Introduction:
SEM stands for Scanning Electron Microscopy, which is a type of electron microscopy used to obtain high-resolution images of materials and biological specimens at the nanoscale.
The basic working principle of SEM involves the use of a beam of
high-energy electrons that are focused onto a sample using electromagnetic
lenses. The electrons interact with the sample, causing the emission of
secondary electrons and backscattered electrons, which are detected and used to
generate an image of the surface of the sample. SEM images can provide
high-resolution details about surface topography, morphology, and elemental
composition. Its function of it is in Figure 1.
Figure 1: SEM working arrangement. |
One of the major applications of SEM is in materials science, where it is used to study the microstructure of materials and to characterize their properties. SEM is also widely used in the biological sciences to study the structure and function of cells and tissues.
The acceleration voltage is an important parameter in SEM, as it
affects the interaction between the electron beam and the sample. Increasing
the acceleration voltage can result in higher-resolution images, as
higher-energy electrons can penetrate deeper into the sample and generate more
secondary and backscattered electrons. However, higher acceleration voltages
can also cause damage to the sample and may affect the results of the imaging.
The choice of acceleration voltage, therefore, depends on the nature of the
sample and the specific application.
In addition to imaging, SEM can also be used for various other
analytical techniques, such as energy-dispersive X-ray spectroscopy (EDS) and
electron backscatter diffraction (EBSD), which can provide information about
the elemental composition and crystallographic structure of the sample. The
impact of acceleration voltage can also affect the performance of these
analytical techniques.
What is TEM? What are the differences between SEM and TEM? How does sample preparation important?
TEM stands for Transmission Electron Microscopy, which is a type of
electron microscopy used to obtain high-resolution images of the internal
structure of materials and biological specimens at the nanoscale.
The basic working principle of TEM involves the transmission of a
beam of high-energy electrons through a thin sample, which interacts with the
sample, causing the electrons to scatter and diffract. The scattered electrons
are then detected and used to generate an image of the internal structure of
the sample. TEM images can provide detailed information about the crystal
structure, morphology, and defects of materials and biological specimens.
The main difference between SEM and TEM is that SEM provides images
of the surface of the sample, while TEM provides images of the internal
structure of the sample. Another key difference is that SEM uses backscattered
and secondary electrons to generate the image, while TEM uses transmitted
electrons.
Sample preparation is extremely important in TEM, as the sample
must be thin enough to allow the electrons to transmit through it. This typically
involves cutting the sample into thin sections using a microtome, and then
mounting the sections onto a thin support grid made of materials such as carbon
or copper. The thickness of the sample section can vary depending on the
application but is typically in the range of 50-200 nm.
In addition to thinning the sample, sample preparation for TEM can
also involve additional steps such as staining, which is used to enhance the
contrast between different components of the sample, and cryogenic freezing,
which is used to preserve the sample in a near-native state.
Overall, both SEM and TEM are powerful tools for investigating the
structure and properties of materials and biological specimens at the
nanoscale, and the choice of which technique to use depends on the specific
application and the type of information needed. However, sample preparation is
crucial for obtaining high-quality images and accurate results in both
techniques. Find more information here.
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