Near-field scanning optical microscopy (NSOM) or scanning near-field optical microscopy (SNOM) is a microscopy technique for nanostructure investigation that breaks the far field resolution limit by exploiting the properties of evanescent waves. In SNOM, the excitation laser light is focused through an aperture with a diameter smaller than the excitation wavelength, resulting in an evanescent field (or near-field) on the far side of the aperture. When the sample is scanned at a small distance below the aperture, the optical resolution of transmitted or reflected light is limited only by the diameter of the aperture. In particular, lateral resolution of 6 nm and vertical resolution of 2–5 nm have been demonstrated. As in optical microscopy, the contrast mechanism can be easily adapted to study different properties, such as refractive index, chemical structure and local stress. Dynamic properties can also be studied at a sub-wavelength scale using this technique. NSOM/SNOM is a form of scanning probe microscopy.
History Edward Hutchinson Synge is given credit for conceiving and developing the idea for an imaging instrument that would image by exciting and collecting diffraction in the near field. His original idea, proposed in 1928, was based upon the usage of intense nearly planar light from an arc under pressure behind a thin, opaque metal film with a small orifice of about 100 nm. The orifice was to remain within 100 nm of the surface, and information was to be collected by point-by-point scanning. He foresaw the illumination and the detector movement being the biggest technical difficulties. John A. O'Keefe also developed similar theories in 1956. He thought the moving of the pinhole or the detector when it is so close to the sample would be the most likely issue that could prevent the realization of such an instrument. It was Ash and Nicholls at University College London who, in 1972, first broke the Abbe's diffraction limit using microwave radiation with a wavelength of 3 cm. A line grating was resolved with a resolution of λ0/60. A decade later, a patent on an optical near-field microscope was filed by Dieter Pohl, followed in 1984 by the first paper that used visible radiation for near field scanning. The near-field optical (NFO) microscope involved a sub-wavelength aperture at the apex of a metal coated sharply pointed transparent tip, and a feedback mechanism to maintain a constant distance of a few nanometers between the sample and the probe. Lewis et al. were also aware of the potential of an NFO microscope at this time. They reported first results in 1986 confirming super-resolution. In both experiments, details below 50 nm (about λ0/10) in size could be recognized.
Theory According to Abbe's theory of image formation, developed in 1873, the resolving capability of an optical component is ultimately limited by the spreading out of each image point due to diffraction. Unless the aperture of the optical component is large enough to collect all the diffracted light, the finer aspects of the image will not correspond exactly to the object. The minimum resolution (d) for the optical component is thus limited by its aperture size, and expressed by the Rayleigh criterion:
d = 0.61 λ 0 N A {\displaystyle d=0.61{\frac {\lambda _{0}}{N\!A}}\;\!}
Here, λ0 is the wavelength in vacuum; NA is the numerical aperture for the optical component (maximum 1.3–1.4 for modern objectives with a very high magnification factor). Thus, the resolution limit is usually around λ0/2 for conventional optical microscopy. This treatment takes into account only the light diffracted into the far-field that propagates without any restrictions. NSOM makes use of evanescent or non propagating fields that exist only near the surface of the object. These fields carry the high frequency spatial information about the object and have intensities that drop off exponentially with distance from the object. Because of this, the detector must be placed very close to the sample in the near field zone, typically a few nanometers. As a result, near field microscopy remains primarily a surface inspection technique. The detector is then rastered across the sample using a piezoelectric stage. The scanning can either be done at a constant height or with regulated height by using a feedback mechanism.
Modes of operation
Aperture and apertureless operation
There exist NSOM which can be operated in so-called aperture mode and NSOM for operation in a non-aperture mode. As illustrated, the tips used in the apertureless mode are very sharp and do not have a metal coating.
Though there are many issues associated with the apertured tips (heating, artifacts, contrast, sensitivity, topology and interference among others), aperture mode remains more popular. This is primarily because apertureless mode is even more complex to set up and operate, and is not understood as well. There are five primary modes of apertured NSOM operation and four primary modes of apertureless NSOM operation. The major ones are illustrated in the next figure.
Some types of NSOM operation utilize a campanile probe, which has a square pyramid shape with two facets coated with a metal. Such a probe has a high signal collection efficiency (>90%) and no frequency cutoff. Another alternative is "active tip" schemes, where the tip is functionalized with active light sources such as a fluorescent dye or even a light emitting diode that enables fluorescence excitation. The merits of aperture and apertureless NSOM configurations can be merged in a hybrid probe design, which contains a metallic tip attached to the side of a tapered optical fiber. At visible range (400 nm to 900 nm), about 50% of the incident light can be focused to the tip apex, which is around 5 nm in radius. This hybrid probe can deliver the excitation light through the fiber to realize tip-enhanced Raman spectroscopy (TERS) at tip apex, and collect the Raman signals through the same fiber. The lens-free fiber-in-fiber-out STM-NSOM-TERS has been demonstrated.
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![Near-field scanning optical microscope: Diagram illustrating near-field optics, with the diffraction of light coming from NSOM fiber probe, showing wavelength of light and the near-field.[1]](https://upload.wikimedia.org/wikipedia/commons/thumb/d/d1/Nearfield_optics.png/330px-Nearfield_optics.png?utm_source=en.wikipedia.org&utm_campaign=parser&utm_content=thumbnail)
![Near-field scanning optical microscope: Comparison of photoluminescence maps recorded from a molybdenum disulfide flake using NSOM with a campanile probe (top) and conventional confocal microscopy (bottom). Scale bars: 1 μm.[2]](https://upload.wikimedia.org/wikipedia/commons/thumb/e/e1/Campanile_probe_vs_confocal_PL_maps.jpg/330px-Campanile_probe_vs_confocal_PL_maps.jpg?utm_source=en.wikipedia.org&utm_campaign=parser&utm_content=thumbnail)
![Near-field scanning optical microscope: Sketch of a) typical metal-coated tip, and b) sharp uncoated tip.[19]](https://upload.wikimedia.org/wikipedia/commons/thumb/5/5e/NSOM-tips.png/500px-NSOM-tips.png?utm_source=en.wikipedia.org&utm_campaign=parser&utm_content=thumbnail)
![Near-field scanning optical microscope: Apertured modes of operation: a) illumination, b) collection, c) illumination collection, d) reflection and e) reflection collection.[20]](https://upload.wikimedia.org/wikipedia/commons/thumb/e/eb/NSOM-apertured.png/1280px-NSOM-apertured.png?utm_source=en.wikipedia.org&utm_campaign=parser&utm_content=thumbnail)
![Near-field scanning optical microscope: Apertureless modes of operation: a) photon tunneling (PSTM) by a sharp transparent tip, b) PSTM by sharp opaque tip on smooth surface, and c) scanning interferometric apertureless microscopy with double modulation.[19]](https://upload.wikimedia.org/wikipedia/commons/thumb/c/ca/NSOM-apertureless.png/500px-NSOM-apertureless.png?utm_source=en.wikipedia.org&utm_campaign=parser&utm_content=thumbnail)
