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红外对抗系统与技术经历了近半个多世纪的发展,先后出现了红外干扰机、红外诱饵及红外烟幕等几类红外干扰技术,并形成了一个庞大的红外干扰器材家族.近年来,随着红外成像寻的制导武器和技术的发展,常规的红外干扰手段对新型红外制导武器的干扰效果越来越不尽人意,人们逐渐提出了以高功率氙灯或激光作为红外能量源的定向红外对抗(DIRCM)概念.该系统具备优越的红外干扰性能,如通过干扰、致眩和毁伤等干扰红外成像导引头、多次重复使用、干扰效率高等,现已成为新一代红外对抗系统的优选方案.回顾了近年来国外新一代定向红外对抗系统和技术的研究发展历程,重点阐述了基于激光的定向红外对抗系统的工作原理、干扰毁伤机理、在技术上的优势及其国外发展现状,预测了定向红外对抗系统与技术的发展趋势. 相似文献
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Widely Tunable Morphologies in Block Copolymer Thin Films Through Solvent Vapor Annealing Using Mixtures of Selective Solvents
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Michelle A. Chavis Detlef‐M. Smilgies Ulrich B. Wiesner Christopher K. Ober 《Advanced functional materials》2015,25(20):3057-3065
Thin films of block copolymers are extremely attractive for nanofabrication because of their ability to form uniform and periodic nanoscale structures by microphase separation. One shortcoming of this approach is that to date the design of a desired equilibrium structure requires synthesis of a block copolymer de novo within the corresponding volume ratio of the blocks. In this work, solvent vapor annealing in supported thin films of poly(2‐hydroxyethyl methacrylate)‐block‐poly(methyl methacrylate) [PHEMA‐b‐PMMA] by means of grazing incidence small angle X‐ray scattering (GISAXS) is investigated. A spin‐coated thin film of a lamellar block copolymer is solvent vapor annealed to induce microphase separation and improve the long‐range order of the self‐assembled pattern. Annealing in a mixture of solvent vapors using a controlled volume ratio of solvents, which are chosen to be preferential for each block, enables selective formation of ordered lamellae, gyroid, hexagonal, or spherical morphologies from a single‐block copolymer with a fixed volume fraction. The selected microstructure is then kinetically trapped in the dry film by rapid drying. This paper describes what is thought to be the first reported case where in situ methods are used to study the transition of block copolymer films from one initial disordered morphology to four different ordered morphologies, covering much of the theoretical diblock copolymer phase diagram. 相似文献
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Efficiently Releasing the Trapped Energy Flow in White Organic Light‐Emitting Diodes with Multifunctional Nanofunnel Arrays
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Lei Zhou Qing‐Dong Ou Yan‐Qing Li Heng‐Yang Xiang Lu‐Hai Xu Jing‐De Chen Chi Li Su Shen Shuit‐Tong Lee Jian‐Xin Tang 《Advanced functional materials》2015,25(18):2660-2668
White organic light‐emitting diodes (OLEDs) hold great promise for applications in displays and lighting due to high efficiency and superior white color balance. However, further improvement in efficiency remains a continuous and urgent demand due to limited energy flow extraction. A powerful method for drastically releasing the trapped energy flow in conventional white OLEDs is demonstrated by implementing unique quasi‐periodic subwavelength nanofunnel arrays (NFAs) via soft nanoimprinting lithography, which is ideal for enhancing light extraction without any spectral distortion or angular dependence. The resulting efficiency is over 2 times that of a conventional OLED used as a comparison. The external quantum efficiency and power efficiency are raised to 32.4% and 56.9 lm W?1, respectively. Besides, the substantial increase in efficiency over a broad bandwidth with angular color stability, the experimental proofs show that the NFA‐based extraction structure affords the enticing capacity against scrubbing and the self‐cleaning feature, which are critical to the commercial viability in practical applications. 相似文献
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Tarek Abu‐Husein Swen Schuster Martin Kind Tobias Santowski Adrian Wiesner Ryan Chiechi Egbert Zojer Andreas Terfort Michael Zharnikov 《Advanced functional materials》2015,25(25):3943-3957
Using a representative model system, here electronic and structural properties of aromatic self‐assembled monolayers (SAMs) are described that contain an embedded, dipolar group. As polar unit, pyrimidine is used, with its orientation in the molecular backbone and, consequently, the direction of the embedded dipole moment being varied. The electronic and structural properties of these embedded‐dipole SAMs are thoroughly analyzed using a number of complementary characterization techniques combined with quantum‐mechanical modeling. It is shown that such mid‐chain‐substituted monolayers are highly interesting from both fundamental and application viewpoints, as the dipolar groups are found to induce a potential discontinuity inside the monolayer, electrostatically shifting the core‐level energies in the regions above and below the dipoles relative to one another. These SAMs also allow for tuning the substrate work function in a controlled manner independent of the docking chemistry and, most importantly, without modifying the SAM‐ambient interface. 相似文献
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