2007
DOI: 10.1109/jstqe.2007.910799
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Differential Near-Field Scanning Optical Microscopy Using Sensor Arrays

Abstract: Abstract-In this paper, we introduce a new aperture-type nearfield scanning optical microscopy (NSOM) imaging concept that relies on specially designed large-area (e.g., >200 nm × 200 nm) aperture geometries having sharp corners. Unlike in conventional NSOM, the spatial resolution of this near-field imaging modality is not determined by the size of the aperture, but rather by the sharpness of the corners of the large aperture. This approach significantly improves the light throughput of the near-field probe an… Show more

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Cited by 9 publications
(5 citation statements)
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“…6 Hence the current gold standard for nanoimaging remains electron microscopy in both transmission (TEM) and scanning (SEM) modes, despite the required large capital investment, extensive sample preparation, and incompatibility with live-cell imaging. Scanning probe microscopy techniques [7][8][9][10][11][12] may also be used, although they still require a large capital investment, involve long acquisition times, and are in general incompatible with live-cell imaging. To provide new solutions for high-resolution imaging needs, the last decade has seen the invention of several super-resolution optical techniques, including structured illumination micro-scopy, [13][14][15] photoactivated localization microscopy (PALM), 16 stochastic optical reconstruction microscopy (STORM), 17 and stimulated emission depletion microscopy (STED).…”
Section: Introductionmentioning
confidence: 99%
“…6 Hence the current gold standard for nanoimaging remains electron microscopy in both transmission (TEM) and scanning (SEM) modes, despite the required large capital investment, extensive sample preparation, and incompatibility with live-cell imaging. Scanning probe microscopy techniques [7][8][9][10][11][12] may also be used, although they still require a large capital investment, involve long acquisition times, and are in general incompatible with live-cell imaging. To provide new solutions for high-resolution imaging needs, the last decade has seen the invention of several super-resolution optical techniques, including structured illumination micro-scopy, [13][14][15] photoactivated localization microscopy (PALM), 16 stochastic optical reconstruction microscopy (STORM), 17 and stimulated emission depletion microscopy (STED).…”
Section: Introductionmentioning
confidence: 99%
“…For relative amplitudes equal to 0.1% the observed added noise in the simulation results does not exceed 20% of the surface amplitude. The method can be implemented using a high performance piezoelectric stage, similar equipment is used for scanning tip displacement in NSOM and aperture displacement in DNSOM as used in [1,2,3,4,5,7]. Variations of the signal due to the 20nm by 20nm square roughness of the surface profile are predicted to be about ~ 1% , therefore tolerated noise for this system cannot exceed ~0.01% for optimal surface detection.…”
Section: Efsom With Enhancement By Surface Plasmons Polaritonsmentioning
confidence: 99%
“…The vertical resolution of the EFSOM depends on the strength of evanescentfields, vertical displacement of the sample and the dynamic range of the photo-detector, while lateral resolution depends on the evanescent-field decay and scanning velocity. Image reconstruction is achieved by taking the spatial derivative of the recorded map similar to [6,7].…”
Section: Introductionmentioning
confidence: 99%
“…Another early method of nano-imaging is the near-field scanning optical microscope (NSOM or SNOM) [1518]. This device is practically similar to an atomic force microscope (AFM) in that a sharp probe tip is mechanically scanned across a surface while maintaining contact (or a very small gap of < 100 nm) with the surface.…”
Section: Introductionmentioning
confidence: 99%