Scanning probe microscopy

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Laser scan of the scanning photocurrent microscope

Scanning Probe Microscopy (SPM) is a branch of microscopy that forms images of surfaces using a physical probe that scans the specimen. SPM was developed in the 1980s, with the invention of the Atomic Force Microscope (AFM) and the Scanning Tunneling Microscope (STM), which revolutionized the field of nanotechnology and surface science by providing atomic and near-atomic resolution images of materials. Unlike traditional forms of microscopy, such as optical microscopy and electron microscopy, SPM techniques do not use lenses or beams of electrons or photons to create images. Instead, they rely on the physical interaction between a probe and the surface of the material being studied.

Overview[edit | edit source]

The basic principle behind SPM involves the use of a sharp probe that is brought very close to the surface of a specimen. As the probe scans across the surface, various interactions between the probe and the surface can be measured, and these measurements are used to generate images of the surface at high resolution. The nature of the interaction depends on the specific type of SPM being used. For example, in STM, the interaction is based on quantum tunneling of electrons between the probe and the surface, while in AFM, the interaction can be based on van der Waals forces, mechanical contact force, or other forces.

Types of Scanning Probe Microscopy[edit | edit source]

There are several types of SPM, each based on different types of interactions between the probe and the specimen:

  • Scanning Tunneling Microscope (STM): Utilizes quantum tunneling of electrons between a sharp probe and the surface to generate images at atomic resolution.
  • Atomic Force Microscope (AFM): Measures the forces between the probe and the surface to image the topography and properties of the surface at nanometer to atomic resolution.
  • Magnetic Force Microscopy (MFM): A variation of AFM that measures variations in magnetic forces on the surface.
  • Near-field Scanning Optical Microscopy (NSOM or SNOM): Uses the interaction of light with the surface at a very short distance to overcome the diffraction limit of light and achieve higher resolution.

Applications[edit | edit source]

SPM techniques have a wide range of applications in various fields such as physics, chemistry, biology, and materials science. They are used for imaging surfaces at atomic to nanometer resolution, measuring surface roughness, studying surface reactions, and characterizing physical, chemical, and mechanical properties of materials at the nanoscale.

  • In materials science, SPM is used to study the properties of polymers, metals, semiconductors, and thin films.
  • In biology, AFM, in particular, is used to image cells, membranes, proteins, and DNA, providing insights into biological processes at the molecular level.
  • In chemistry, SPM techniques are used to observe chemical reactions on surfaces and to study catalysis.

Advantages and Limitations[edit | edit source]

The main advantage of SPM is its ability to image surfaces at atomic or near-atomic resolution without the need for vacuum conditions, unlike electron microscopy. SPM techniques can also be used in various environments, including air, vacuum, and liquid, making them versatile tools for studying a wide range of materials and biological specimens.

However, SPM also has limitations. The requirement for a physical probe can lead to sample damage, especially for soft or fragile materials. The scanning process can be slow, and the interpretation of SPM data can be complex, requiring sophisticated software and expertise.

Conclusion[edit | edit source]

Scanning Probe Microscopy represents a significant advancement in the field of microscopy, offering unparalleled resolution and versatility in imaging surfaces and studying material properties at the nanoscale. As technology continues to evolve, SPM techniques are expected to find even broader applications, furthering our understanding of the nanoworld.

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Contributors: Prab R. Tumpati, MD