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Key factors and performance criteria of wearable strain sensors based on polymer nanocomposites 基于聚合物纳米复合材料的可穿戴应变传感器的关键因素和性能标准
IF 2.1 4区 材料科学 Q3 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2023-03-22 DOI: 10.1088/2399-1984/acc6ab
Aliya Zhagiparova, G. Kalimuldina, Abdullatif Lacina Diaby, F. Abbassi, Md. Hazrat Ali, S. Araby
Recently, there has been growing demand for wearable electronic devices/strain sensors in soft robotics, body-health monitoring, human–machine interfaces, and human motion detection. Wearable strain sensors feature fast and multistimuli sensitivity, high flexibility, ultrastretchability, and biocompatibility. Although progress in flexible strain sensors is exponential, the production of wearable sensors faces several challenges, such as reliability and reproducibility. An in-depth understanding of the sensing mechanisms of flexible strain sensors based on’ polymeric nanocomposites is needed to fabricate reliable and reproducible sensors and move from the prototype phase into the industry phase. In this review, types of strain sensors and key parameters such as linearity, gauge factor (sensitivity), hysteresis, and durability are explained in the context of recently published work. In addition, current challenges and perspectives in relation to wearable strain sensors are delineated.
近年来,软机器人、身体健康监测、人机界面和人体运动检测等领域对可穿戴电子设备/应变传感器的需求不断增长。可穿戴应变传感器具有快速和多刺激敏感性,高灵活性,超拉伸性和生物相容性。虽然柔性应变传感器的进展是指数级的,但可穿戴传感器的生产面临着一些挑战,如可靠性和可重复性。深入了解基于聚合物纳米复合材料的柔性应变传感器的传感机制,需要制造可靠且可重复的传感器,并从原型阶段进入工业阶段。在这篇综述中,应变传感器的类型和关键参数,如线性度,测量因子(灵敏度),迟滞和耐久性在最近发表的工作背景下进行了解释。此外,描述了当前与可穿戴应变传感器相关的挑战和前景。
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引用次数: 0
Facile growth of high-yield and -crystallinity vertically aligned carbon nanotubes via a sublimated ferric chloride catalyst precursor 利用升华氯化铁催化剂前驱体制备高产量、高结晶度垂直排列的碳纳米管
IF 2.1 4区 材料科学 Q3 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2023-03-14 DOI: 10.1088/2399-1984/acc43c
H. Goktas, N. Lachman, E. Kalfon-Cohen, Xiaoxue Wang, S. Torosian, K. Gleason, B. Wardle
A facile and effective catalyst deposition process for carbon nanotube (CNT) array growth via chemical vapor deposition using a resistively heated thermal evaporation technique to sublimate FeCl3 onto the substrate is demonstrated. The catalytic activity of the sublimated FeCl3 catalyst precursor is shown to be comparable to the well-studied e-beam evaporated Fe catalyst, and the resulting vertically aligned CNTs (VA-CNTs) have a similar diameter, walls, and defects, as well as improved bulk electrical conductivity. In contrast to standard e-beam-deposited Fe, which yields base-growth CNTs, scanning and transmission electron microscopy and X-ray photoelectron spectroscopy characterizations reveal a tip-growth mechanism for the FeCl3-derived VA-CNT arrays/forests. The FeCl3-derived forests have a lower (∼1/3 less) longitudinal indentation modulus, but higher longitudinal electrical conductivity (greater than twice) than that of the e-beam Fe-grown CNT arrays. The sublimation process to grow high-quality VA-CNTs is a highly facile and scalable process (extensive substrate shape and size, and moderate vacuum and temperatures) that provides a new route to synthesizing aligned CNT forests for numerous applications.
介绍了一种简单有效的碳纳米管(CNT)阵列生长催化剂沉积工艺,该工艺通过化学气相沉积,利用电阻加热热蒸发技术将FeCl3升华到衬底上。经升华的FeCl3催化剂前驱体的催化活性与经过充分研究的电子束蒸发的Fe催化剂相当,并且得到的垂直排列的碳纳米管(VA-CNTs)具有相似的直径、壁和缺陷,并且提高了整体导电性。与标准电子束沉积的Fe不同,扫描电镜和透射电镜以及x射线光电子能谱表征揭示了fecl3衍生的VA-CNT阵列/森林的尖端生长机制。fecl3衍生的碳纳米管阵列具有较低(约1/3)的纵向压痕模量,但比电子束fe生长的碳纳米管阵列具有更高的纵向电导率(大于两倍)。生长高质量VA-CNTs的升华工艺是一种高度简便和可扩展的工艺(衬底形状和尺寸广泛,真空和温度适中),为合成具有多种应用的排列碳纳米管森林提供了一条新途径。
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引用次数: 0
Real-time decoding for fault-tolerant quantum computing: progress, challenges and outlook 容错量子计算的实时解码:进展、挑战和展望
IF 2.1 4区 材料科学 Q3 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2023-02-28 DOI: 10.1088/2399-1984/aceba6
F. Battistel, C. Chamberland, Kauser Johar, Ramon W. J. Overwater, F. Sebastiano, L. Skoric, Yosuke Ueno, M. Usman
Quantum computing is poised to solve practically useful problems which are computationally intractable for classical supercomputers. However, the current generation of quantum computers are limited by errors that may only partially be mitigated by developing higher-quality qubits. Quantum error correction (QEC) will thus be necessary to ensure fault tolerance. QEC protects the logical information by cyclically measuring syndrome information about the errors. An essential part of QEC is the decoder, which uses the syndrome to compute the likely effect of the errors on the logical degrees of freedom and provide a tentative correction. The decoder must be accurate, fast enough to keep pace with the QEC cycle (e.g. on a microsecond timescale for superconducting qubits) and with hard real-time system integration to support logical operations. As such, real-time decoding is essential to realize fault-tolerant quantum computing and to achieve quantum advantage. In this work, we highlight some of the key challenges facing the implementation of real-time decoders while providing a succinct summary of the progress to-date. Furthermore, we lay out our perspective for the future development and provide a possible roadmap for the field of real-time decoding in the next few years. As the quantum hardware is anticipated to scale up, this perspective article will provide a guidance for researchers, focusing on the most pressing issues in real-time decoding and facilitating the development of solutions across quantum, nano and computer science.
量子计算有望解决经典超级计算机在计算上难以解决的实际问题。然而,当前这一代量子计算机受到错误的限制,这些错误可能只能通过开发更高质量的量子比特来部分缓解。因此,量子纠错(QEC)将是确保容错的必要条件。QEC通过循环测量有关错误的综合征信息来保护逻辑信息。QEC的一个重要部分是解码器,它使用该综合征来计算错误对逻辑自由度的可能影响,并提供试探性修正。解码器必须准确,足够快,以跟上QEC周期(例如,超导量子比特在微秒时间尺度上),并具有硬实时系统集成以支持逻辑操作。因此,实时解码是实现容错量子计算和实现量子优势的关键。在这项工作中,我们强调了实现实时解码器所面临的一些关键挑战,同时简要总结了迄今为止的进展。此外,我们对未来的发展进行了展望,并为未来几年的实时解码领域提供了可能的路线图。随着量子硬件规模的扩大,这篇前瞻性文章将为研究人员提供指导,重点关注实时解码中最紧迫的问题,并促进量子、纳米和计算机科学解决方案的发展。
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引用次数: 12
Recent advances in magnetoresistance biosensors: a short review 磁阻生物传感器的研究进展
IF 2.1 4区 材料科学 Q3 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2023-02-16 DOI: 10.1088/2399-1984/acbcb5
Clifton Dey, Parsa Yari, Kai Wu
Recent years have seen the development of spintronic devices and their applications in biomedical areas. Spintronic devices rely on detecting or manipulating a magnetic field, a field to which biological matter is relatively transparent. The recent use of spintronic devices in biomedical areas has included diagnosing diseases such as cancer and cirrhosis, genotyping DNA, point-of-care devices, and flexible electronics. Up to date, most of the spintronic devices in biomedical applications fall into three mainstream types: anisotropic, giant, and tunneling magnetoresistance devices. Each of these has its advantages and drawbacks, which are explored and discussed in this article. The advent of spintronics gives us a new low-power, low-cost, ease-of-manufacture alternative to standard CMOS sensors. The sensitivity of spintronic biosensors has been progressing steadily, expected to increase tremendously in the next few years.
近年来,自旋电子器件及其在生物医学领域的应用得到了发展。自旋电子设备依赖于检测或操纵磁场,生物物质对磁场相对透明。自旋电子设备最近在生物医学领域的应用包括诊断疾病,如癌症和肝硬化、DNA基因分型、定点护理设备和柔性电子设备。到目前为止,生物医学应用中的大多数自旋电子器件可分为三种主流类型:各向异性、巨磁电阻器件和隧道磁阻器件。每种方法都有其优点和缺点,本文对此进行了探讨和讨论。自旋电子学的出现为我们提供了一种新的低功耗、低成本、易于制造的标准CMOS传感器替代品。自旋电子生物传感器的灵敏度一直在稳步发展,预计在未来几年将大幅提高。
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引用次数: 1
Synthesis of AgInS2-ZnS quantum dot/TiO2 nanocomposites as efficient photocatalysts for methylene blue degradation AgInS2-ZnS量子点/TiO2纳米复合材料降解亚甲基蓝的合成
IF 2.1 4区 材料科学 Q3 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2023-01-31 DOI: 10.1088/2399-1984/acb7b7
Nomfundo Ruth Lushaba, S. Parani, Rodney Maluleke, Gracia it Mwad Mbaz, O. Oluwafemi
Photocatalytic degradation has been demonstrated to be an efficient and eco-friendly method for the removal of dye pollutants. Herein, we report the synergetic effect of glutathione (GSH)-capped AgInS2-ZnS (AIS-ZnS) core–shell quantum dots (QDs) and titanium dioxide (TiO2) as a novel nanocomposite for the efficient photocatalytic treatment of methylene blue (MB). The AIS-ZnS core–shell QDs and the corresponding QD/TiO2 nanocomposites were synthesized directly in an aqueous medium followed by annealing. The optical properties of the AIS-ZnS core–shell QDs showed strong yellow photoluminescence, which decreased gradually with the addition of TiO2. Fourier transform infrared (FTIR) spectroscopy confirmed the GSH capping on the QDs and nanocomposites. X-ray diffraction and transmission electron microscopy revealed the nanocrystalline nature and shape of the as-synthesized materials and showed the integration of the QDs (3.9 nm) on the TiO2 particles after annealing. These materials were then investigated as a photocatalyst for MB degradation using visible light irradiation. The effect of TiO2 content in the catalyst, calcination, photoirradiation period, catalyst dose, and initial MB concentration on photodegradation of MB was studied. The results indicated that the AIS-ZnS QD/TiO2 nanocomposite exhibited better photodegradation performance compared to AIS-ZnS QDs and TiO2. The increasing TiO2 concentration in the nanocomposite also enhanced MB degradation efficiency (up to 99%). The kinetics of MB degradation follows a pseudo-first-order process. The prepared AIS-ZnS QD/TiO2 nanocomposite would serve as an effective and eco-friendly photocatalyst for MB degradation.
光催化降解已被证明是一种高效、环保的去除染料污染物的方法。本文报道了谷胱甘肽(GSH)包封的AgInS2-ZnS (AIS-ZnS)核壳量子点(QDs)与二氧化钛(TiO2)作为一种新型纳米复合材料的协同作用,用于亚甲基蓝(MB)的高效光催化处理。在水介质中直接合成了AIS-ZnS核壳量子点和相应的量子点/TiO2纳米复合材料。AIS-ZnS核壳量子点的光学性质表现为强黄色光致发光,随TiO2的加入逐渐减弱。傅里叶变换红外光谱(FTIR)证实了GSH在量子点和纳米复合材料上的封盖作用。x射线衍射和透射电子显微镜显示了合成材料的纳米晶性质和形状,并显示了退火后TiO2粒子上的量子点(3.9 nm)的集成。然后研究了这些材料在可见光照射下作为光催化剂降解MB。研究了催化剂中TiO2含量、煅烧程度、光照射时间、催化剂剂量、初始MB浓度等因素对MB光降解的影响。结果表明,与AIS-ZnS QD和TiO2相比,AIS-ZnS QD/TiO2纳米复合材料具有更好的光降解性能。TiO2浓度的增加也提高了纳米复合材料对MB的降解效率(可达99%)。MB降解动力学遵循准一阶过程。制备的AIS-ZnS QD/TiO2纳米复合材料可作为一种高效、环保的光催化剂降解MB。
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引用次数: 0
Controllable assessment of quantum rods with polarized emission for display applications 显示应用中偏振发射量子棒的可控评估
IF 2.1 4区 材料科学 Q3 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2023-01-20 DOI: 10.1088/2399-1984/acae5a
Lixuan Chen, Jinyang Zhao, Zhiqing Shi, Miao Zhou, Shenmin Zhang, Xiaowei Sun, Xin Zhang
Semiconductor quantum rods (QRs) emit polarized light, which shows great promise in the development of modern display devices with regard to energy efficiency and color enhancement. Here we demonstrate stretching of an aligned QR polarized film for brightness enhancement and optical efficiency improvement of current quantum-dot based displays. Study of the relationship between the QR material, stretching ratio and degree of alignment provides a guide for the fabrication of highly polarized QR film. A large-area film with a high degree of alignment of 0.635 and more than 1.6-fold enhancement of brightness and transmittance compared with the traditional structure was achieved, making the film a viable candidate for use in various energy-saving display devices.
半导体量子棒(QRs)发射偏振光,在现代显示设备的能效和色彩增强方面显示出巨大的前景。在这里,我们展示了对齐的QR偏振膜的拉伸,用于增强当前基于量子点的显示器的亮度和提高光学效率。研究二维码材料、拉伸比和取向度之间的关系,为高极化二维码薄膜的制备提供了指导。与传统结构相比,获得了取向度为0.635、亮度和透射率提高1.6倍以上的大面积薄膜,使该薄膜成为各种节能显示设备的可行候选者。
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引用次数: 0
Ni3S4/NiS/rGO as a promising electrocatalyst for methanol and ethanol electro-oxidation Ni3S4/NiS/rGO是一种很有前途的甲醇和乙醇电氧化电催化剂
IF 2.1 4区 材料科学 Q3 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2023-01-04 DOI: 10.1088/2399-1984/acb02b
S. Azizi, M. Askari, M. T. T. Moghadam, M. Seifi, A. Di Bartolomeo
We present a one-step hydrothermal synthesis of hybrids consisting of nickel sulfides in the form of Ni3S4–NiS (NN) and Ni3S4–NiS-rGO (NNR), i.e. with the addition of reduced graphene oxide (rGO), for application as catalysts. After accurate physical characterization and confirmation of successful synthesis, we evaluate the ability of these catalysts in the processes of methanol and ethanol oxidation. The precise electrochemical analyses show relatively good potential and excellent cyclic stability in methanol oxidation reaction (MOR) and ethanol oxidation reaction (EOR) processes. The comparison of the two catalysts shows the superiority of NNR over NN, confirming that rGO introduces a higher specific surface area and a higher electrical conductivity in the NNR structure. In the process of MOR, NNR has an oxidation peak at a current density of 55 mA cm−2 and a peak potential of 0.54 V. In EOR, this peak is located at a current density of 11 mA cm−2 and at a peak potential of 0.59 V. NNR has 97% and 94% stability in MOR and EOR after 1000 consecutive cycles, respectively, which are acceptable values.
我们提出了一步水热合成由Ni3S4-NiS (NN)和Ni3S4-NiS -rGO (NNR)形式的硫化镍组成的杂化物,即加入还原氧化石墨烯(rGO)作为催化剂。在进行了准确的物理表征和确认成功合成后,我们评估了这些催化剂在甲醇和乙醇氧化过程中的能力。精确的电化学分析表明,该材料在甲醇氧化反应(MOR)和乙醇氧化反应(EOR)过程中具有较好的应用潜力和良好的循环稳定性。两种催化剂的比较表明NNR优于NN,证实了还原氧化石墨烯在NNR结构中引入了更高的比表面积和更高的导电性。在MOR过程中,NNR在电流密度为55 mA cm−2时出现氧化峰,峰值电位为0.54 V。在EOR中,该峰值位于电流密度为11 mA cm - 2,峰值电位为0.59 V。连续1000次循环后,NNR的MOR和EOR稳定性分别为97%和94%,这是可接受的值。
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引用次数: 3
Self-assembly of bioinspired peptides for biomimetic synthesis of advanced peptide-based nanomaterials: a mini-review 仿生合成先进多肽基纳米材料的仿生多肽自组装:综述
IF 2.1 4区 材料科学 Q3 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2023-01-03 DOI: 10.1088/2399-1984/acafbe
Hao Kong, Guozheng Yang, Peng He, Danzhu Zhu, Xin Luan, Youyin Xu, RongQiu Mu, Gang Wei
The design and motif-tailoring of peptide sequences are crucial for mediating the self-assembly of peptide molecules and the biomimetic synthesis of functional peptide-based nanomaterials. It is well known that nature provides guidance and inspiration for the design and molecular tailoring of functional peptide sequences, which can further self-assemble into complex peptide nanomaterials with adjustable dimensions. In this mini-review, we summarize recent advances in the bioinspired design and regulation of functional peptide sequences by natural things, such as mussels, milk protein, silkworm silk, frogs and Alzheimer’s disease. The self-assembly of bioinspired peptides in vitro and in vivo for controlled synthesis of various peptide-based nanomaterials is introduced and analyzed. In addition, various applications of biomimetic peptide nanomaterials for biosensors, bioimaging, cancer therapy, antibacterial materials, tissue engineering, as well as energy storage and environmental science are demonstrated in detail. Finally, we give perspectives on the future development of this promising research topic. With these efforts, we hope to promote the understanding of the optimization of bioinspired peptides and the design of novel peptide nanomaterials for advanced applications.
肽序列的设计和基序剪裁对于介导肽分子的自组装和基于功能肽的纳米材料的仿生合成至关重要。众所周知,大自然为功能肽序列的设计和分子剪裁提供了指导和灵感,功能肽序列可以进一步自组装成尺寸可调的复杂肽纳米材料。在这篇小型综述中,我们总结了受生物启发设计和调节天然物质功能肽序列的最新进展,如贻贝、乳蛋白、蚕丝、青蛙和阿尔茨海默病。介绍并分析了生物启发肽在体外和体内的自组装,用于控制合成各种肽基纳米材料。此外,还详细介绍了仿生肽纳米材料在生物传感器、生物成像、癌症治疗、抗菌材料、组织工程以及储能和环境科学等方面的各种应用。最后,对本课题的发展前景进行了展望。通过这些努力,我们希望促进对生物启发肽的优化和用于高级应用的新型肽纳米材料的设计的理解。
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引用次数: 1
Amplified plasmonic emission enhancement of PbS quantum dots via Al-oxide/PMMA heterostructures Al-oxide/PMMA异质结构增强PbS量子点的放大等离子体发射
IF 2.1 4区 材料科学 Q3 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2022-12-06 DOI: 10.1088/2399-1984/aca943
S. M. Sadeghi, Rithvik R. Gutha, C. Sharp
We study the impact of Al oxide/Poly(methyl methacrylate) (PMMA) interface on plasmonic emission enhancement of infrared semiconductor quantum dots (QDs). For this, PbS QDs embedded in PMMA matrix are deposited on the top of heterostructures consisting of a Au thin film, a dielectric spacer, and an ultrathin layer of Al oxide. Our results suggest that such structures can support an emission enhancement far more than what can be reached in the cases when the QDs/PMMA films are placed on Au thin film/dielectric spacer directly, i.e. in the absence of the Al oxide. We also demonstrate that Au/Si/Al oxide/PMMA heterostructures can increase the photo-induced fluorescence enhancement of PbS QDs, making them brighter as they are irradiated with a laser field. We discuss these results in terms of combined effects of plasmonic field enhancement (Purcell effect) and the carboxylate anion bonds formed at the Al oxide/PMMA interface.
研究了氧化铝/聚甲基丙烯酸甲酯(PMMA)界面对红外半导体量子点(QDs)等离子体发射增强的影响。为此,将嵌入PMMA基体中的PbS量子点沉积在由Au薄膜、介电间隔层和超薄氧化铝层组成的异质结构的顶部。我们的研究结果表明,这种结构可以支持发射增强,远远超过直接将量子点/PMMA薄膜放置在Au薄膜/介电间隔片上的情况,即在没有氧化铝的情况下。我们还证明了Au/Si/Al氧化物/PMMA异质结构可以增加PbS量子点的光诱导荧光增强,使它们在激光场照射下更亮。我们从等离子体场增强(Purcell效应)和在氧化铝/PMMA界面形成的羧酸阴离子键的综合效应方面讨论了这些结果。
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引用次数: 1
Using nanomaterials to enhance the additive manufacturing of polymeric resins 利用纳米材料增强聚合物树脂的增材制造
IF 2.1 4区 材料科学 Q3 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2022-11-08 DOI: 10.1088/2399-1984/aca130
Ava G. Crowley, T. Tran, Micah J. Green
Additive manufacturing (AM) technologies, also called 3D printing, have dramatically developed over the past decade to allow new capabilities in materials processing with printed resolution comparable to that of traditional manufacturing techniques. Sequential layer deposition can lead to the creation of complex parts with minimized material waste, high manufacturing throughput, and increased prototyping ability, while also meeting the demand for mid- and low-volume production. The AM of polymer nanocomposites is a growing area of research because nanomaterial additives can enhance the mechanical, electrical, and other properties for end-use applications. However, the use of nanomaterial inclusions can also enhance the AM processes themselves. Here, we discuss works where nanomaterials are employed as local heaters for fused deposition modeling, as viscosifiers for direct ink writing, and as photothermal sensitizers for selective laser sintering and vat polymerization. We also note the disconnect between the researched AM capabilities and current industrial manufacturing; nanomaterials can bridge the technological gap and lead to new common practices in industrial manufacturing spaces.
增材制造(AM)技术,也称为3D打印,在过去十年中得到了巨大的发展,使材料处理的新能力与传统制造技术的打印分辨率相当。顺序层沉积可以产生复杂的零件,最大限度地减少材料浪费,提高生产吞吐量,提高原型设计能力,同时满足中、低批量生产的需求。聚合物纳米复合材料的AM是一个不断增长的研究领域,因为纳米材料添加剂可以增强最终用途的机械、电学和其他性能。然而,纳米材料夹杂物的使用也可以增强AM工艺本身。在这里,我们讨论了将纳米材料用作熔融沉积建模的局部加热器、直接墨水书写的增粘剂以及选择性激光烧结和还原聚合的光热增敏剂的工作。我们还注意到所研究的AM能力与当前工业制造之间的脱节;纳米材料可以弥合技术差距,并在工业制造领域引入新的通用做法。
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引用次数: 5
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