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Morphological and chemical evolution of monocrystalline porous germanium over time in various storage environments 单晶多孔锗在不同储存环境中的形态和化学演变
IF 2.8 Q2 ENGINEERING, ELECTRICAL & ELECTRONIC Pub Date : 2024-07-20 DOI: 10.1016/j.mne.2024.100274
Valentin Daniel , Jérémie Chretien , Sonia Blais , Jinyoun Cho , Kristof Dessein , Gwenaelle Hamon , Abderraouf Boucherif , Maxime Darnon

Mesoporous germanium (MP-Ge) emerges as a very appealing material for many applications such as anode material for Lithium-Ion batteries due to it high specific area and large void spaces or, in optoelectronics as sacrificial layer for III-V materials growth and detachment, allowing notably several uses of a single Ge substrate. These porous nanostructures are distinguished by a large specific surface area and are prone to degradation with time due to exposure to the environment. To understand and be able to reduce this effect, we studied the chemical and morphological evolution of porous germanium layers under various ambient storage conditions for 3 months to identify the main parameters responsible for material degradation. This study demonstrates that the ambient air environment leads to the growth of native oxide, leading to major morphology changes. Scanning electrons microscope (SEM) showed the formation of clusters and the enlargement of the pores after 90 days. These structural modifications are caused by the oxidation of Ge, and more specifically by the creation of GeO2 matrices due to the synergy of dioxygen (O2) and humidity (H2O(g)). The energy brought by light can exacerbate these phenomena and thus accelerate the degradation rate of the pore morphology. Based on these experimental results, we propose efficient solutions to limit the GeO2 proportions and the clusters' appearance, by storing them under a dry neutral atmosphere (Ar) or by adding a hydrogen halide pre-treatment (10s 1% HBr solution).

介孔锗(MP-Ge)因其高比表面积和大空隙,在许多应用领域成为一种极具吸引力的材料,例如用作锂离子电池的负极材料,或在光电子学中用作 III-V 材料生长和分离的牺牲层,从而使单一的 Ge 衬底具有多种用途。这些多孔纳米结构的特点是比表面积大,暴露在环境中容易随时间退化。为了了解并减少这种影响,我们研究了多孔锗层在各种环境储存条件下 3 个月的化学和形态演变,以确定导致材料降解的主要参数。这项研究表明,环境空气环境会导致原生氧化物的生长,从而导致形态发生重大变化。扫描电子显微镜(SEM)显示,90 天后形成了团块并扩大了孔隙。这些结构变化是由 Ge 氧化引起的,更具体地说,是由于二氧(O2)和湿度(H2O(g))的协同作用产生了 GeO2 基质。光带来的能量会加剧这些现象,从而加快孔隙形态的退化速度。根据这些实验结果,我们提出了限制 GeO2 比例和晶簇出现的有效解决方案,即在干燥的中性气氛(Ar)下储存或添加卤化氢预处理(10s 1%HBr溶液)。
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引用次数: 0
Rapid and versatile, micro-patterning and functionalization of complex structures on ultra-thin and flexible polymeric substrates 在超薄柔性聚合物基底上快速、多用途地对复杂结构进行微图案化和功能化处理
IF 2.8 Q2 ENGINEERING, ELECTRICAL & ELECTRONIC Pub Date : 2024-07-10 DOI: 10.1016/j.mne.2024.100273
E. Cunaj , E. Gogolides , A. Tserepi , K. Ellinas

Microscale patterning on flexible substrates is important in many applications such as in wearable sensors and microfluidics-based diagnostics, therefore low-cost fabrication methods which are scalable and amenable to mass production have attracted the interest of many companies and research groups. Dry film resists (DFRs) are commercially available materials with properties compatible with their implementation on flexible substrates to cover a wide range of applications, which also offer environmental and sustainability benefits due to the low waste generation compared to the liquid resists. However, there are limited detailed reports in the literature regarding the use of DFRs for the fabrication of microfluidic channels or other micropatterns (i.e., posts) on thin and flexible substrates. Herein we present in detail the fabrication of: a) microfluidic channels of width ranging from 50 μm up to 800 μm, and depth ranging from 30 μm up to 270 μm and b) square posts 80 μm × 80 μm in size and 30 μm in height. Particularly, our method enables the fabrication of ultra-deep microchannels (depth > 250 μm), highly ordered post arrays over large area (appr. 60 cm2), as well as complex designs with hierarchical scale features (80 μm posts inside 800 μm microchannels or micro-nanotexturing inside microchannels) on ultra-thin flexible substrates. To demonstrate the versatility of the method, three different DFRs were used on ultra-thin (30 μm), flexible, single-sided copper-clad polyimide substrates. It is also demonstrated that DFRs can be effectively modified using plasma etching to tune the surface wetting properties towards applications such as pumpless capillary action, where such functionality is required.

在可穿戴传感器和基于微流控技术的诊断等许多应用中,柔性基底上的微米级图案化都非常重要,因此,可扩展且适合大规模生产的低成本制造方法吸引了许多公司和研究团体的兴趣。干膜抗蚀剂(DFRs)是可在市场上买到的材料,其特性适合在柔性基底上使用,应用范围广泛,与液态抗蚀剂相比,产生的废料少,具有环保和可持续发展的优势。然而,文献中关于使用 DFR 在薄而柔性的基底上制造微流体通道或其他微图案(即柱)的详细报道并不多。在此,我们将详细介绍:a) 宽度从 50 μm 到 800 μm,深度从 30 μm 到 270 μm 的微流体通道的制造方法;b) 尺寸为 80 μm × 80 μm、高度为 30 μm 的方形柱子的制造方法。特别是,我们的方法可以在超薄柔性基底上制造超深微通道(深度为 250 微米)、大面积高度有序的柱阵列(约 60 平方厘米),以及具有分层尺度特征的复杂设计(800 微米微通道内的 80 微米柱或微通道内的微纳米纹理)。为了证明该方法的多功能性,在超薄(30 μm)、柔性、单面覆铜聚酰亚胺基底上使用了三种不同的 DFR。研究还表明,可利用等离子刻蚀技术对 DFR 进行有效改性,以调整其表面润湿特性,使其适应无泵毛细管作用等需要此类功能的应用。
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引用次数: 0
PEDOT:PSS deposition in OECTs: Inkjet printing, aerosol jet printing and spin coating PEDOT:PSS 在 OECTs 中沉积:喷墨打印、气溶胶喷射打印和旋涂
IF 2.8 Q2 ENGINEERING, ELECTRICAL & ELECTRONIC Pub Date : 2024-07-10 DOI: 10.1016/j.mne.2024.100272
Giorgia Rinaldi , Davide Vurro , Martina Cicolini , Jovana Babic , Aris Liboà , Giuseppe Tarabella , Pasquale D'Angelo , Simone L. Marasso , Matteo Cocuzza , Lorenzo Vigna , Fabrizio C. Pirri , Matteo Parmeggiani

As the world moves towards integrating new functionalities into everyday objects, the demand for diverse substrates grows, making additive manufacturing an invaluable tool. Organic electronic materials have played a major role in this transition thanks to their excellent electronic and mechanical properties, adaptability and solution processability.

The aim of this study is to compare spin coating, inkjet printing (IJP), and aerosol jet printing (AJP) for applying poly(3,4-ethylenedioxythiophene) polystyrene sulfonate (PEDOT:PSS) as the channel material in organic electrochemical transistors (OECTs). This work investigates the often-overlooked impact of deposition techniques on the electrical performance of OECTs. Spin coating has been analysed as a reference technique, while AJP and IJP are addressed as promising pathways towards fully printed OECTs.

The normalized transconductance and Ion/Ioff ratio have been analysed as figures of merit for this study. AJP devices have shown the best performance, displaying a normalized transconductance of 885 S∙nm and an Ion/Ioff ratio around 103. The spin coated OECTs showed a slightly lower normalized transconductance (740 S∙nm) and much lower Ion/Ioff ratio in the order of 101. Last, IJP exhibited a transconductance of 433 S∙nm and a Ion/Ioff ratio in the order of 102.

This work could be beneficial for a wide range of applications, adding an additional degree of freedom to the tunability of the OECT channel properties. It also opens the discussion for more comprehensive studies on the films from a materials perspective.

随着世界朝着将新功能集成到日常物品中的方向发展,对各种基材的需求也在不断增长,这使得快速成型制造成为一种宝贵的工具。本研究旨在比较自旋涂层、喷墨打印(IJP)和气溶胶喷射打印(AJP)在有机电化学晶体管(OECTs)中应用聚(3,4-亚乙二氧基噻吩)聚苯乙烯磺酸盐(PEDOT:PSS)作为通道材料的效果。这项研究探讨了沉积技术对有机电化学晶体管电气性能的影响,而这一影响往往被忽视。旋转涂层作为一种参考技术进行了分析,而 AJP 和 IJP 则作为实现完全印刷 OECTs 的可行途径。AJP 器件表现出最佳性能,显示出 885 S∙nm 的归一化跨导和 103 左右的离子/离子交换率。自旋涂层 OECT 显示出略低的归一化跨导(740 S∙nm)和低得多的离子/离子关断比(101)。最后,IJP 显示出 433 S∙nm 的跨导率和 102 数量级的离子/离子关断比。这项工作可能有利于广泛的应用,为 OECT 沟道特性的可调性增加了额外的自由度。这项研究还为从材料角度对薄膜进行更全面的研究开辟了讨论空间。
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引用次数: 0
3D printed diffractive optical elements for rapid prototyping 用于快速原型制作的 3D 打印衍射光学元件
IF 2.8 Q2 ENGINEERING, ELECTRICAL & ELECTRONIC Pub Date : 2024-07-02 DOI: 10.1016/j.mne.2024.100270
Daniel Fan , Carlas S. Smith , Ranjith R. Unnithan , Sejeong Kim

A rapid and robust method to fabricate transmission diffractive optical elements in the visible wavelengths is presented. By additive manufacturing of a polymeric photo-resin using 2-photon lithography followed by encasing of the structure in another resin with similar refractive index, the height of the structure can be made much larger, thus trading-off fabrication height for refractive index difference of the two materials. After adjusting for resin shrinkage, different diffractive optical element designs including an m = 1 vortex plate, and Laguerre-Gaussian beams with azimuthal and radial indices of (1,1), (1,2), and (2,1) were demonstrated. Experimental results show intensity patterns matching that of simulations, including size and features, although some aberration was observed, possibly due to fabrication tolerance errors or beam misalignment. This technique adds to the toolkit of micro-optics fabrication methods using additive manufacturing and 3D printing, and it would be beneficial for rapid prototyping and integration with miniaturised systems.

本文介绍了一种快速、稳健的方法,用于制造可见光波段的透射衍射光学元件。通过使用双光子光刻技术对聚合物光敏树脂进行增材制造,然后将结构包裹在折射率相似的另一种树脂中,可以使结构的高度大大增加,从而以两种材料的折射率差异来权衡制造高度。在对树脂收缩进行调整后,我们展示了不同的衍射光学元件设计,包括 m = 1 涡流板,以及方位角和径向折射率分别为 (1,1)、(1,2) 和 (2,1) 的拉盖尔-高斯光束。实验结果表明,强度模式(包括尺寸和特征)与模拟结果一致,但也观察到一些畸变,这可能是由于制造公差误差或光束偏差造成的。这项技术为使用增材制造和三维打印技术的微型光学制造方法增添了新的工具包,有利于快速原型制造和与微型化系统集成。
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引用次数: 0
Metallization of polyetherimide with 3D structures by supercritical carbon dioxide-assisted electroless NiP plating 通过超临界二氧化碳辅助无电解NiP电镀实现具有三维结构的聚醚酰亚胺的金属化
IF 2.8 Q2 ENGINEERING, ELECTRICAL & ELECTRONIC Pub Date : 2024-07-02 DOI: 10.1016/j.mne.2024.100271
Ami Iwasaki , Tomoyuki Kurioka , Po-Wei Cheng , Chun-Yi Chen , Tso-Fu Mark Chang , Kei Takase , Hiroshi Ishihata , Masato Sone

Polyetherimide (PEI) with 3-dimensional (3D) structures is a promising material for applications in electronic devices because of its numerous attractive properties. In the applications of PEI, the low electrical conductivity is often a shortcoming. The electrical conductivity can be improved by a metallization process. Electroless plating is a common metallization process for polymeric materials; however, conventional electroless plating process scarcely provides the metallized PEI. In this work, we overcome this limitation by a supercritical carbon dioxide (scCO2)-assisted electroless NiP plating process. This scCO2-assisted electroless NiP plating allows metallization of PEI with 3D structures and realizes a low electrical resistance suitable for practical use in the electronic devices.

具有三维(3D)结构的聚醚酰亚胺(PEI)因其众多吸引人的特性,在电子设备中是一种很有应用前景的材料。在 PEI 的应用中,低导电性往往是一个缺点。可以通过金属化工艺来提高导电性。无电解电镀是高分子材料常用的金属化工艺,但传统的无电解电镀工艺几乎无法提供金属化的 PEI。在这项工作中,我们采用超临界二氧化碳(scCO2)辅助无电解镀镍工艺克服了这一限制。这种由 scCO2 辅助的无电解镀镍工艺可实现具有三维结构的 PEI 金属化,并具有适合电子设备实际使用的低电阻。
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引用次数: 0
Superhydrophobic and oleophobic Nylon, PES and PVDF membranes using plasma nanotexturing: Empowering membrane distillation and contributing to PFAS free hydrophobic membranes 利用等离子纳米挤压技术制造超疏水性和疏油性尼龙、聚醚砜和聚偏二氟乙烯膜:增强膜蒸馏能力,促进形成不含 PFAS 的疏水膜
IF 2.8 Q2 ENGINEERING, ELECTRICAL & ELECTRONIC Pub Date : 2024-07-02 DOI: 10.1016/j.mne.2024.100269
Eleftherios Manouras , Dimosthenis Ioannou , Angelos Zeniou , Andreas Sapalidis , Evangelos Gogolides

As freshwater demand is constantly increasing, water purification via membrane distillation (MD) emerges as a promising water production technology, especially when combined with the use of superhydrophobic membranes. Here, following our previous work [1] we extend our universal, environmentally friendly, plasma nanotexturing and hydrophobization technology for rendering practically any type of membrane superhydrophobic and oleophobic. Thus, we render three commercial porous membranes superhydrophobic, namely, polyvinylidene (PVDF 0.45 μm) (initially hydrophobic), polyethersulfone (PES 1.20 μm) and nylon (NY 1.20 μm) (both initially hydrophilic). We demonstrate superhydrophobic, superoleophobic (down to 40mn/m surface tension) and oleophobic properties (down to 30mN/m surface tension) for PVDF, PES and Nylon membranes thus paving the way for their use with low surface tension waste streams. Moreover, the technology presented herein not only improves existing hydrophobic membranes but may lead to elimination of the use of Teflon-like fluorinated hydrophobic membranes altogether in the future, thereby contributing to the PFAS (Per and Poly Fluoro Alkyl Substances) and Teflon-like membrane use reduction. We subsequently evaluated the performance of the treated membranes in direct contact membrane distillation (DCMD) for desalination of sea-like water (35 g/L NaCl). All membranes showed enhanced water flux with an increase of >13% compared to the pristine hydrophobic PVDF membranes for at least 2 h of continuous operation, with salt rejection exciding 99.99%.

随着淡水需求的不断增加,通过膜蒸馏(MD)进行水净化已成为一种前景广阔的水生产技术,尤其是在结合使用超疏水膜的情况下。在这里,继我们之前的工作[1]之后,我们扩展了我们的通用、环保、等离子纳米挤压和疏水技术,使几乎所有类型的膜都具有超疏水性和疏油性。因此,我们对三种商用多孔膜进行了超疏水处理,即聚偏二氟乙烯(PVDF 0.45 μm)(最初为疏水性)、聚醚砜(PES 1.20 μm)和尼龙(NY 1.20 μm)(最初均为亲水性)。我们展示了 PVDF、PES 和尼龙膜的超疏水性、超疏油性(表面张力低至 40mn/m)和疏油性(表面张力低至 30mN/m),从而为它们在低表面张力废物流中的应用铺平了道路。此外,本文介绍的技术不仅能改进现有的疏水膜,还可能在未来完全淘汰特氟龙类氟化疏水膜的使用,从而为减少 PFAS(全氟烷基和聚氟烷基物质)和特氟龙类膜的使用做出贡献。随后,我们评估了经过处理的膜在直接接触膜蒸馏(DCMD)中用于海水(35 克/升 NaCl)脱盐的性能。与原始疏水性 PVDF 膜相比,所有膜在连续运行至少 2 小时后,水通量均有所提高,增幅达 13%,盐分去除率超过 99.99%。
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引用次数: 0
Moving toward autonomous manufacturing by accelerating hydrodynamic fabrication of microstructures using deep neural networks 利用深度神经网络加速微结构的流体力学制造,向自主制造迈进
IF 2.8 Q2 ENGINEERING, ELECTRICAL & ELECTRONIC Pub Date : 2024-06-30 DOI: 10.1016/j.mne.2024.100268
Nicholus R. Clinkinbeard, Nicole N. Hashemi

Manufacturing of microstructures using a microfluidic device is a largely empirical effort due to the multi-physical nature of the fabrication process. As such, in moving toward autonomous manufacturing, models are desired that will predict microstructure attributes (e.g., size, porosity, and stiffness) based on known inputs, such as sheath and core fluid flow rates. Potentially more useful is the prospect of inputting desired microfiber features into a design model to extract appropriate manufacturing parameters. In this study, we demonstrate that deep neural networks (DNNs) trained with sparse datasets augmented by synthetic data can produce accurate predictive and design models to accelerate materials development. For our predictive model with known sheath and core flow rates and bath solution percentage, calculated solid microfiber dimensions are shown to be greater than 95% accurate, with porosity and Young's modulus exhibiting greater than 90% accuracy for a majority of conditions. Likewise, the design model is able to recover sheath and core flow rates with 95% accuracy when provided values for microfiber dimensions, porosity, and Young's modulus. As a result, DNN-based modeling of the microfiber fabrication process demonstrates high potential for reducing time to manufacture of microstructures with desired characteristics.

由于制造过程的多物理特性,利用微流体设备制造微结构在很大程度上是一项经验性工作。因此,在实现自主制造的过程中,我们需要能根据已知输入(如鞘液和芯液流速)预测微结构属性(如尺寸、孔隙率和刚度)的模型。将所需的超细纤维特征输入设计模型,以提取适当的制造参数,可能会更有用。在本研究中,我们证明了用合成数据增强的稀疏数据集训练的深度神经网络(DNN)可以生成精确的预测和设计模型,从而加速材料开发。在已知鞘和芯流速以及浴液百分比的情况下,我们的预测模型计算出的固体超细纤维尺寸准确率超过 95%,在大多数条件下,孔隙率和杨氏模量的准确率超过 90%。同样,在提供超细纤维尺寸、孔隙率和杨氏模量值的情况下,设计模型能够以 95% 的准确率恢复鞘和芯的流速。因此,基于 DNN 的超细纤维制造工艺建模在缩短具有所需特性的微结构的制造时间方面具有很大的潜力。
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引用次数: 0
Prospects of nano-lithographic tools for the fabrication of surface-enhanced Raman spectroscopy (SERS) substrates 纳米光刻工具在制造表面增强拉曼光谱(SERS)基底方面的应用前景
Q2 ENGINEERING, ELECTRICAL & ELECTRONIC Pub Date : 2024-06-01 DOI: 10.1016/j.mne.2024.100267
K. Srivastava , H. Le-The , J.J.A. Lozeman , A. van den Berg , W. van der Stam , M. Odijk

The previous decades have seen a massive increase in the research towards reproducible and optimized surface-enhanced Raman spectroscopy (SERS) substrates. While traditional colloidal synthesis methods have commonly been used for SERS substrate fabrication, they lack reproducibility hindering their usage for many applications. The need for reproducible nanostructures showing high orders of enhancement factors has brought about a shift in the methods one can use to fabricate SERS nanostructures. Lithographic techniques have thus piqued the interest of researchers as a viable option for SERS substrate fabrication. Not only do they offer high enhancement factors and reproducible nanostructures, they also provide the ability to fabricate nanostructures with many different geometries, shapes, sizes and periodicities. Some of the most established lithographic techniques include electron beam lithography, nanosphere lithography, laser interference lithography and many more. This review discusses established lithographic techniques, such as mentioned above, along with other upcoming lithographic techniques to understand the principles and the methodology behind them. A deep understanding of how various parameters can influence the nanostructure fabrication and thereby influence the SERS enhancement is developed. A detailed description of how these nanostructures can be fabricated is also provided for better insight. In addition, strengths and limitations of each method are discussed in detail. Lastly, we also discuss the applicability of SERS substrates for commercial applications comparing the performance of chemical synthesis routes and lithography for SERS substrate fabrication. This review serves as a base to understand the concept and application of SERS from a microfabrication perspective.

在过去的几十年里,对可重现和优化的表面增强拉曼光谱(SERS)基底的研究有了大幅增长。虽然传统的胶体合成方法通常用于 SERS 基底的制造,但它们缺乏可重复性,阻碍了它们在许多应用中的使用。对显示高阶增强因子的可重现纳米结构的需求,带来了 SERS 纳米结构制造方法的转变。因此,平版印刷技术作为一种可行的 SERS 基底制造方法,引起了研究人员的兴趣。平版印刷技术不仅能提供高增强因子和可重现的纳米结构,还能制造出具有多种不同几何形状、大小和周期性的纳米结构。一些最成熟的光刻技术包括电子束光刻、纳米层光刻、激光干涉光刻等。本综述将讨论上述成熟的光刻技术以及其他即将出现的光刻技术,以了解这些技术背后的原理和方法。深入了解各种参数如何影响纳米结构的制造,从而影响 SERS 的增强。此外,还详细介绍了如何制造这些纳米结构,以便更好地理解。此外,还详细讨论了每种方法的优势和局限性。最后,我们还讨论了 SERS 基底在商业应用中的适用性,比较了用于 SERS 基底制造的化学合成路线和光刻法的性能。本综述可作为从微细加工角度理解 SERS 概念和应用的基础。
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引用次数: 0
UV-curable coatings for energy harvesting applications: Current state-of-the-art and future perspectives 用于能量收集应用的紫外线固化涂层:当前最新技术与未来展望
Q2 ENGINEERING, ELECTRICAL & ELECTRONIC Pub Date : 2024-06-01 DOI: 10.1016/j.mne.2024.100266
Donatella Duraccio , Pier Paolo Capra , Giulio Malucelli

Generally speaking, energy harvesting is an up-to-date technology that describes the possibility of capturing small amounts of energy (thermal, solar, or mechanical) from the surroundings and storing them as electrical energy for later uses when needed. Among the energy harvesting systems, the use of piezoelectric thin films and coatings is gaining increasing interest from both the academic and industrial communities, as these systems allow for the design and development of micro- and nano-scale devices, thanks to the possibility of being micromachined and to the added functionality offered by the electromechanical coupling. These peculiarities justify their use for different applications, ranging from high energy density harvesters to high sensitivity sensors, and even low power consumption and large displacement actuators. Further, the current focus of the research on piezoelectric energy harvesting coatings is shifting from fully inorganic to hybrid organic-inorganic (i.e., composite) systems, as the latter can offer higher flexibility (i.e., lower stiffness), making them more sensitive to small vibrations and therefore suitable for these specific harvesting conditions. In this regard, photoinduced polymerization (the so-called “UV-curing”) has become a suitable and reliable technique for the manufacturing of piezoelectric composite systems, as it is a solvent-free approach that allows for transforming a liquid mixture of monomers/oligomers into a solid 3D network in a few seconds, with a very limited energy consumption and a very high conversion. Besides, as the UV-curing process is very fast, the dispersed ceramic piezoelectric phase is not prone to settle down in the liquid resin, hence ensuring its homogeneous distribution within the polymer network after curing and better piezoelectric performance. The present review aims to provide the reader with an up-to-date overview of UV-curable coatings for piezoelectric energy harvesting purposes, highlighting their potential and piezoelectric features; further, some perspectives about possible future developments will be proposed.

一般来说,能量收集是一种最新技术,它描述了从周围环境中捕获少量能量(热能、太阳能或机械能)并将其储存为电能以供日后需要时使用的可能性。在能量收集系统中,压电薄膜和涂层的使用越来越受到学术界和工业界的关注,因为这些系统可以设计和开发微型和纳米级设备,这要归功于微机械加工的可能性和机电耦合提供的附加功能。这些特性证明了它们可用于不同的应用领域,从高能量密度采集器到高灵敏度传感器,甚至是低功耗和大位移执行器。此外,目前压电能量收集涂层的研究重点正从完全无机转向有机-无机混合(即复合)系统,因为后者可以提供更高的灵活性(即更低的刚度),使其对微小振动更加敏感,因此适用于这些特定的收集条件。在这方面,光诱导聚合(即所谓的 "紫外线固化")已成为制造压电复合材料系统的一种合适而可靠的技术,因为它是一种无溶剂方法,可在几秒钟内将单体/配体的液态混合物转化为固态三维网络,且能耗非常有限,转化率非常高。此外,由于紫外固化过程非常快,分散的陶瓷压电相不易沉淀在液态树脂中,因此可确保其在固化后均匀分布在聚合物网络中,从而获得更好的压电性能。本综述旨在向读者介绍用于压电能量收集目的的紫外固化涂层的最新概况,重点介绍其潜力和压电特性;此外,还将对未来可能的发展提出一些展望。
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引用次数: 0
Characterization of negative tone photoresist mr-EBL 6000.5 for i-line stepper and electron beam lithography for the Intra-Level Mix & Match Approach 用于 i 线步进和电子束光刻的负调光刻胶 mr-EBL 6000.5 在级内混合与匹配方法中的特性分析
Q2 ENGINEERING, ELECTRICAL & ELECTRONIC Pub Date : 2024-06-01 DOI: 10.1016/j.mne.2024.100264
S. Schermer , C. Helke , M. Reinhardt , S. Hartmann , F. Tank , J. Wecker , G. Heldt , A. Voigt , D. Reuter

In this paper the characterization of the mr-EBL 6000.5, which is an epoxy resin based chemically amplified negative tone resist from micro resist technology (Germany, Berlin) for an Intra-Level Mix & Match (ILM&M) approach is presented. The ILM&M approach combined at least two exposure technologies on the same resist layer showing the advantage to resolve patterns of different dimensions with less process steps and short processing time. Since the mr-EBL 6000.5 resist is capable of being sensitive to both electron- and UV-radiation, process parameters for i-line stepper lithography and electron beam lithography (EBL) needs to be investigated to be capable for the ILM&M approach. First, a spin curve and a post exposure bake (PEB) study were applied to find suitable process parameters for both exposure technologies. Furthermore, the minimum feature sizes for both patterning technologies are investigated by using a 500 nm thick resist layer. The impact of small feature sizes near the CD-limit of the used i-line stepper (350 nm) on the resist thickness after the development was investigated in dependence of the PEB. After all parameters were examined, they were combined to be used in the ILM&M.

本文介绍了 mr-EBL 6000.5 的特性,这是一种基于环氧树脂的化学放大负调光刻胶,由德国柏林微光刻胶技术公司生产,采用了层内混合匹配(ILM&M)方法。ILM&M 方法在同一光刻胶层上结合了至少两种曝光技术,具有工艺步骤少、加工时间短的优势,可以解决不同尺寸的图案问题。由于 mr-EBL 6000.5 光刻胶对电子和紫外线辐射都很敏感,因此需要研究 i-line步进光刻和电子束光刻(EBL)的工艺参数,使其能够用于 ILM&M 方法。首先,应用自旋曲线和曝光后烘烤(PEB)研究为两种曝光技术找到合适的工艺参数。此外,通过使用 500 nm 厚的抗蚀层,研究了两种图案技术的最小特征尺寸。在所使用的 i 线步进器的 CD 限值(350 nm)附近的小特征尺寸对显影后抗蚀层厚度的影响与 PEB 有关。在对所有参数进行检查后,将它们组合起来用于 ILM&M。
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Micro and Nano Engineering
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