Analysis,design and simulation of MIM plasmonic filters with different geometries for technical parameters improvement

In this paper, four optical filter topologies based on metal–insulator–metal waveguides are proposed and the designed structures are investigated numerically using finite-difference timedomain method. Triangular-shaped adjunctions have been added to the filter structures to improve their transmission spectrum. These improved structures consist of air as the insulator and silver as the metal. The relative permittivity of metal has been described via the Drude,Drude–Lorentz, and Palik models. The first filter's transmission spectrum shows an acceptable transmittance. In the second optimized filter, the transmission spectrum has been improved. The transmittance spectrum can be tuned through adjusting the edge of the triangle in these four optimized filters. As a result, the bandwidths of resonance spectra can be adjusted. The theory of such tapered structures will be investigated by the tapered transmission line and will be solved with the transfer matrix method. This method shows a better performance and higher transmission efficiency in comparison with the basic structures. On the other hand, the final filter has been chosen as the best one because of its hexagonal resonator. The main reason for having a better result is due to a longer interaction length in comparison with the circular resonator. This in turn creates much better energy coupling and results in higher transmission.     

分子印迹膜的制备研究进展

将分子印迹技术与膜分离技术相结合的分子印迹膜,由于其高选择性,近年来受到了国内外研究者的广泛关注.本文初步探讨了分子印迹膜(MIM) 的两种分离机理以及目前主要的制备方法:同步法和复合法.     

新型荧光分子印迹膜特异性识别和检测目标蛋白质

制备了一种新型荧光分子印迹膜(L-半胱氨酸修饰的量子点嵌入的分子印迹膜(QDs@MIM)),并将其作为荧光人工受体用于目标蛋白质(溶菌酶)的特异性识别和检测。QDs@MIM以溶菌酶为模板分子、丙烯酰胺为功能单体、L-半胱氨酸修饰的量子点为辅助单体、N,N′-亚甲基双丙烯酰胺为交联剂,在预硅烷化的玻璃板上制备而成。在最佳条件下,QDs@MIM对溶菌酶检测的线性范围为0.1~1.0μmol/L,吸附平衡时间为4 min,选择性因子为6.2。该方法操作简单、吸附平衡时间短、选择性高,具备作为生物传感器快速分析样品中目标蛋白质的潜力。     

声表面波MIM隧道发光二极管

我们在研究MIM隧道发光结(金属-绝缘层-金属)的过程中,首次以表面声波代替表面随机粗糙度的作用,将MIM结制作在声表面波场中,结果使结的发光效率、发光强度、稳定性、均匀性都有改善.本文介绍了结的基本结构,基本工艺,阐明了结的发光机理,讨论了结的Ⅰ-Ⅴ特性曲线和光谱曲线,根据结具有显著的负阻现象,我们设计出了一种新型的开关器件.     

Cures for expansion shock and shock instability of Roe scheme based on momentum interpolation mechanism

The common defects of the Roe scheme are the non-physical expansion shock and shock instability. By removing the momentum interpolation mechanism (MIM), an improved method with several advantages has been presented to suppress the shock instability. However, it cannot prevent the expansion shock and is incompatible with the traditional curing method for expansion shock. To solve the problem, the traditional curing mechanism is analyzed. Effectiveness of the traditional curing method is discussed, and several defects are identified, one of which leads to incompatibility between curing shock instability and expansion shock. Consequently, an improved Roe scheme is proposed, which is with low computational costs, concise, easy to implement, and robust. More importantly, the proposed scheme can simultaneously solve the problem of shock instability and expansion shock without additional costs.     

Design of a sector bowtie nano-rectenna for optical power and infrared detection

We designed a sector bowtie nanoantenna integrated with a rectifier (Au−TiO_x−Ti diode) for collecting infrared energy. The optical performance of the metallic bowtie nanoantenna was numerically investigated at infrared frequencies (5−30 μm) using three-dimensional frequency-domain electromagnetic field calculation software based on the finite element method. The simulation results indicate that the resonance wavelength and local field enhancement are greatly affected by the shape and size of the bowtie nanoantenna, as well as the relative permittivity and conductivity of the dielectric layer. The output current of the rectified nano-rectenna is substantially at nanoampere magnitude with an electric field intensity of 1 V/m. Moreover, the power conversion efficiency for devices with three different substrates illustrates that a substrate with a larger refractive index yields a higher efficiency and longer infrared response wavelength. Consequently, the optimized structure can provide theoretical support for the design of novel optical rectennas and fabrication of optoelectronic devices.     

相容的聚甲基丙烯酸甲酯/[C12 MIM][PF6]离子液体体系在超临界CO2中的发泡性能

通过快速卸压法, 以超临界CO2为物理发泡剂, 研究了相容的聚甲基丙烯酸甲酯(PMMA)/1-n-十二烷基-3-甲基咪唑六氟磷酸盐([C12 MIM][PF6])离子液体(IL)复合体系的发泡性能. 加入IL后, PMMA对CO2的吸收量增加; 复合体系的玻璃化转变温度(Tg)随IL含量的增加而降低. IL对PMMA发泡行为的影响取决于发泡条件. 在较低温度和压力下, 纯PMMA无法发泡, IL的加入可促进泡孔形成; 提高温度和压力, 纯PMMA可以发泡, IL的加入在提高泡孔尺寸的同时使泡孔仍然保持尺寸分布均匀的微米级结构.     

[C14MIM]Br离子液体对聚丙烯超临界CO2发泡性能的影响

本文对PP/[C₁₄MIM]Br体系的熔融过程和对CO₂的吸收, 以及[C₁₄MIM]Br在PP基体中的分散状态进行了研究, 并初步考察了[C₁₄MIM]Br对PP发泡性能的影响.     

MIM结构的SPP模式理论与仿真计算研究

为了进一步明确MIM （Metal-insulator-metal）波导结构的SPP （Surface plasmon polariton）模式特性,建立了MIM结构的SPP模式关系、激发系数和反射系数的理论模型。仿真数值计算结果表明：较大的介质厚度的TM基态模式衰减超过了振荡模式衰减,与传统的介质波导明显不同;TE模式表现为失真的介质光波导模式特性,其传播距离要远大于TM₀;MIM结构中腔的Q值随着长度增加而增大,表明了SPP反射受限;腔的品质因数改变与端面关系密切;MIM波导可以在具有更大Q值下确保光波更好地耦合成需要的SPP模式。     

What is the basic chromophore of a dye?

Taking the 4,5-diphenyl-substituted 2-dimethylamino-3-azacyclopentadienone (4) as an example its colour has been discussed in relation to different basic chromophores (parent chromophores). The parent chromophore can be defined either as the structure which has nearly the same absorption wavelength as the dye under consideration or as the substructure which is electronically most closely related to the dye. In the case of4 both considerations lead to different results. Based on the correlation diagram between the electronic states involved in the electronic excitation the long-wavelength absorption of4 is better understood in terms of the merocyanine parent chromophore than in terms of a betainic substructure, which should have the same colour as4 and is the parent chromophore according toKlessinger. This conclusion is drawn fromPPP configuration analysis of the wavefunctions of4 relative to different molecular substructures. The molecular geometry predicted by the geometry-optimized MINDO/3 and QCFF/Pi calculations provided additional arguments in favour of the cyclomerocyanine structure of4. In respect to the colour4 belongs to a new series of cyclic-conjugated chromophoric systems.