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Front Matter: Volume 11089 封面:第11089卷
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引用次数: 0
Designer thin-film based perfect light absorption and its applications in structural coloring, gas sensing, and solar-thermal conversion (Conference Presentation) 基于设计薄膜的完美光吸收及其在结构着色、气体传感和光热转换中的应用(会议报告)
Mohamed El Kabbash, T. Letsou, M. Hinczewski, G. Strangi, Chunlei Guo
Perfect light absorption (PLA) in nanophotonics has a wide range of applications from solar-thermal based applications to radiative cooling. However, most of the proposed platforms require intense lithography which makes them of minor practical relevance. On the other hand, thin-film light absorbers are lithographically free and can be deposited cheaply on large area based on matured technologies. However, thin-film light absorbers were thought to have major limitation and cannot be tailored compared to metamaterials. Here, we show how to design PLA using thin-films in terms of wavelength range, bandwidth, spatial profile of optical losses, directionality and iridescence. We also show that iridescent free, PLA can occur by simply heating metallic thin-films when the metal is of low reflectance and its oxide is of high refractive index. We theoretically and experimentally demonstrate Generalized Brewster angle effect in thin film light absorbers. In addition, we demonstrate hydrogen sensing using three different PLA strategies showing record sensitivity and figure of merit. Furthermore, we show various strategies to create ultra-pure structural colors. Finally, we demonstrate different solar-thermal applications for novel thin-film PLA designs.
完美光吸收(PLA)在纳米光子学中有着广泛的应用,从基于太阳热的应用到辐射冷却。然而,大多数提出的平台都需要高度光刻,这使得它们的实际意义不大。另一方面,基于成熟的技术,薄膜光吸收剂无需光刻,可以廉价地大面积沉积。然而,薄膜光吸收剂被认为有很大的局限性,无法与超材料相比进行定制。在这里,我们展示了如何使用薄膜在波长范围、带宽、光学损耗的空间分布、方向性和虹彩方面设计PLA。我们还表明,当金属具有低反射率和高折射率的氧化物时,通过简单加热金属薄膜可以产生无虹彩的PLA。从理论上和实验上论证了薄膜光吸收体中的广义布鲁斯特角效应。此外,我们使用三种不同的PLA策略演示了氢传感,显示了创纪录的灵敏度和优异值。此外,我们展示了各种策略来创造超纯的结构颜色。最后,我们展示了新型薄膜PLA设计的不同太阳能热应用。
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引用次数: 0
Flexible piezoelectric nanogenerator based on sonochemically synthesized ZnO nanoflakes for self‐powered devices and wearable energy harvesting (Conference Presentation) 基于声化学合成ZnO纳米片的柔性压电纳米发电机用于自供电器件和可穿戴能量收集(会议报告)
F. Alam, S. Aghaei, A. Jalal, N. Pala
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引用次数: 1
Colorimetric humidity sensors with sub-50ms response times using randomly arranged titania microspheres (Conference Presentation) 使用随机排列的二氧化钛微球的响应时间低于50ms的比色湿度传感器(会议报告)
Syazwani Mohd Noor, Hansol Jang, Kyungnae Baek, Yi-Rong Pei, Al-Mahmnur Alam, J. Choy, J. Hyun
Disordered photonic systems as observed in iridescent insects and flowers introduces new pathways for realizing cost-effective and scalable structural colors. In this work, we present a fast-colorimetric humidity sensor derived from a disordered arrangement of polydisperse nanoporous titania microspheres. The sensor relies on changes in the total scattering of the microspheres upon variations in the surrounding humidity. The incoherent scattering from each particle allows the sum of the individual cross sections to determine the total scattering cross section, which converts the individual noisy spectra to a smoothly varying spectrum that gives rise to a saturated color.[1] We show that because the titania microspheres is highly porous with 1~2 nm-sized nanopores, water can diffuse into the particle interior via intracrystalline dynamics, thereby changing the effective permittivity and consequently the scattered color at ultra-fast speeds (sub 50ms). Our results provide a practical route toward achieving cheap, simple, scalable, ultrafast colorimetric humidity sensors using structural colors from disordered nanoporous microspheres [2]. [1] Alam, A-M; Baek K; Son J; Pei Y-R; Kim D-H; Choy J-H; and Hyun J-K. Generating Color from Polydisperse, Near Micron-Sized TiO2 Particles, ACS Appl. Mater. Interfaces, 2017, 9 (28), 23941– 23948[2] M-Noor, S; Jang, H ; Baek K; Pei Y-R; Alam, A-M; Kim,Y.H; Kim, I.S; Choy, J.H and Hyun J-K. Ultrafast humidity-responsive structural colors from disordered nanoporous titania microspheres. Submitted (2019)
在虹彩昆虫和花朵中观察到的无序光子系统为实现具有成本效益和可扩展的结构颜色引入了新的途径。在这项工作中,我们提出了一种快速比色湿度传感器,源自多分散纳米多孔二氧化钛微球的无序排列。传感器依靠微球的总散射随周围湿度的变化而变化。来自每个粒子的非相干散射允许单个横截面的总和来确定总散射横截面,这将单个噪声光谱转换为平滑变化的光谱,从而产生饱和颜色。[1]我们发现,由于二氧化钛微球具有1~2 nm大小的纳米孔,水可以通过晶内动力学扩散到颗粒内部,从而改变有效介电常数,从而以超快的速度(低于50ms)散射颜色。我们的研究结果为实现廉价、简单、可扩展、超快速的比色湿度传感器提供了一条实用的途径,该传感器使用无序纳米孔微球的结构色[2]。[1]张志强,张志强;门敏K;儿子J;裴y r;金正日d - h;白菜陶宏根;玄君坤。从多分散的近微米大小的TiO2颗粒中产生颜色,ACS应用。板牙。接口,2017,9 (28),23941 - 23948[2]张,H;门敏K;裴y r;阿拉姆,a - m;金,,12;金,即;蔡俊辉和玄俊奎。无序纳米多孔二氧化钛微球的超快速湿度响应结构色。提交(2019)
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引用次数: 0
Fabrication and characterizations of MoS2 layers on Au nanogratings (Conference Presentation) 金纳米光栅上二硫化钼层的制备与表征(会议报告)
Soyeong Kwon, M. Kwon, Jungeun Song, Eunah Kim, B. Kim, Sangwook Lee, Dong-Wook Kim
The coupling between surface plasmons (SPs) and excitons in 2D transition metal dichalcogenide (TMD) materials has been attracted growing research attention in recent days. Strong electric field confinement and absorption enhancement could be expected, as a result of the SP-excition couping. We prepared exfoliated flakes of MoS2, a representative TMD material, on Au nanogratings fabricated by electron beam lithography. We studied influences of propagating SP on optical properties of the MoS2 flakes on the Au nanogratings, based on both experimental measurements and numerical calculations. Local surface potential maps of the samples suggested that the strain states in the MoS2 flakes and the dipoles formed at the MoS2/ Au interface could cause spatial modulation of the bandgap energies of the MoS2 flakes. The surface potential measurements were carried out using Kelvin probe force microscopy in dark and under TM/TE-mode light illumination. Band diagrams of the MoS2/Au nanogratings were proposed to explain all the experimental results. This study can help us to understand and control the physical characteristics of the TMD/metal nanostructures.
二维过渡金属二硫化物(TMD)材料中表面等离子体激子与激子之间的耦合是近年来研究的热点。由于sp -激振耦合,可以预期强电场约束和吸收增强。利用电子束光刻技术在金纳米光栅上制备了具有代表性的TMD材料二硫化钼的剥离薄片。在实验测量和数值计算的基础上,研究了SP对MoS2薄片在金纳米光栅上光学性能的影响。样品的局部表面电位图表明,MoS2薄片中的应变状态和MoS2/ Au界面上形成的偶极子可以引起MoS2薄片带隙能量的空间调制。使用开尔文探针力显微镜在黑暗和TM/ te模式光照下测量表面电位。提出了MoS2/Au纳米光栅的能带图来解释所有的实验结果。该研究有助于我们理解和控制TMD/金属纳米结构的物理特性。
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引用次数: 0
Next-generation materials for hybrid electro-optic systems (Conference Presentation) 用于混合电光系统的新一代材料(会议报告)
L. Johnson, Huajun Xu, Y. D. Coene, D. Elder, K. Clays, L. Dalton, B. Robinson
Recent developments in hybrid electro-optic (EO) systems, in which an organic material with an ultra-large second-order susceptibility is combined with silicon (SOH) or gold (POH) waveguides at the nanoscale. Tight confinement of the optical and RF fields in such devices has enabled operating frequencies > 300 GHz and voltage-length parameters (UπL) < 40 V-μm with existing high-performance organic electro-optic (OEO) materials. However, achieving UπL values on the order of 1 V-μm will require a new generation of OEO materials. The short path lengths within hybrid devices greatly alleviate concerns about optical loss, enabling development of OEO chromophores with extraordinarily large hyperpolarizabilities and refractive indices at telecom wavelengths. However, as device dimensions shrink, chromophore-surface interactions, space-efficiency, and refractive index anisotropy become more critical. Practical device implementations also require materials with high thermal and chemical stability and uncompromising EO performance. We have used a theory-aided design process applying classical and quantum mechanical techniques to design a new generation of OEO materials intended to meet the needs of hybrid devices. We have synthesized these materials, characterized their hyperpolarizability by hyper-Rayleigh scattering, and evaluated their bulk electro-optic behavior and prospects for implementation in nanoscale devices.
混合电光(EO)系统的最新进展,其中具有超大二阶磁化率的有机材料在纳米尺度上与硅(SOH)或金(POH)波导结合。现有的高性能有机电光(OEO)材料对光学和射频场的严格限制使得工作频率> 300 GHz,电压长度参数(UπL) < 40 V-μm成为可能。然而,要达到1 V-μm量级的UπL值,需要新一代的OEO材料。混合器件内的短路径长度大大减轻了对光学损耗的担忧,从而使在电信波长下具有超大超极化率和折射率的OEO发色团得以开发。然而,随着器件尺寸的缩小,发色团-表面相互作用、空间效率和折射率各向异性变得更加关键。实际设备的实现还需要具有高热稳定性和化学稳定性以及不妥协的EO性能的材料。我们使用理论辅助设计过程,应用经典和量子力学技术来设计新一代OEO材料,旨在满足混合设备的需求。我们已经合成了这些材料,通过超瑞利散射表征了它们的超极化性,并评估了它们的体电光行为和在纳米级器件中的应用前景。
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引用次数: 3
Thin nanostructured perovskite films for high performance photo-electronic applications (Conference Presentation) 高性能光电应用的纳米钙钛矿薄膜(会议报告)
Cheolmin Park
Ordered nanostructured crystals of thin perovskites films are of great interest to researchers because of the dimensional-dependence of their photoelectronic properties for developing the perovskites with novel properties. In this presentation, both top-down and bottom-up approaches for fabricating nanostructured perovskite films are demonstrated. First, a variety of micro/nanopatterns of a perovskite film are fabricated by either microimprinting or transfer-printing a thin spin-coated precursor film in soft-gel state with a topographically pre-patterned polymer mold, followed by thermal treatment for complete conversion of the precursor film to a perovskite one. Second, we also demonstrate a simple and robust route, involving the controlled crystallization of the perovskites templated with a self-assembled block copolymer (BCP), for fabricating nanopatterned perovskite films with various shapes and nanodomain sizes. When the precursor ion solution of a perovskite and poly(styrene)-block-poly(2-vinylpyridine) (PS-b-P2VP) was spin-coated on the substrate, a nanostructured BCP was developed by microphase separation. Spontaneous crystallization of the precursor ions preferentially coordinated with the P2VP domains yielded ordered nanocrystals with various nanostructures. The nanopatterned perovskites showed significantly enhanced photoluminescence (PL) with high resistance to both humidity and heat due to geometrically confining crystals in and passivation with the P2VP chains. The self-assembled perovskite films with high PL performance provided a facile control of color coordinates by color conversion layers in blue-emitting devices for cool-white emission.
钙钛矿薄膜的有序纳米结构晶体是研究人员非常感兴趣的,因为它们的光电子性质的尺寸依赖于开发具有新性质的钙钛矿。在本报告中,演示了自顶向下和自底向上制备纳米结构钙钛矿薄膜的方法。首先,通过微压印或转移印刷,用地形预图案聚合物模具将一层薄的自旋涂层前驱体膜制成软凝胶状态,然后通过热处理将前驱体膜完全转化为钙钛矿膜,从而制备出钙钛矿膜的各种微/纳米图案。其次,我们还展示了一种简单而可靠的方法,包括用自组装嵌段共聚物(BCP)模板化钙钛矿的控制结晶,用于制造具有各种形状和纳米畴尺寸的纳米图案钙钛矿薄膜。将钙钛矿-聚苯乙烯-嵌段-聚(2-乙烯基吡啶)(PS-b-P2VP)前驱体离子溶液自旋涂覆在衬底上,通过微相分离制备了纳米结构的BCP。前驱体离子与P2VP结构域优先配位的自发结晶产生了具有不同纳米结构的有序纳米晶体。由于晶体在P2VP链上的几何限制和P2VP链的钝化作用,纳米钙钛矿的光致发光(PL)性能显著增强,具有较高的耐湿热性能。具有高PL性能的自组装钙钛矿薄膜为冷白发射蓝光器件中的颜色转换层提供了方便的颜色坐标控制。
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引用次数: 0
Two-dimensional MoS2-enabled flexible rectenna for wireless energy harvesting in the Wi-Fi band (Conference Presentation) 用于Wi-Fi频段无线能量收集的二维mos2柔性整流天线(会议报告)
Xu Zhang, J. Grajal, J. Vazquez-Roy, U. Radhakrishna, Xiaoxue Wang, W. Chern, Lin Zhou, Yuhao Zhang, Han Wang, M. Dubey, J. Kong, M. Dresselhaus, T. Palacios
MoS2 has attracted substantial attention due to its atomic thickness and outstanding electronic and mechanical properties. As one of the thinnest semiconductors in the world, MoS2 is promising to build flexible electronics that can be integrated with objects with arbitrary shapes and inspires a vision of distributed ubiquitous electronics. Despite recent advances in two-dimensional materials-based electronics (e.g. 2D materials-based transistors, memory devices and sensors), an efficient and flexible energy harvesting solution is necessary, but still missing, to enable a self-powered system. At the same time, the electromagnetic (EM) radiation in the Wi-Fi band (2.4 GHz and 5.9 GHz) is becoming increasingly ubiquitous and it would be beneficial to be able to wirelessly harvest it to power future distributed electronics. However, the rectennas (i.e. RF energy harvesters) based on flexible semiconductors have not been fast enough to cover the Wi-Fi band due to their limited transport properties. Here we present a unique MoS2 semiconducting-metallic phase heterojunction, which enables a flexible and high-speed Schottky diode with a cutoff frequency of 10 GHz. Due to a novel lateral architecture and self-aligned phase engineering, our MoS2 Schottky diode exhibits significantly reduced parasitic capacitance and series resistance. By integrating the MoS2 rectifier with a flexible Wi-Fi band antenna, we successfully fabricate a fully flexible rectenna that demonstrates direct energy harvesting of EM radiation in the Wi-Fi band with zero external bias (battery-free). Moreover, taking advantage of the nonlinearity of the MoS2 Schottky diode, a frequency mixing in the gigahertz range is also successfully demonstrated on flexible substrates.
二硫化钼由于其原子厚度和优异的电子力学性能而引起了人们的广泛关注。作为世界上最薄的半导体之一,MoS2有望构建灵活的电子产品,可以与任意形状的物体集成,并激发分布式无处不在的电子产品的愿景。尽管基于二维材料的电子器件(例如基于二维材料的晶体管、存储器件和传感器)最近取得了进展,但要实现自供电系统,高效灵活的能量收集解决方案是必要的,但仍然缺乏。与此同时,Wi-Fi频段(2.4 GHz和5.9 GHz)的电磁(EM)辐射正变得越来越普遍,能够无线收集电磁辐射为未来的分布式电子设备供电将是有益的。然而,基于柔性半导体的整流天线(即射频能量收集器)由于其有限的传输特性,速度不够快,无法覆盖Wi-Fi频段。在这里,我们提出了一种独特的MoS2半导体-金属相异质结,它可以实现截止频率为10 GHz的柔性高速肖特基二极管。由于新的横向结构和自对准相位工程,我们的MoS2肖特基二极管具有显着降低的寄生电容和串联电阻。通过将MoS2整流器与灵活的Wi-Fi频段天线集成,我们成功地制造了一个完全灵活的整流天线,该整流天线展示了在Wi-Fi频段零外部偏置(无电池)下电磁辐射的直接能量收集。此外,利用MoS2肖特基二极管的非线性特性,在柔性衬底上成功地实现了千兆赫范围内的频率混合。
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引用次数: 2
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Nanoengineering: Fabrication, Properties, Optics, Thin Films, and Devices XVI
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