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2010 International Conference on Enabling Science and Nanotechnology (ESciNano)最新文献

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Electrically conductive zinc oxide (ZnO) nanostructures prepared by solgel spin-coating 溶胶旋涂法制备导电氧化锌纳米结构
N. Sin, M. H. Mamat, M. Rusop, Z. Zulkifli
The electrically conductive zinc oxide (ZnO) nanostructures prepared by sol-gel spin coating are presented. This project has been focused on electrical, optical and structural properties of Al doped ZnO thin film. The effects of Al doping concentration at 0∼5 at.% on the Al doped ZnO thin film properties have been investigated. This project involves 3 processes which are thin film preparation, deposition and characterization. The thin films were characterized using Current-Voltage (I–V) measurement and UV-Vis-NIR spectrophotometer for electrical properties and optical properties respectively. The surface morphology has been characterized using field emission scanning electron microscope (FESEM). The I-V measurement result indicated electrical properties of Al doped ZnO thin film improved with Al doping. The absorption coefficient spectra obtained from UV-Vis-NIR spectrophotometer measurement show all films have low absorbance in visible and near infrared (IR) region but have high UV absorption properties. The FESEM investigations shows that the nanoparticles size become smaller and denser as the doping concentration increase.
介绍了溶胶-凝胶自旋镀膜法制备的导电氧化锌纳米结构。本项目主要研究Al掺杂ZnO薄膜的电学、光学和结构特性。Al掺杂浓度在0 ~ 5 at的影响。对Al掺杂ZnO薄膜性能的影响进行了研究。本项目涉及薄膜制备、沉积和表征3道工序。采用电流-电压(I-V)测量和紫外-可见-近红外分光光度计分别对薄膜的电学性能和光学性能进行了表征。利用场发射扫描电镜(FESEM)对其表面形貌进行了表征。I-V测量结果表明,Al掺杂ZnO薄膜的电学性能得到改善。紫外-可见-近红外分光光度计测量所得的吸收系数光谱表明,所有薄膜在可见光和近红外区域具有较低的吸光度,但具有较高的紫外吸收性能。FESEM研究表明,随着掺杂浓度的增加,纳米颗粒尺寸变小,密度增大。
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引用次数: 4
Single electron-hole pair generation using dark-bright solitons conversion control 利用暗-亮孤子转换控制产生单电子-空穴对
Pub Date : 2010-12-01 DOI: 10.1109/ESCINANO.2010.5700953
R. Jomtarak, C. Teeka, P. Yupapin, J. Ali
Recently, the electron-hole pair generated in 1.06-µm separate-absorber-avalanche (multiplier) InP-based devices [1], SiGe/Si planar waveguides [2] fabricated with a Ge concentration ranging from 2% to 6% and different thicknesses ranging from 200 nm to 2 µm, generating electron-hole pairs with a 100 fs laser pulse emitted at 810 nm, and monitoring the free-carrier absorption transient with a c.w. probe beam at 1.55 µm, bipolar transistors [3], CMOS process [4], InAs-GaSb superlattice (SL) photodiodes [5], resonant microcavity [6], A cavity-QED using a single InAs quantum dot and a high-Q whispering gallery mode [7].
最近,在1.06-µm分离吸收雪崩(倍增)inp器件中产生的电子空穴对[1]、在锗浓度为2% - 6%、厚度为200 - 2µm的SiGe/Si平面波导[2]、在810 nm发射100 fs激光脉冲时产生的电子空穴对、在1.55µm波长用c.w.探针束监测自由载流子吸收瞬态、双极晶体管[3]、CMOS工艺[4]、InAs- gasb超晶格(SL)光电二极管[5],谐振微腔[6],使用单个InAs量子点和高q低语廊模式的腔- qed[7]。
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引用次数: 0
Fabrication and electrical characterization of vacuum deposited n-CdTe/p-ZnTe heterojunction diodes 真空沉积n-CdTe/p-ZnTe异质结二极管的制备和电学特性
K. V. Bangera, K. Gowrish Rao, G. Shivakumar
The study of n-CdTe/p-ZnTe heterojunctions is of vital importance for the fabrication of single junction and tandem solar cells. In the present research work n-CdTe/p-ZnTe heterojunction diodes were prepared by high vacuum deposition technique. The growth conditions required for obtaining desired quality n-CdTe and p-ZnTe films were optimized by performing a series of trials. The n-CdTe/p-ZnTe heterojunctions were prepared by fist depositing CdTe film on glass substrate and then depositing ZnTe flim on top of CdTe. Detailed electrical characterization of the heterojunction was performed. The conduction in the heterojunction was predominantly due to thermionic emission at low voltages. However at higher voltages space charge limited conduction was found to be dominant. Many technically important parameters such as barrier height, width of the depletion region, carrier concentration etc were deduced by studying the I–V and C-V characteristics of the heterojunction. The activation energies of ZnTe and CdTe were determined by studying the variation of resistance with ambient temperature and a theoretical band diagram of the heterojunction was drawn using Anderson's model.
n-CdTe/p-ZnTe异质结的研究对于单结和串联太阳能电池的制造具有重要意义。本研究采用高真空沉积技术制备了n-CdTe/p-ZnTe异质结二极管。通过一系列试验,优化了制备高质量n-CdTe和p-ZnTe薄膜所需的生长条件。首先在玻璃衬底上沉积CdTe薄膜,然后在CdTe表面沉积ZnTe薄膜,制备了n-CdTe/p-ZnTe异质结。对异质结进行了详细的电学表征。异质结中的传导主要是由于低电压下的热离子发射。然而,在较高的电压下,空间电荷限制传导占主导地位。通过研究异质结的I-V和C-V特性,推导出了势垒高度、耗尽区宽度、载流子浓度等重要技术参数。通过研究ZnTe和CdTe的电阻随环境温度的变化来确定其活化能,并利用Anderson模型绘制了异质结的理论能带图。
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引用次数: 2
Covalent immobilization of tyrosinase onto commercial multi-walled carbon nanotubes and its effect on enzymatic activity 商用多壁碳纳米管上酪氨酸酶的共价固定化及其对酶活性的影响
Pub Date : 2010-12-01 DOI: 10.1109/ESCINANO.2010.5701046
Tai Boon Kai, Z. Abdul Majid, S. Shahir
Multi-walled carbon nanotubes (MWCNTs) exhibit unique structural, electrical, mechanical, electrochemical, and chemical properties [1]. Moreover, the possibility of modifying their surface properties through different methods has stimulated increasing interest in their application as components in biosensors. In this sense, it is possible to employ carbon nanotubes as support to immobilize enzymes.
多壁碳纳米管(MWCNTs)具有独特的结构、电学、力学、电化学和化学性质[1]。此外,通过不同方法修饰其表面特性的可能性刺激了它们作为生物传感器组件应用的兴趣。从这个意义上说,利用碳纳米管作为固定化酶的载体是可能的。
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引用次数: 1
A linear 0.18um CMOS Distributed Low Noise Amplifier from 3.1 to 10.6 GHz with cascode cells 一种线性0.18um CMOS分布低噪声放大器,频率为3.1至10.6 GHz,带级联单元
S. Shamsadini, F. Kashani, Neda Bathaei
In this paper, we propose a design methodology of 3.1–10.6GHz Ultra-wideband (UWB) Distributed Low Noise Amplifier using standard TSMC 0.18um CMOS technology. The four cells DLNA, each cell contains cascode architecture, can be use in broadband applications. The proposed distributed low noise amplifier has an appropriate input and output matching over the full band of 3.1–10.6 GHz. We achieve acceptable results for low noise amplifier as a flat power gain of 12dB (S21) from 3.1 to 10.6GHz, which is ripple only ±0.3 dB over the full UWB band. The proposed DLNA has an excellent linear behavior. The third intercept point (IIP3) of the proposed DLNA is +2dBm and P1dBin is −12dBm. An input impedance matching is <−15 dB (S11) and an output impedance matching of < −15 dB (S22) over the entire band. This LNA achieves the minimum noise figure of 2.8dB.
在本文中,我们提出了一种3.1-10.6GHz超宽带(UWB)分布式低噪声放大器的设计方法,该放大器采用标准台积电0.18um CMOS技术。四个单元DLNA,每个单元包含级联编码架构,可用于宽带应用。所提出的分布式低噪声放大器在3.1-10.6 GHz全频段内具有合适的输入输出匹配。我们在3.1至10.6GHz范围内获得了12dB (S21)的平坦功率增益,在整个UWB频段内纹波仅为±0.3 dB,从而获得了可接受的低噪声放大器结果。所提出的DLNA具有良好的线性特性。该DLNA的第三个截距点(IIP3)为+2dBm, P1dBin为- 12dBm。输入阻抗匹配为<−15 dB (S11),输出阻抗匹配为<−15db (S22)在整个频带。该LNA的最小噪声系数为2.8dB。
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引用次数: 1
Changes in physical properties and molecular structure of polystyrene nanospheres exposed with daily solar flux 日晒下聚苯乙烯纳米球物理性质和分子结构的变化
P. J. Wibawa, M. Agam, Hadi Nur, H. Saim
The effects of physical properties and molecular structure of 200 nm polystyrene nanospheres (PSN) coated on silicon wafer exposed with daily solar flux were explored by field emission scanning electron microscope (FE-SEM) and attenuated total reflectance-Fourier transform infrared (ATR-FT-IR) spectrometer. It is revealed that the particles shape of PSN changed from spheric to eight-shaped after solar radiation. Reduction of the size as much as 29.5% after 5 minutes exposure was also observed in PSN particles. Changes in the molecular structure of the PSN particles after solar radiation were observed where some of the phenyl moieties of polystyrene broke down to facilitate carbon-carbon cross linkage bonds. These results demonstrated that the shrinkage of PSN particles is caused by the change of the molecular structure of polystyrene.
利用场发射扫描电镜(FE-SEM)和衰减全反射-傅里叶变换红外光谱仪(ATR-FT-IR)研究了日晒下硅片表面涂覆200 nm聚苯乙烯纳米微球(PSN)的物理性质和分子结构的影响。结果表明,在太阳辐射作用下,PSN的粒子形状由球状变为八字形。PSN颗粒在暴露5分钟后也缩小了29.5%。在太阳辐射后,PSN粒子的分子结构发生了变化,聚苯乙烯的一些苯基部分被分解以促进碳-碳交叉键的形成。这些结果表明PSN颗粒的收缩是由聚苯乙烯分子结构的变化引起的。
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引用次数: 7
Heating effect of a one-dimensional molecular assembly on self-repairing capability in the nanoscopic channels of mesoporous silica 一维分子组装对介孔二氧化硅纳米通道中自修复能力的加热效应
Pub Date : 2010-12-01 DOI: 10.1109/ESCINANO.2010.5700970
Hendrik Oktendy Lintang, K. Kinbara, T. Yamashita, T. Aida
Self-repairable optoelectronic devices from a heat-induced structural damaged are potentially important for sensor [1] and display [2] applications. Recently, self-healing phenomena have attracted particular attention for developing sustainable structural materials [3], where extensive studies have been reported on polymeric materials capable of autonomous repairing macroscopic fractures or restoration lost mechanical strengths [4, 5]. On the other hand, for exploiting molecular devices that can self-repair elaborate functions, one may encounter different problems originating from much smaller size regimes. However, no rational strategies have yet been proposed for addressing this challenging issue. In our previous paper, when a phosphorescent columnar assembly of trinuclear gold(I) pyrazolate complex [Au3Pz3] is confined in the nanoscopic channel of hexagonal mesoporous silica [Au3Pz3]/silicahex (Fig. 1), upon stepwise heating from 20 °C to 140 °C in 45 min, the one-dimensional molecular assemblies are not only protected from thermal disruption but also strongly encouraged to self-recover to 100% in 5 h from a heat-induced structural damaged [6].
热致结构损伤的自修复光电器件对于传感器[1]和显示器[2]的应用具有潜在的重要意义。最近,自修复现象在可持续结构材料的开发中引起了特别的关注[3],其中大量研究报道了能够自主修复宏观骨折或恢复失去的机械强度的聚合物材料[4,5]。另一方面,为了开发能够自我修复复杂功能的分子装置,人们可能会遇到来自更小尺寸体系的不同问题。然而,目前还没有提出合理的策略来解决这一具有挑战性的问题。在我们之前的论文中,当三核金(I)吡唑酸配合物[Au3Pz3]的磷光柱状组装体被限制在六方中孔二氧化硅[Au3Pz3]/硅己烯的纳米通道中(图1),在45分钟内从20°C逐步加热到140°C时,一维分子组装体不仅不受热破坏,而且强烈鼓励在5小时内从热引起的结构损伤中自我恢复到100%[6]。
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引用次数: 6
Effect of chirality on the silicon-carbon nanotube thermal interface resistance 手性对硅碳纳米管热界面电阻的影响
Pub Date : 2010-12-01 DOI: 10.1109/ESCINANO.2010.5700955
M. Osman, Taejin Kim
Thermal flow across the interface between two different materials is strongly affected by the differences in the electronic properties and vibrational modes of the two materials which give rise to the thermal interface resistance[1]. The thermal interface resistance results in a finite temperature discontinuity at the interface between the two materials. Reducing the thermal interface resistance between silicon chips and the packaging material is very critical for efficiently extracting heat and ensuring reliable operation of ICs. The large thermal conductivity of carbon nanotubes makes them very ideal for developing thermal switches and thermal interface materials [2]. We have investigated the thermal interface resistance between carbon nanotubes and silicon using molecular dynamic (MD) simulations.
通过两种不同材料界面的热流受到两种材料的电子特性和振动模式差异的强烈影响,从而产生热界面阻力[1]。热界面电阻导致两种材料界面处的有限温度不连续。降低硅芯片与封装材料之间的热界面电阻对于有效地提取热量和确保集成电路的可靠运行至关重要。碳纳米管的高导热性使其成为开发热开关和热界面材料的理想材料[2]。本文采用分子动力学方法研究了碳纳米管与硅之间的热界面电阻。
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引用次数: 0
Nanotechnology for solid-state lighting 用于固态照明的纳米技术
Pub Date : 2010-12-01 DOI: 10.1109/ESCINANO.2010.5701097
Chua Soo Jin
Lighting has evolved over the last 150 years from the primordial use of fire, incandescence from filaments, to fluorescence and electrical discharge in gases. The use of each new material has led to the improvement in luminous efficacy by an order of magnitude. The incandescent light bulb, invented by Edison in 1879, will be phased out over the next few years as governments sought to ban its manufacture and use because of its low efficiency (< 5%) and to introduce green technology. The fluorescent lamp, which is widely used to replace the incandescent bulb with its use of mercury and presence of lead in some phosphors, is seen as an interim measure.
在过去的150年里,照明已经从最初的火、灯丝的白炽灯发展到荧光和气体放电。每一种新材料的使用都使发光效率提高了一个数量级。1879年爱迪生发明的白炽灯泡将在未来几年内逐步淘汰,因为各国政府试图禁止白炽灯泡的生产和使用,因为它的效率很低。(5%)及引进绿色科技。荧光灯被广泛用于取代白炽灯,因为它使用汞,一些荧光粉中含有铅,被视为一种临时措施。
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引用次数: 0
Growth of Au-catalyzed and self-catalyzed ZnO nanowires using chemical vapor deposition technique 化学气相沉积法生长au催化和自催化氧化锌纳米线
Pub Date : 2010-12-01 DOI: 10.1109/ESCINANO.2010.5700937
Pu Yong, Choy Kwang Leong, Hou Xianghui
With the ongoing miniaturization of devices such as FETs [1], the synthesis of ZnO NWs (building blocks) has attracted extensive research interest. ZnO NWs have been synthesized via different routes by many research groups [2–4]. In order for these building blocks to be incorporated into functional nano-devices, controlled synthesis of the ZnO NWs to obtain features such as the desired size, shape and alignment should be fulfilled. This is a rather challenging task. A better understanding of the growth mechanism of ZnO NWs may be helpful to resolve these uncertainties. However, the underlying mechanism for the growth of the ZnO NWs for both self-catalyzed and Au-catalyzed ZnO NWs, have not been well elucidated. In addition, there is no fully developed cohesive model that explains the growth mechanism of both self-catalyzed and Au-catalyzed ZnO NWs.
随着fet[1]等器件的不断小型化,ZnO NWs(构建块)的合成引起了广泛的研究兴趣。许多研究小组已经通过不同的途径合成了ZnO纳米波[2-4]。为了将这些构建块整合到功能纳米器件中,必须控制ZnO NWs的合成以获得所需的尺寸,形状和排列等特征。这是一项颇具挑战性的任务。更好地了解ZnO NWs的生长机制可能有助于解决这些不确定性。然而,自催化和au催化ZnO NWs生长的潜在机制尚未得到很好的阐明。此外,目前还没有完整的内聚模型来解释自催化和au催化的ZnO NWs的生长机制。
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引用次数: 1
期刊
2010 International Conference on Enabling Science and Nanotechnology (ESciNano)
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