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Digest of Papers. Microprocesses and Nanotechnology'98. 198 International Microprocesses and Nanotechnology Conference (Cat. No.98EX135)最新文献

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Bulk Modification In An Optical Fiber Using a High-Intensity Femtosecond Laser 利用高强度飞秒激光对光纤进行体改性
Sung-Hak Cho, H. Kumagai, K. Midorikawa, M. Obara
The solid-density plasma formation and induced modification have recently been a major concern since the advent of a high-intensity femtosecond laser.' The solid-density plasma formation is attributed to contributions from both self-focusing from the intensity-dependent refractive index and self-defocusing resulting from ionization.2 Recently, laser-induced bulk modification in transparent materials has been found to yield new tools for ultra-precise three-dimensional micromachining of small, complex-shaped components of transparent dielectrics and polymers for optoelectronic, micro optic, and fiber technological application^.^ This has also provided useful microstructuring technology for application of waveguide and memory in transparent material because refractive index change of induced modification is increasing. Although experiments for bulk modification in solids using high-powr femtosecond laser pulses have been reported: the process of laser-induced modification in a transparent material for number of input pulses have not been clarified yet in detail. In this paper, for the first time to our knowledge, the experimental observation of laser induced bulk modification process in a multimode optical fiber excited by a high intensity (above lo'* W/cm') femtosecond Ti:sapphire laser. In our experiment, a multimode optical fiber was used, which enabled one to easily in situ study the process of laser-induced modification for various number of laser pulses. The schematic diagram of the experimental setup for laser-induced modification in an optical fiber is shown in Fig. 1. A multimode optical fiber (step index) with 200/220 pm corekladding diameters (Newport F-MCC-T) was used. The core of the optical fiber is composed of pure silica. Moreover, the optical fiber is a high-temperature one in order to increase the fiber damage threshold when powerful laser pumping is employed. Ti:sapphire oscillator amplifier laser system (h,=790 nm) with 110 fs pulse duration, 1 W average output power, and 1 kHz repetition rate was used as a pumping source. The number of laser pulse was controlled by electric shutter. The 5-mm-diameter beam was focused through a focusing lens ( f = 60 mm ) and injected into the optical fiber which was located further away than the breakdown point. The average input intensity of the laser beam at the optical fiber location was controlled using neutral-density filters that were inserted between the laser and the focal lens. The length of optical fiber was 10 cm. When the input intensity exceeded 1 . 5 ~ 1 0 ' ~ W/cm2, self-channeled plasma formation was observed with a length of 8 10 mm from the input end of optical fiber. The side views of the plasma formation were observed in situ using a microscope and recorded using a CCD camera. (Fig. 2) When self-channeled plasma formation occurred at the input intensity of 1 . 5 ~ 1 012W/cm', the process of laser-induced modification was obsevered using a microscope by controlling the number
自从高强度飞秒激光器问世以来,固体密度等离子体的形成和诱导修饰一直是人们关注的主要问题。”固体密度等离子体的形成归因于强度相关折射率的自聚焦和电离引起的自散焦最近,在透明材料中激光诱导的体改性已经被发现为用于光电子、微光学和光纤技术应用的透明电介质和聚合物的小型、复杂形状部件的超精密三维微加工提供了新的工具^。^这也为透明材料中波导和存储器的应用提供了有用的微结构技术,因为诱导修饰的折射率变化越来越大。虽然使用高功率飞秒激光脉冲在固体中进行体改性的实验已有报道,但在透明材料中对输入脉冲数进行激光诱导改性的过程尚未得到详细的阐明。本文首次在我们所知的范围内,实验观察了高强度(大于lo'* W/cm')飞秒Ti:蓝宝石激光激发的多模光纤中激光诱导体修饰过程。在我们的实验中,我们使用了一种多模光纤,这使得我们可以很容易地在现场研究不同数量的激光脉冲的激光诱导修饰过程。光纤激光诱导修饰实验装置示意图如图1所示。采用200/220 pm包芯直径的多模光纤(阶跃指数)(Newport f - mct)。光纤的芯是由纯二氧化硅构成的。此外,为了提高强激光抽运时光纤的损伤阈值,光纤是高温光纤。采用脉冲持续时间为110 fs、平均输出功率为1 W、重复频率为1 kHz的Ti:蓝宝石振荡放大器激光系统(h,=790 nm)作为泵浦源。激光脉冲数由电动快门控制。直径为5mm的光束通过聚焦透镜(f = 60 mm)聚焦,注入到距离击穿点更远的光纤中。通过在激光器和焦透镜之间插入中性密度滤光片来控制光纤位置处激光束的平均输入强度。光纤长度为10cm。当输入强度超过1。在5 ~ 10′~ W/cm2处,观察到距离光纤输入端长度为8 ~ 10 mm的自通道等离子体形成。用显微镜原位观察等离子体形成的侧视图,并用CCD相机记录。(图2)当输入强度为1时,自通道等离子体形成。5 ~ 1 012W/cm’,通过控制激光脉冲数,在显微镜下观察激光诱导修饰的过程。修改区域的显微侧视图如图3所示。在包覆直径为200/220 pm的光纤中,经过5分钟后,观察到体积改性的直径约为5pm,长度约为6mm(3)。不同输入强度下的激光诱导修饰。由于自聚焦效应,第一个修饰点位于距离光纤输入端72pm的位置,其直径约为5pm。3 × 105次照射后,不同输入强度下激光诱导修饰的直径变化如图4所示。改性直径47pm由激光输入强度控制。综上所述,对具有双包层光纤结构的光多模光纤进行改性,在光纤激光器和光纤放大器的各种应用中是一种有用的方法。利用自通道等离子体形成的飞秒激光诱导修饰技术为透明材料的超精密三维修饰和微加工提供了复杂的工具,而不会破坏残余材料。
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引用次数: 0
High-Speed Convolution System For Real-Time Proximity Effect Correction 实时接近效应校正的高速卷积系统
S. Oogi, T. Ishimura, T. Kamikubo, M. Shimizu, Y. Hattori, T. Iijima, H. Anze, T. Abe, T. Tojo, T. Takigawa
In order to realize a real-time proximity effect correction system, a high-speed, highly accurate hardware system for convolution calculation has been developed. The representative figure method is used in the system. Pipeline architecture and parallel processing architecture are also used. The calculation speed of the system is 500 s for a writing region of 10 ×10 cm. The optimum correction dose has been evaluated using the output data of the convolution system. The error in the correction dose caused by our system is found to be 0.5% at most. These results suggest that a real-time proximity effect correction system can be realized, which can be used for making reticles of Gbit-class dynamic ramdom access memories (DRAMs).
为了实现实时接近效应校正系统,研制了一种高速、高精度的卷积计算硬件系统。系统采用了代表性图形法。还采用了流水线架构和并行处理架构。对于10 ×10 cm的写入区域,系统的计算速度为500s。利用卷积系统的输出数据对最佳校正剂量进行了评估。我们的系统造成的校正剂量误差不超过0.5%。这些结果表明,可以实现实时接近效应校正系统,该系统可用于制作gb级动态随机存取存储器(dram)的网格。
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引用次数: 2
Nanofabrication Using Scanning Near-Field Optical Microscopy 使用扫描近场光学显微镜的纳米制造
Y. Mitsuoka, K. Nakajima, N. Chiba, H. Muramatsu, T. Ataka
The interest in extremely small solid-state devices and high-density data storage has increased rapidly. To realize such applications, new techniques for fabricating nanometer-scale structures are important, because the conventional optical lithography has an insufficient resolution limited by the wavelength of the light and the numerical aperture of the lenses. In addition to electron beam lithography, scanning probe techniques such as scanning tunneling microscopy (STM)’) and atomic force microscopy (AFM)’) have been investigated to perform surface modifications in a simple way. Near-field optical lithography has a potential to fabricate nanometer-scale patterns more rapidly than the techniques based on STM or AFM. Scanning near-field optical microscopy (SNOM) is a useful method to investigate the possibility of near-field optical lithography for nanometer-scale fabrication. The schematic diagram of our SNOM3) system for the fabrication is shown in Fig. 1. An optical fiber probe has an aperture with a subwavelength at the apex. The optical fiber probe is bent and vibrated vertically to control the distance between the sample and the probe tip. The light source is an Ar ion laser (A = 488 nm) or a He-Cd laser (A = 442 nm). Commercial photoresist, which is sensitive to g line (A = 436 nm), is coated on a Si wafer by a spin-coater. The photoresist film is exposed by the light emitted by the aperture of the optical fiber probe. Changing the incident light intensity or the scanning speed controls the exposure conditions. The exposed photoresist film is developed and observed by AFM. Figure 2 shows the AFM image of the positive photoresist film. The groove width in the photoresit film is about 100 nm. It is nearly equal to the aperture size of the optical fiber probe. In Fig. 3, an aluminum line pattern with the width of 100 nm on a Si wafer was fabricated by the lift-off technique. We have demonstrated that subwavelength patterns can be fabricated using SNOM. These results show the possibility of near-field optical lithography for fabricating nanometer-scale structures.
对极小的固态设备和高密度数据存储的兴趣迅速增加。由于传统的光学光刻技术受光的波长和透镜的数值孔径的限制,分辨率不足,因此要实现这种应用,制造纳米级结构的新技术是很重要的。除了电子束光刻,扫描探针技术,如扫描隧道显微镜(STM)和原子力显微镜(AFM)已经被研究,以一种简单的方式进行表面修饰。与基于STM或AFM的技术相比,近场光学光刻技术具有更快地制造纳米尺度图案的潜力。扫描近场光学显微镜(SNOM)是研究近场光刻技术用于纳米制造的一种有效方法。我们用于制造的snom系统的示意图如图1所示。一种光纤探头在其尖端有一个亚波长的孔径。光纤探头垂直弯曲和振动,以控制样品和探头尖端之间的距离。光源为Ar离子激光器(A = 488 nm)或He-Cd激光器(A = 442 nm)。商用光刻胶对g线(A = 436 nm)敏感,通过旋转涂层机涂覆在硅晶片上。光刻胶薄膜由光纤探头孔径发出的光暴露。改变入射光强度或扫描速度可以控制曝光条件。利用原子力显微镜对曝光的光刻胶薄膜进行显影和观察。图2显示了正光刻胶薄膜的AFM图像。光阻膜的沟槽宽度约为100nm。它几乎等于光纤探头的孔径大小。在图3中,我们利用发射技术在硅晶片上制备了宽度为100 nm的铝线图案。我们已经证明了亚波长模式可以用SNOM制造。这些结果显示了近场光学光刻技术用于制造纳米级结构的可能性。
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引用次数: 0
Totally Different Sputter Damage Profiles Of Metal And Si Single Crystal Smrfaccs Investigated By Medium Energy Ion Scattering Spectroscopy 用中能离子散射光谱研究金属和硅单晶表面完全不同的溅射损伤特征
D. Moon, Y. Ha, Hyun Kong Kim, Sehoon Kim
IJnderstanding the radiation damage cluc to low energy ion boiiibxdnient has IXY~I i o i i c ' ( 1 1 Generally. it has been i-egardcd lor :I lorig I imc . the major issues in sputtering and etching that the energetic keV ion bombardment dcsti-oys the su~face crystalline tixtcture 111) 1 ( I anioiyhization. However, most of the radiation damage studies have been basecl on I A J Energy Electron Dilfraction (LEED). €Iowever. the LEED results are not sensitive. to ih( non-periodic local atomic structure, because the coherent lengths of the electrons lx i i ' i i l l(4 ( ( I the surface are -1 to 10nni. It has been shown that niedlum energq ion scalterinK spectroscopy (i?lEIS 1 is a powerid tool foiinvesligating atomic stiiictiu-e and comwisi l ion profiles with a couple of atomic layer depth resolution. Since the channeling and blocl~ii rg effects are mainly detei-nined by the neighboring atoms, the stiiicti1ral infomiations (~ l ) t~ i i i ivd from MEIS are local in the nature in contrast to the periodic long range ordered st i -uc~l i i i~c €rom LEED. the radiation damage formed by low enei-gk ion beam sput tei-ing. Therefore, MEIS has unique features to probe local s~-~ichual changc tlut. to
对低能离子辐射损伤的认识一般有IXY~I ~I ~I ~I ~I ~I ~I ~I ~I ~I ~I ~I ~I ~I ~I ~I ~I ~I ~I ~I ~I ~(1)。它一直是我最喜欢的东西。在溅射和蚀刻中,高能离子轰击会破坏表面晶状织构的主要问题。然而,大多数的辐射损伤研究都是基于能量电子衍射(LEED)。€Iowever。LEED的结果不敏感。到ih(非周期性局部原子结构),因为电子的相干长度lx i i i i i l l(4) i表面为-1至10nni。研究表明,铌能量离子散射ink光谱(i?lEIS - 1是一个强大的工具,用于研究原子的科学和化学离子剖面,具有几个原子层深度分辨率。自引导和blocl ~二世rg效果主要由邻近的原子,detei-nined的stiiicti1ral infomiations (~ l) t ~我我我从MEIS试管是当地的自然与周期性的远程命令圣我加州大学~ l我我~ c€罗LEED。低能量gk离子束溅射形成的辐射损伤。因此,MEIS具有独特的特征来探测局部的s~- - -文化变化。来
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引用次数: 0
Determination Of The CD Dispersion And Proximity Bias Across The Lens Field By Electrical Linewidth Measurements 用电线宽测量法测定CD在透镜场中的色散和接近偏置
O. Toublan, D. Boutin, P. Schiavone
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引用次数: 1
MoSi(N) As A Diffusion Barrier Between Cu And Si MoSi(N)作为Cu和Si之间的扩散势垒
J. Park, Y.H. Lee, J. Bae, G. Yeom, J. Song
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引用次数: 0
OPC Methodology To Overcome Mask Error Effect On Below 0.25 um Lithography Generation 在0.25微米以下光刻中克服掩模误差影响的OPC方法
Keeho Kim, S. Madhavan, J. Lilygren
1. Motivation Lithography for below 0.25 um generation strongly demands OPC(Optica1 Proximity Correction) technics to achieve the better pattem fidelity that normally improves overlay margin, CD tolerance, Device characteristics such as leakage current margin and etc. The first step to design mask layout having OPC should be simulation. Normally, the main tasks of this simulation step are of making decision the best type and dimension of OPC. However, sometimes real pattern results on wafer level exposed by the mask that is designed with based on simulation, are different from designer’s expectation. This phenomenon is explicitly getting worse and worse due to the increasing of mask error when going to 4 x reticle and aggressive OPC patterns for below 0.25 um generation device. In this paper, we try to build up new simulation methodology to obtain the better matching results between simulation and real experimental results.
1. 0.25 um以下一代的激励光刻强烈要求OPC(光学邻近校正)技术,以实现更好的模式保真度,通常可以改善覆盖裕度,CD公差,漏电流裕度等器件特性。设计具有OPC的掩模布局的第一步应该是仿真。通常,该仿真步骤的主要任务是确定OPC的最佳类型和尺寸。然而,基于仿真设计的掩模所暴露的晶圆级上的真实图案结果有时与设计者的期望不同。对于低于0.25 um的生成设备,当达到4倍网线和侵略性OPC模式时,由于掩模误差的增加,这种现象显然变得越来越糟。本文试图建立一种新的仿真方法,使仿真结果与实际实验结果更好地匹配。
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引用次数: 0
Fabrication Of Bimetallic Cantilevers For Chemical Sensors 化学传感器用双金属悬臂梁的制备
M. Jung, D. Kim, S.S. Choi, O.J. Kang, Y. Suh, Y. Kuk
There have been great interests in developing micromachined cantilever stylus, scanning probe based chemical sensor, including thermal probe Sensor and nano-resolution mass and molecule detectors. The microfabricated cantilevers offer various possibilities as chemical sensors such as nanocalorimeters on high resolution mass detectors based on resonance frequency shift. The microcantilever coated with a thin metal layer was recently reported as a high sensitive thermal Sensor when heat was generated by reaction of hydrogen and oxygen on the cantilever in vacuum. Nanoscale mass measurement was reported in particulate mass deposited on microcantilevers using resonance frequency shifl techniques. Bing et al. also proposed a micro cantilever sensor with MHz resonance frequency and a mass resolution of IO-'* g. More recently, vapor adsorption on the micro cantilever surface was also found to create a shift of resonance frequency and angular bending of the bimetallic cantilevefll,2,3,4,5]. In this work, we fabricated a Si3N4 cantilever using micromachining techniques. Initially a Si,N, layer was deposited using low pressure chemical vapor deposition techniques. The cantilever was defined and patterned by photolithography on the front side and etched into the silicon. Finally, the backside etching was performed until both etch fronts meet and the cantilever becomes released. -100nm AJ and 20nm Pt thin film layers were deposited on the backside of the fabricated S13N, cantilever using electron beam evaporator. The temperature change and heat flow across the fabricated bimetallic lever would create angular bending of the bimetallic cantilever. The heat was supplied through a stainless steel block attached to a cantilever-supporting beam. The block was wrapped with a nichrome wire in order to supply heat to the lever. The thenal couple was also attached to the stainless steel block. The hysteris curve of the lever upon heating and cooling was measured without a chemical substance. The chemical substance, tetra decand CH3(CH2),,0H, was used and its theoretical temperature for phase change from solid phase to liquid phase is known to be -31 3K. Very tiny amounts of tetra decanol were placed on top of the bimetallic lever and its thermal response was examined during an endothermic chemical reaction using optical deflection method. The abrupt change of the angular bending of the bimetallic lever due to endothermic chemical reactions was observed at -315K. This introductory experiment presents bimetallic cantilevers as excellent candidates for chemical Sensor (sensitive in mass resolution) in an atmospheric environment. Depending upon chemical reaction, whether it is exothermic or endothermic, specific micro-scale or nano-scale cantilever sensors can be tailored to the specific chemical reaction of the interest.
微机械悬臂笔、基于扫描探针的化学传感器(包括热探针传感器)和纳米分辨率质量和分子探测器的开发引起了人们的极大兴趣。基于共振频移的高分辨率质量探测器上的纳米量热计等化学传感器提供了多种可能性。在真空条件下,氢和氧在微悬臂梁上发生反应产生热量,并包覆金属薄层的微悬臂梁是一种高灵敏度的热传感器。采用共振换频技术对微悬臂梁上沉积的颗粒进行了纳米尺度的质量测量。Bing等人还提出了一种谐振频率为MHz、质量分辨率为IO-'* g的微悬臂传感器。最近,研究人员还发现,微悬臂表面的蒸气吸附会导致共振频率的偏移和双金属悬臂的角弯曲[2,3,4,5]。在这项工作中,我们使用微加工技术制作了Si3N4悬臂梁。最初采用低压化学气相沉积技术沉积Si,N层。悬臂被定义和图案的光刻在正面和蚀刻到硅。最后,进行背面蚀刻,直到两个蚀刻面相遇,悬臂被释放。利用电子束蒸发器在制备的S13N的背面悬臂沉积-100nm的AJ和20nm的Pt薄膜层。温度变化和热流穿过所制造的双金属杠杆将产生双金属悬臂的角度弯曲。热量通过附着在悬臂支撑梁上的不锈钢块提供。为了给杠杆提供热量,块被镍铬合金丝包裹着。金属对也连接在不锈钢块上。在不添加化学物质的情况下,测量了杠杆在加热和冷却时的滞后曲线。化学物质为四癸烷CH3(CH2),,0H,已知其固相到液相相变的理论温度为-31 3K。将极少量的四癸醇置于双金属杠杆的顶部,并在吸热化学反应中使用光学偏转法检测其热响应。在-315K时,观察到双金属杠杆的角度弯曲因吸热化学反应而发生突变。本实验介绍了双金属悬臂梁作为大气环境中化学传感器(敏感的质量分辨率)的优秀候选者。根据化学反应,无论是放热还是吸热,特定的微尺度或纳米尺度悬臂式传感器都可以针对特定的化学反应进行定制。
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引用次数: 0
Self-Assembled Quantum Dot Single Electron Devices 自组装量子点单电子器件
S.K. Jung, B. Choi, S.I. Kim, C.K. Hyun, B. Min, S. Hwang, J. Park, Y. Kim, E. Kim, S. Min
Single electron tunneling and its application to future VLSI systems has been an important subject extensively studied for the last decade [l]. Many types of materials and ideas have been applied to fabricate and implement single electron devices operating at high temperatures. The self-assembled quantum dot (SAQD) system is one of the attractive candidates for single electron devices since high quality Coulomb islands can be obtained in one-step growth processes. Furthermore, the characteristic energy scale of the devices would enhance because the quantum energy is expected to be added to the classical charging energy. on InGaAs SAQD's. lever-arms with nm spacings. staircases at 77 K and higher temperatures. Figure 1 (a) and (b) show an AFM photos of typical SAQD single electron devices fabricated by the lever-arm technique. The InGaAs SAQD's we have used were grown by an MOCVD technique and the typical diameter of the dots is approximately 20 nm [2]. The aluminum lever-arms with spacings from 200 to 40 nm were fabricated by a standard ebeam exposure and a lift-off process. Figure 2 (a) and (b) show the 77 K current-voltage (I V) and its differential conductance - voltage characteristics.(dUdV - V) of lever - arm device with the gap of 40 nm. Several staircases are clearly identified in both the I-V and the dVdV-V. dI/dV-V of the device with the gap of 150 nm. Clear staircases are also seen. These staircases are originated from the single electron tunneling through SAQD's located in the shortest current path between two lever - arms. In conclusion, self-assembled guantum dot single electron devices are made by the lever-arm technique with the minimum gap spacing of 40 nm and clear staircases are observed in the I-V characteristics. The result of more complicated devices with multiple lever-arms will also be presented at the conference.
近十年来,单电子隧穿及其在未来VLSI系统中的应用一直是一个被广泛研究的重要课题[1]。许多类型的材料和思想已经被应用于制造和实现在高温下工作的单电子器件。自组装量子点(SAQD)系统由于可以在一步生长过程中获得高质量的库仑岛而成为单电子器件的有吸引力的候选者之一。此外,由于量子能量有望被添加到经典充电能量中,因此器件的特征能量尺度将得到增强。在InGaAs SAQD上。间距为nm的杠杆臂。在77度或更高温度下的楼梯。图1 (a)和(b)显示了利用杠杆臂技术制造的典型SAQD单电子器件的AFM照片。我们使用的InGaAs SAQD是通过MOCVD技术生长的,其典型直径约为20 nm[2]。铝杆臂的间距从200到40纳米是由标准的电子束曝光和提离工艺。图2 (a)和(b)显示了77k电流-电压(I V)及其差分电导-电压特性。(dUdV - V),间隙为40nm。在I-V和dVdV-V中都可以清楚地识别出几个楼梯。器件的dI/dV-V差为150nm。清晰的楼梯也可以看到。这些阶梯是由位于两个杠杆臂之间的最短电流路径上的SAQD的单电子隧穿引起的。综上所述,利用杠杆臂技术制备了自组装的量子点单电子器件,最小间隙为40 nm,在I-V特性上观察到明显的阶梯状结构。带有多个杠杆臂的更复杂设备的结果也将在会议上展示。
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引用次数: 0
Progress In The Development Of Extreme Ultraviolet Lithography Exposure Systems 极紫外光刻曝光系统的研究进展
A. Ray-Chaudhuri
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引用次数: 1
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Digest of Papers. Microprocesses and Nanotechnology'98. 198 International Microprocesses and Nanotechnology Conference (Cat. No.98EX135)
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