibility to print 3D lightweight wideband polymer antenna prototypes with a stable chemical metallization and radio properties very close to the original at 14–18 GHz.     

Improved performance of deep-blue polymer light-emitting diodes by one-step coating self-assembly hole injection/transport nanocomposites with both the optical and electrical optimization

In this study we demonstrate an easy solution-processed highly efficient deep-blue polymer light-emitting diode (PLED) via a simple one-step coating of self-assembly hole injection/transport nanocomposites to achieve both a finer hole ohmic contact and an increased light outcoupling, which is the first time report about both the optical and electrical optimization without necessitating changes in the design or structure of the wide bandgap deep-blue PLEDs themselves. The contact angle and surface energy measurement results demonstrate that triazine-based hole injection molecules can vertically migrate towards the bottom PEDOT:PSS layer to obtain a stable minimum of free energy, resulting in an optimal top-to-bottom HOMO energy level arrangement and an improved hole mobility in deep-blue PLEDs. The random surface nanostructure was formed on top of the hole bilayer, leading to the enhancement of light outcoupling verified by transmittance, transmittance haze and light extraction efficiency. Furthermore, in order to explore the reasons of the hole light scattering formation process, a transient drying monitoring technique is applied to track the drying process of the nanostructure films, revealing this approach effectiveness by easily modifying mixing ratios for obtaining different light outcoupling abilities.