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Optical Detection and Sizing of Single Nano-Particles Using Continuous Wetting Films

机译:使用连续润湿膜对单个纳米颗粒进行光学检测和定尺寸

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摘要

The physical interaction between nano-scale objects and liquid interfaces can create unique optical properties, enhancing the signatures of the objects with sub-wavelength features. Here we show that the evaporation on a wetting substrate of a polymer solution containing sub-micrometer or nano-scale particles creates liquid micro-lenses that arise from the local deformations of the continuous wetting film. These micro-lenses have properties similar to axicon lenses that are known to create beams with a long depth of focus. This enhanced depth of focus allows detection of single nanoparticles using a low magnification microscope objective lens, achieving a relatively wide field-of-view, while also lifting the constraints on precise focusing onto the object plane. Hence, by creating these liquid axicon lenses through spatial deformations of a continuous thin wetting film, we transfer the challenge of imaging individual nano-particles to detecting the light focused by these lenses. As a proof of concept, we demonstrate the detection and sizing of single nano-particles (100 and 200 nm), CpGV granuloviruses as well as Staphylococcus epidermidis bacteria over a wide field of view of e.g., 5.10×3.75 mm2 using a ×5 objective lens with a numerical aperture of 0.15. In addition to conventional lens-based microscopy, this continuous wetting film based approach is also applicable to lensfree computational on-chip imaging, which can be used to detect single nano-particles over a large field-of-view of e.g., >20-30 mm2. These results could be especially useful for high-throughput field-analysis of nano-scale objects using compact and cost-effective microscope designs.
机译:纳米级物体和液体界面之间的物理相互作用可以创建独特的光学特性,从而增强具有亚波长特征的物体的特征。在这里,我们表明,包含亚微米或纳米级颗粒的聚合物溶液在润湿基材上的蒸发会产生由连续润湿膜的局部变形引起的液体微透镜。这些微透镜具有类似于轴锥透镜的特性,已知该轴锥透镜会产生具有长焦深的光束。这种增强的聚焦深度允许使用低倍率显微镜物镜检测单个纳米颗粒,从而获得相对宽的视野,同时也消除了将精确聚焦到物平面上的限制。因此,通过通过连续的湿润薄膜的空间变形来创建这些液体轴锥透镜,我们将对单个纳米粒子成像的挑战转移到了检测这些透镜聚焦的光上。作为概念的证明,我们证明了在例如5.10×3.75 mm 2 <的宽视场中对单个纳米粒子(100和200 nm),CpGV颗粒病毒以及表皮葡萄球菌的检测和大小确定。 / sup>使用数值孔径为0.15的×5物镜。除了传统的基于透镜的显微镜之外,这种基于连续湿膜的方法还适用于无透镜计算的芯片上成像,该成像可用于在大于20的大视场中检测单个纳米粒子。 30毫米 2 。这些结果对于使用紧凑且具有成本效益的显微镜设计对纳米级物体进行高通量现场分析特别有用。

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