A low specific on-resistance SOI MOSFET with dual gates and a recessed drain

A low specific on-resistance(Ron,sp) integrable silicon-on-insulator(SOI) metal-oxide semiconductor field-effect transistor(MOSFET) is proposed and investigated by simulation.The MOSFET features a recessed drain as well as dual gates,which consist of a planar gate and a trench gate extended to the buried oxide layer(BOX)(DGRD MOSFET).First,the dual gates form dual conduction channels,and the extended trench gate also acts as a field plate to improve the electric field distribution.Second,the combination of the trench gate and the recessed drain widens the vertical conduction area and shortens the current path.Third,the P-type top layer not only enhances the drift doping concentration but also modulates the surface electric field distributions.All of these sharply reduce Ron,sp and maintain a high breakdown voltage(BV).The BV of 233 V and Ron,sp of 4.151 mΩ·cm2(VGS = 15 V) are obtained for the DGRD MOSFET with 15-μm half-cell pitch.Compared with the trench gate SOI MOSFET and the conventional MOSFET,Ron,sp of the DGRD MOSFET decreases by 36% and 33% with the same BV,respectively.The trench gate extended to the BOX synchronously acts as a dielectric isolation trench,simplifying the fabrication processes.     

Hydrothermal synthesis of LiMnO2 microcubes for lithium ion battery application

Two kinds of LiMnO₂ microcubes were successfully synthesized by hydrothermal method using solid or hollow Mn₂O₃ microcubes as precursors. One was made up of nanoparticles varying in size and the other was made up of interlaced polygonal nanoplates with the thickness of 70 nm. Both kinds of LiMnO₂ microcubes were characterized by X-ray diffraction, scanning electron microscopy, and transmission electron microscopy. Charge–discharge curves were carried out to investigate their electrochemical properties. LiMnO₂ microcubes with interlaced nanoplates showed much better capacities than the ones with nanoparticles indicating it is more suitable for application in the lithium ion batteries. The former material could deliver the capacities of 197 and 134 mAh/g at 0.1 and 1 C, respectively. And its capacity fading after 50 cycles did not exceed 7 %. The excellent electrochemical performance of the former material could be ascribed to the smaller size which could shorten the path length for lithium ion transport and increase the electrode and electrolyte contact.     

Enhanced electrocatalytic oxidation of hydroxylamine on Pt/polypyrrole composite modified glassy carbon electrode

A sensitive hydroxylamine sensor is developed by electrodeposition of Pt nanoparticles on pre-synthesized polypyrrole nanoparticles modified glassy carbon electrode. The modified electrode presents distinctly electrocatalytic activity toward hydroxylamine oxidation. The kinetic parameters such as the overall numbers of electrons involved in hydroxylamine oxidation, the electron transfer coefficient, standard heterogeneous rate constant, and diffusion coefficient are evaluated. The current response increases linearly with increasing hydroxylamine concentrations and exhibits two wide linear ranges of 5.0?×?10^?7–1.1?×?10^?3 and 1.1?×?10^?3–18.8?×?10^?3 M with a detection limit of 0.08 μM (s/n?=?3). The proposed electrode presents excellent operational and storage ability for determining hydroxylamine. Moreover, the sensor shows good sensitivity, selectivity, and reproducibility properties.     

Immunoassays Based on Surface-Enhanced Fluorescence using Gap-Plasmon-Tunable Ag Bilayer Nanoparticle Films

A novel gap-plasmon-tunable Ag bilayer nanoparticle film for immunoassays is demonstrated. Different from a traditional Ag monolayer nanoparticle film, a desired number of polyelectrolyte (PEL) layers are deposited on the nanoparticles before the self-assembly of a second Ag nanoparticle layer. Interestingly, by controlling the number of the PEL interlayers, the gap plasmon between the two Ag nanoparticle layers can be tuned across the visible spectral range. The ability of the presented Ag bilayer nanoparticle films in fluorescence enhancement has been examined experimentally. A maximal enhancement of around 15.4 fold was achieved when 7 layers of polyelectrolyte were used. When this optimal Ag bilayer nanoparticle film was applied to fluorescence immunoassay, a performance with approximately 3.3-fold enhancement was obtained compared with that performed on a traditional glass substrate. The experimental results suggest that the presented gap-plasmon tunable Ag bilayer nanoparticle films have great potential in fluorescence-based immunoassays. The method of the bilayer-film construction presented here also provides new insights into the rational design of the plasmonic substrates.     

大电流碳纳米管场发射阴极研究

报道了在较大发射面积上获得较大场发射电流的碳纳米管场发射阴极。为了加强场发射电流,在丝网印刷浆料中增加一种金属纳米颗粒,金属颗粒增强了碳纳米管发射体和衬底的接触,提高碳纳米管和衬底的粘附作用。利用改进后的丝网印刷方法制备了大电流碳纳米管场发射阴极,测得最大发射电流为68.0 mA,阴极有效发射面积约1.1 mm2,发射电流密度约6.2 A/cm2;并成功将改进方法制备的大电流场发射碳纳米管阴极应用于场发射真空器件原型。实验证明这种具有较大发射电流和较大发射电流密度的场发射能够满足部分大功率电子器件的需求。收稿日期:; 修订日期:     

回旋加速器束测探头感生放射性实验研究

基于束流沉积法测量回旋加速器内部束流参数将在束测探头上产生感生放射性污染,从而对加速器调束工作人员带来不必要的辐射危害。采用AGM-6型监测仪对探头感生放射性进行在线测量,通过测量不同半径处探头受辐射后的空气比释动能率,间接反映探头感生放射性的强弱和危害。研究结果表明,在束流调试实验中,应尽量降低馈入高频的占空比;探头测量后冷却2~3 h取出,则不需要考虑测量探头辐照后的残留感生放射性的危害。     

矿井瞬变电磁精细探查技术在铁矿防治水中的应用

在铁矿开采过程中,经常会遇到断层破碎带、软弱夹层及含水异常体等不可直接预测的不良地质构造,不及时预测及治理将影响安全生产.在诸多的预测方法中物探技术以其无损、准确、高效、快捷而得到认可.其中,矿井瞬变电磁对存在视电阻率差异的岩性响应明显,其探测结果能准确区别岩性电性变化界面,在很多煤矿防治水工程中得到了印证.本文在简单介绍矿井瞬变电磁基本原理及精细探测技术的基础上,结合大牛铁矿实际地质情况,通过具体的探测实例的尝试,阐述了矿井瞬变电磁精细探测技术在铁矿防治水中的作用.     

基于多元高斯声束模型的圆柱体超声检测声场仿真

为了提高圆柱体缺陷检测的准确性,需了解其超声声场分布。针对圆柱体实际检测的要求,本文采用超声水浸检测法。通过多元高斯声束模型分别模拟了实心圆柱体及空心圆柱体中的辐射声场,计算仿真了垂直入射与倾斜入射至圆柱体时的声场,实现了检测声场的可视化。通过计算得出仿真结构与实际理论相符,表明本论文的方法能够应用在圆柱体结构超声声场仿真中。     

Experimental study of the temperature and electron-irradiation effect on erbium-doped fiber amplifiers

We study the influence of temperature on the gain of 980 nm pumped erbium-doped fiber amplifier (EDFA) before and after the electron irradiation. Our experimental results indicate that in the irradiation process the EDFA gain at low temperatures is less than that at high temperatures, but after 7 days recovery, the EDFA gain at low temperatures is significantly higher than that at high temperatures. After 200 krad electron irradiation, the EDFA gain is more sensitive to temperature as compared to non-irradiated one.