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2021 IEEE 16th Nanotechnology Materials and Devices Conference (NMDC)最新文献

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Giant Polarization in Nanodielectrics: (Invited Paper) 纳米电介质中的巨极化:(特邀论文)
Pub Date : 2021-12-12 DOI: 10.1109/NMDC50713.2021.9677542
C. Homes
The relative permittivity of a material is a scaling factor for capacitors and the devices based upon them; the larger the relative permittivity, the greater the degree of miniaturization, or potential for energy storage. Materials with a relative permittivity than that of silicon nitride (approximately 7) are referred to as high-dielectric constant materials. Values of about 100 are typical in titanium dioxide rutile. Values of about 10,000 are observed in barium titanate in the region of the ferroelectric transition, which while impressive, is not very useful due to the strong temperature dependence. The observation of a relative permittivity of over 100,000 in the calcium copper titanate material sparked considerable interest because it showed little temperature dependence between 100 and 600 K over most of the radio-frequency range. Further investigation revealed that this material appears to be naturally nanotextured and that the colossal permittivity was likely due to the surface and/or internal barrier layer capacitance effect, although the issue is not settled. Unfortunately, the dielectric losses in this class materials are relatively high. A new strategy to achieve high dielectric permittivity with low loss involves using localized lattice defect states through ambipolar co-doping; these intrinsic defect complexes give rise to strong dipoles that are responsible for a relative permittivity of 10,000 with exceptionally low dielectric losses over most of the radio frequency range and excellent thermal stability.
材料的相对介电常数是电容器和基于它们的器件的比例因子;相对介电常数越大,微型化程度或储能潜力就越大。相对介电常数大于氮化硅(约为7)的材料称为高介电常数材料。二氧化钛金红石的典型值约为100。在钛酸钡的铁电跃迁区域中观察到约10,000的值,虽然令人印象深刻,但由于强烈的温度依赖性,这不是很有用。观察到钛酸铜钙材料的相对介电常数超过100,000,引起了相当大的兴趣,因为在大多数射频范围内,它在100到600 K之间的温度依赖性很小。进一步的研究表明,这种材料似乎是天然的纳米纹理,而巨大的介电常数可能是由于表面和/或内部阻挡层电容效应,尽管这个问题尚未解决。不幸的是,这类材料的介电损耗相对较高。利用局域晶格缺陷态通过双极性共掺杂实现高介电常数和低损耗的新策略;这些内在缺陷复合物产生了强偶极子,其相对介电常数为10,000,在大多数射频范围内具有极低的介电损耗和优异的热稳定性。
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引用次数: 0
Energy-efficient Flexible Ammonia Sensors Enabled by Polypyrrole-Graphene 聚吡咯-石墨烯实现的节能柔性氨传感器
Pub Date : 2021-12-12 DOI: 10.1109/NMDC50713.2021.9677543
Xiao Xu, Zhehan Wang, Ke Zhan, Chenxu Bao, Zhengru Zhu, Bo Chang, Qichao Chen, Xu Jing, Li Tao
Two Dimensional (2D) materials and their combination with conductive polymers are emerging candidates for high-performance gas sensing with desirable mechanical flexibility. It is of great importance to understand the influence of applied strain to the sensing performance of such flexible sensors. In this work, we investigated the combination of graphene and polypyrrole (PPy) as flexible sensor devices and explored their ammonia sensing performance in-situ at bending. While having 1–5% responsivity when exposed to 5–35 ppm ammonia in flat condition, the response is raised generally under increasing strain denoted as the radius of curvature from 10 mm to 4 mm, with a peak value of 2.3% in 5 ppm NH3. Notably, the power consumption of our PPy-graphene sensor could be as low as $17 mumathrm{W}$. This work suggests PPy-graphene hybrid as energy-efficient and high-performance flexible sensor towards electronic skin for environmental monitoring.
二维(2D)材料及其与导电聚合物的结合是高性能气体传感的新兴候选材料,具有理想的机械灵活性。研究外加应变对柔性传感器传感性能的影响具有重要意义。在这项工作中,我们研究了石墨烯和聚吡咯(PPy)的组合作为柔性传感器器件,并探索了它们在弯曲时的原位氨传感性能。在平坦条件下,5 - 35 ppm氨的响应率为1-5%,随着应变的增加(曲率半径从10 mm增加到4 mm),响应率普遍提高,5 ppm NH3的峰值为2.3%。值得注意的是,我们的ppy -石墨烯传感器的功耗可以低至$17 mu mathm {W}$。这项工作表明,ppy -石墨烯混合材料是一种节能、高性能的柔性传感器,可用于环境监测的电子皮肤。
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引用次数: 1
Sinter-free inkjet-printed PEDOT:PSS/WO3/ PEDOT:PSS flexible valency change memory 无烧结喷墨打印PEDOT:PSS/WO3/ PEDOT:PSS柔性变价存储器
Pub Date : 2021-12-12 DOI: 10.1109/nmdc50713.2021.9677487
Mohamed Delfag, R. Katoch, J. Jehn, Y. González, C. Schindler, A. Ruediger
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引用次数: 0
Quantized Domain-Wall Magnetic Tunnel Junction (DW-MTJ) Neural Networks Optimized for Rapid, Energy Efficient Edge Inference 用于快速、高效边缘推断的量化畴壁磁隧道结(DW-MTJ)神经网络优化
Pub Date : 2021-12-12 DOI: 10.1109/nmdc50713.2021.9677536
C. Bennett, Samuel Liu, T. Xiao, Otitoaleke G. Akinola, Alexander J. Edwards, Wesley H. Brigner, Can Cui, Thomas Leonard, Mashid Alamdar, Naimul Hassan, R. Jacobs-Gedrim, J. Friedman, J. Incorvia, M. Marinella
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引用次数: 0
Spectroscopic Analysis of Pulsed Underwater Spark for Nanoparticles Synthesis Using Cu and Mo Electrodes 利用铜和钼电极合成纳米粒子的脉冲水下火花的光谱分析
Pub Date : 2021-12-12 DOI: 10.1109/NMDC50713.2021.9677471
T. Tmenova, F. Valensi, A. Veklich, Y. Cressault, V. Boretskij
Pulsed underwater discharges are used for the synthesis of nanoparticles, through electrode tip vaporization and material condensation. The resulting colloid solution can have applications in biomedical (sterilization) or agriculture (plants fertilizing) field. The plasma formed from vaporized water and electrode material constitutes a key step in the process. This work is dedicated to studying plasma parameters as a function of current and used electrode material. Optical emission spectroscopic diagnostic is used to measure electronic temperature (based on copper or molybdenum lines) and density (based on $mathrm{H}_{alpha}$ and $mathrm{H}_{beta}$ lines). The setup allows spatially resolved study over the discharge cross-section. Results show that with molybdenum the core temperature is 30 to 90 % higher but the radial gradient is stronger when compared to copper. Electron density is also twice higher with molybdenum electrodes. High speed imaging confirms that with this metal the spark light intensity is much stronger and the formed cavitation bubble is larger. These results can be explained by the lower thermal conductivity of molybdenum electrodes, leading to a more energetic discharge.
脉冲水下放电通过电极尖端汽化和材料冷凝来合成纳米颗粒。所得胶体溶液可应用于生物医学(杀菌)或农业(植物施肥)领域。由蒸发的水和电极材料形成的等离子体是该过程的关键步骤。这项工作致力于研究等离子体参数作为电流和所用电极材料的函数。光学发射光谱诊断用于测量电子温度(基于铜或钼线)和密度(基于$mathrm{H}_{alpha}$和$mathrm{H}_{beta}$线)。该装置允许对放电截面进行空间分辨研究。结果表明:含钼合金芯温为30 ~ 90℃ % higher but the radial gradient is stronger when compared to copper. Electron density is also twice higher with molybdenum electrodes. High speed imaging confirms that with this metal the spark light intensity is much stronger and the formed cavitation bubble is larger. These results can be explained by the lower thermal conductivity of molybdenum electrodes, leading to a more energetic discharge.
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引用次数: 0
Formation of Nano-Tree and Nano-Ring Structures from Au-Si-Ge Eutectic Solids 从Au-Si-Ge共晶固体中形成纳米树和纳米环结构
Pub Date : 2021-12-12 DOI: 10.1109/nmdc50713.2021.9677476
G. R. Suwito, Weizheng Wang, N. Quitoriano
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引用次数: 1
Contact Modulation Using Pulsed Thermal Annealing in 2-Dimensional Semiconductors 二维半导体的脉冲热退火接触调制
Pub Date : 2021-12-12 DOI: 10.1109/NMDC50713.2021.9677549
Olaiyan Alolaiyan, Abrar S. Alhazmi, Saeed Alghamdi, Faisal Alamri, Khalid Alhamdan, Awsaf Alsulami, Moh. R. Amer
2-Dimensional (2D) materials have been the subject of intensive research for electronic and photonic applications. Yet, the realization of a “good” ohmic contact with 2D materials is still a major hurdle that requires focused investigations. Metal deposition methods have proven to alter the electronic behavior of 2D materials, which can introduce defects and opens scattering paths for carriers. Here, we demonstrate new technique that can modulate contact resistance of the 2D material with the source and drain electrodes using MoS2 transistors. Exfoliated 2D Nanosheets are micro-aligned and deposited on prefabricated metal electrodes. Before any treatment, devices show poor electrical performance with high device resistance which is caused by weak contact between the 2D nanosheet and the metal electrodes. However, after applying a pulsed thermal annealing treatment with a short time interval, we notice a remarkable enhancement in $IV_{ds}$ and $IV_{gs}$ properties. For MoS2 transistors, we notice the maximum enhancement occurring after the first treatment. Our treatment can be a promising technique to create high performance electronics for device applications.
二维(2D)材料已成为电子和光子应用研究的热点。然而,实现与二维材料的“良好”欧姆接触仍然是一个主要障碍,需要集中研究。金属沉积方法已经被证明可以改变二维材料的电子行为,这可能会引入缺陷并打开载流子的散射路径。在这里,我们展示了一种新的技术,可以用二硫化钼晶体管调制二维材料的源极和漏极的接触电阻。剥落的二维纳米片被微排列并沉积在预制金属电极上。在任何处理之前,器件表现出较差的电性能和较高的器件电阻,这是由于二维纳米片与金属电极之间的弱接触造成的。然而,经过短时间间隔的脉冲热退火处理后,我们注意到$IV_{ds}$和$IV_{gs}$的性能显著增强。对于二硫化钼晶体管,我们注意到最大的增强发生在第一次处理之后。我们的处理方法可以成为一种有前途的技术,为设备应用创造高性能电子产品。
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引用次数: 0
Direct Electrodeposition of InSb Devices on Silicon InSb器件在硅上的直接电沉积
Pub Date : 2021-12-12 DOI: 10.1109/NMDC50713.2021.9677527
Katarzyna E Hnida-Gut, M. Sousa, K. Moselund, H. Schmid
Electronic devices based on inexpensive Si technology by far dominate the market for data processing, imaging as well as sensing devices today and in the foreseeable future. Nevertheless, non-Si semiconductors are gaining significant momentum in specialized fields where it is motivated by performance metrics considerably surpassing that of Si. These include wide bandgap semiconductors (GaN) for power electronics and III-Vs (InSb, InGaAs, AlSb, etc.) for sensing and high-speed electronics. Therefore, a large economic potential could result if these two material platforms could seamlessly merge. However, technological difficulties challenge the integration of foreign materials directly on Si due to the crystal lattice, thermal and polarity mismatch leading to the large density of defects, detrimental to most applications. This work addresses this challenge demonstrating direct electrodeposition of indium antimonide on Si in defined geometries by an up-scalable and environmentally friendly aqueous solution process. We have evaluated several electrochemical deposition conditions with particular attention to stability and reproducibility of the process as well as an evaluation of the best electrode configuration. Building on these results, we show that prefabricated hollow template structures of micro- and sub-micron dimensions, each containing a local embedded electrode can be successfully filled with electrodeposited InSb resulting in well-defined device structures on Si. This combines the advantages of high-speed low-cost electrodeposition with the increased control achievable using templates.
目前和可预见的未来,基于廉价硅技术的电子设备在数据处理、成像和传感设备市场上占据主导地位。然而,非硅半导体在特殊领域获得了显著的动力,其性能指标大大超过了硅。其中包括用于电力电子的宽带隙半导体(GaN)和用于传感和高速电子的iii - v (InSb, InGaAs, AlSb等)。因此,如果这两种材料平台能够无缝融合,将产生巨大的经济潜力。然而,由于晶格、热和极性不匹配导致缺陷密度大,对大多数应用不利,因此直接在Si上集成外来材料面临技术困难。这项工作解决了这一挑战,通过一种可扩展的、环保的水溶液工艺,证明了锑化铟在硅上的直接电沉积具有确定的几何形状。我们评估了几种电化学沉积条件,特别注意该过程的稳定性和可重复性,以及对最佳电极配置的评估。在这些结果的基础上,我们展示了预制的微微米和亚微米尺寸的空心模板结构,每个模板都包含一个局部嵌入电极,可以成功地用电沉积的InSb填充,从而在Si上形成定义良好的器件结构。这结合了高速低成本电沉积的优点和使用模板可实现的更高控制。
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引用次数: 2
Competing Crystallization in Multi-ion Perovskites 多离子钙钛矿的竞争结晶
Pub Date : 2021-12-12 DOI: 10.1109/NMDC50713.2021.9677546
M. Saidaminov
To reach their impressive power conversion efficiencies, perovskite solar cells have benefited from extensive empirical optimization. Major progress came from combinatorial optimization of perovskite compositions that now contain fully six or more components, e.g. Cs, MA, FA, Pb, I, Br, and others [1]. Unfortunately, the lack of understanding of the precise role of each component limits further progress in this now-exponentially-growing combinatorial space. Using ultrafast spatio-temporal imaging of carrier diffusion, we discovered that the carrier diffusivity is independent of composition in perovskite single crystals [2]. It is exclusively in polycrystalline thin films that different compositions play a crucial role in influencing carrier diffusivity and lifetime. Specifically, we found that in the stable cesium-formamidinium perovskite, perovskite films crystallize inhomogeneously: they produce grains whose cores have a lower bandgap, and whose shells have a higher bandgap. We then use this knowledge and find that the incorporation of a small amount of methylammonium homogenizes crystallization. This flattens the energetic landscape for carriers to move among grains. The proposed mechanism, through which the perovskite grain formation governs carrier transport, clarifies the widely-observed - but previously-unexplained - beneficial role of mixing.
为了达到令人印象深刻的能量转换效率,钙钛矿太阳能电池受益于广泛的经验优化。主要的进展来自钙钛矿组合物的组合优化,现在钙钛矿组合物包含了六种或更多的成分,如Cs、MA、FA、Pb、I、Br等。不幸的是,缺乏对每个组成部分的精确作用的理解限制了在这个现在呈指数增长的组合空间中的进一步发展。利用载流子扩散的超快时空成像,我们发现载流子扩散率与钙钛矿单晶[2]的组成无关。只有在多晶薄膜中,不同的成分对载流子的扩散率和寿命起着至关重要的作用。具体来说,我们发现在稳定的铯-甲脒钙钛矿中,钙钛矿薄膜结晶不均匀:它们产生的颗粒核具有较低的带隙,而其壳具有较高的带隙。然后我们利用这一知识,发现少量甲基铵的加入使结晶均匀化。这使得运载者在谷物之间移动的能量景观变得平坦。提出的机制,通过钙钛矿颗粒形成控制载流子运输,澄清了广泛观察-但以前无法解释-混合的有益作用。
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引用次数: 0
Tunable Multiferroics for Reconfigurable RF System Packages 可调谐多铁质可重构射频系统封装
Pub Date : 2021-12-12 DOI: 10.1109/NMDC50713.2021.9677517
Pawan Gaire, Veeru Jaiswal, S. Y. B. Sayeed, J. Volakis, M. Pulugurtha, S. Bhardwaj
Electric and magnetic properties of multiferroics can be conveniently tuned with applied electric and magnetic fields. Such tunability provides multiple design options for reconfigurable antennas and smart shielding applications and is thus of high interest. Dielectric tuning is commonly achieved with electric fields, which is more suitable with thin-films as they need lower voltages. For thick RF dielectrics that are used in antennas and Frequency Selective Surfaces (FSS), tuning requires 100s of Volts. To address this problem, we propose current-driven tuning of permittivity with integrated coils under the multiferroic. Tunable dielectric properties in nanostructured titanate paraelectrics are investigated through simulations by coupling them with magnetostrictive layers. In parallel, cosintered ferrite and paraelectric dielectrics are characterized for their tunability. The change in dielectric constant with magnetic fields is analyzed through multiphysics COMSOL simulations. Permittivity tuning is modeled with different coil currents. Applications in tunable FSS is demonstrated with such dielectric tuning.
在外加电场和磁场的作用下,多铁体的电、磁特性可以很方便地调谐。这种可调性为可重构天线和智能屏蔽应用提供了多种设计选择,因此备受关注。介质调谐通常是通过电场来实现的,这更适合于薄膜,因为它们需要更低的电压。对于天线和频率选择表面(FSS)中使用的厚RF介质,调谐需要100伏。为了解决这个问题,我们提出了在多铁性下使用集成线圈进行电流驱动的介电常数调谐。通过与磁致伸缩层耦合的模拟研究了纳米钛酸盐类电材料的可调介电性能。同时,共感铁氧体和亲电介质具有可调性。通过COMSOL多物理场模拟,分析了介质常数随磁场的变化。用不同线圈电流对介电常数调谐进行建模。用这种介电调谐方法演示了在可调谐FSS中的应用。
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引用次数: 3
期刊
2021 IEEE 16th Nanotechnology Materials and Devices Conference (NMDC)
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