Vídeo: Scanning Electron Microscopy SEM: Operation, Image Analysis

Scanning Electron Microscopy (SEM)

Visão Geral

Source: Laboratory of Dr. Andrew J. Steckl — University of Cincinnati

A scanning electron microscope, or SEM, is a powerful microscope that uses electrons to form an image. It allows for imaging of conductive samples at magnifications that cannot be achieved using traditional microscopes. Modern light microscopes can achieve a magnification of ~1,000X, while typical SEM can reach magnifications of more than 30,000X. Because the SEM doesn’t use light to create images, the resulting pictures it forms are in black and white.

Conductive samples are loaded onto the SEM’s sample stage. Once the sample chamber reaches vacuum, the user will proceed to align the electron gun in the system to the proper location. The electron gun shoots out a beam of high-energy electrons, which travel through a combination of lenses and apertures and eventually hit the sample. As the electron gun continues to shoot electrons at a precise position on the sample, secondary electrons will bounce off of the sample. These secondary electrons are identified by the detector. The signal found from the secondary electrons is amplified and sent to the monitor, creating a 3D image. This video will demonstrate SEM sample preparation, operation, and imaging capabilities.

Procedimento

1. Preparation of the Sample

Place sample onto sample stub. If necessary, carbon tape may be used to adhesively bond the sample to the stub.
Place the sample into a gold sputtering system. Using a mini-gold sputter, sputter gold for 30 s at ~ 70 mTorr pressure. A different gold layer thickness may be necessary depending on the geometry of the sample. More rough or porous surface requires a longer sputtering time.
Remove stub from gold sputtering system.

.css-f1q1l5{display:-webkit-box;display:-webkit-flex;display:-ms-flexbox;display:flex;-webkit-align-items:flex-end;-webkit-box-align:flex-end;-ms-flex-align:flex-end;align-items:flex-end;background-image:linear-gradient(180deg, rgba(255, 255, 255, 0) 0%, rgba(255, 255, 255, 0.8) 40%, rgba(255, 255, 255, 1) 100%);width:100%;height:100%;position:absolute;bottom:0px;left:0px;font-size:var(--chakra-fontSizes-lg);color:#676B82;}

Log in or to access full content. Learn more about your institution’s access to JoVE content here

Resultados

The SEM, seen in Figure 2a, has been used for making measurements and acquiring sample photos. The sample consisted of sodium chloride (NaCl) salt. It was placed onto the stub as seen in Figure 2b, then a few nanometers of gold was sputtered onto it to make it conductive. The conductive sample was then placed into the SEM sample area as seen in Figure 2c.

SEM images were obtained at 50X, 200X, 500X, 1,000X, and 5,000X magnification levels as s

Log in or to access full content. Learn more about your institution’s access to JoVE content here

Aplicação e Resumo

The SEM is a very powerful tool that is common in most research institutions because of its ability to image any object that is conductive, or has been treated with a conductive coating. The SEM has been used to image objects such as semiconductor devices,² biological membranes,³ and insects,⁴ among others. We have also used the SEM to analyze nanofibers and paper-based materials, biomaterials, micropatterned structures. Of course, there are materials, such as liquids, that can’t be

Log in or to access full content. Learn more about your institution’s access to JoVE content here

Referências

Goldstein, J., Newbury, D., Joy, D., Lyman, C., Echlin, P., Lifshin, E., Sawyer, L., Michael, J. Scanning Electron Microscopy and X-ray Microanalysis. 3^rd Ed. Springer, New York, NY. (2003).
Purandare, S., Gomez, E.F., Steckl, A.J. High brightness phosphorescent organic light emitting diodes on transparent and flexible cellulose films. Nanotechnology. 25, 094012 (2014).
Masuda, Y., Yamanaka, N., Ishikawa, A., Kataoka, M., Aral, T., Wakamatsu, K., Kuwahara, N., Nagahama, K., Ichikawa, K., Shimizu, A. Glomerular basement membrane injuries in IgA nephropathy evaluated by double immunostaining for a5(IV) and a2(IV) chains of type IV collagen and low-vacuum scanning electron microscopy. Clinical and Experimental Nephrology. 1-9. (2014).
Kang, J.H., Lee, Y.J., Oh, B.K., Lee, S.K. Hyun, B.R. Lee, B.W, Choi, Y.G., Nam, K.S., Lim, J.D. Microstructure of the water spider (Argyroneta aquatic) using the scanning electron microscope Journal of Asia-Pacific Biodiversity. 7 484-488 (2014).

Tags

Scanning Electron Microscopy SEM SEM Technique Electron Beam Surface Structure Analysis Chemical Composition Analysis Light Microscopy Limitations Diffraction Lateral Resolution Magnification Sub nanometer Resolution Depth Of Field SEM In Chemistry And Material Analysis Nanoscale Analysis SEM Sample Preparation SEM Operation Conductive Samples

1. Preparation of the Sample

Place sample onto sample stub. If necessary, carbon tape may be used to adhesively bond the sample to the stub.
Place the sample into a gold sputtering system. Using a mini-gold sputter, sputter gold for 30 s at ~ 70 mTorr pressure. A different gold layer thickness may be necessary depending on the geometry of the sample. More rough or porous surface requires a longer sputtering time.
Remove stub from gold sputtering system.

2. Sample Insertion and SEM Startup

Vent the SEM chamber, allowing the chamber to reach nominal pressure.
Open the SEM sample compartment and take out the sample stage.
Insert the sample stub containing the sample onto the stage. Tighten the stub into place.
If the z-distance cannot be controlled by software, make sure the sample stage with sample stub has proper height to obtain the better image.
Put the sample stage into sample chamber. Close the sample compartment.
Turn on the pumps and allow system to reach vacuum. The system will notify the user when this is completed.
Open the SEM software. Select desired operating voltage ranging from 1–30 kV. Higher operating voltage gives better image contrast, but can yield lower resolution if charges accumulate in the sample.

3. Capturing the SEM Image

Begin ‘Auto Focus’ in the SEM software by clicking on the key icon. This will acquire a focused image of the sample to use as a starting point.
Make sure the magnification is set to the minimum zoom level of 50X.
Select ‘fast scan’ mode.
Adjust the focus in coarse mode until a rough focus is acquired.
Adjust the stage manually using the exterior knobs so that the region of interest is visible on the display.
Increase the magnification level until the desired feature is observed. Adjust the coarse focusing knob to roughly focus the image at this magnification. Then, improve the focus using the fine focusing knob to get a focused image at the desired magnification level. This step will be repeated whenever the magnification level is increased.
Once the desired magnification is reached, adjust the fine focusing knob to improve clarity.
To optimize image clarity, increase the magnification close to the maximum level, and then focus the image using the fine focus knob. If a clear image cannot be obtained, adjust the stigmation in both the x and y direction. Keep adjusting the focus and stigmations until the clearest image is obtained at the exaggerated magnification level.
After reaching a quality image of the sample, go back to the desired magnification level. The image can be taken by pressing the photo button in either ‘slow photo’ or ‘fast photo’ mode. The ‘slow photo’ mode gives better quality and high resolution of the image.

4. Making Measurements Using the SEM Software

In the ‘Panels’ dropdown list, select ‘M. Tools’.
Various measurements such as length, area, and angle can be measured directly in the SEM software. To perform one of these measurements, click on the desired icon in the M. Tools window.
Scroll to the measurement site on the SEM image. Measurements are done by clicking on the image to create points of reference that will be analyzed by the software. Data points measured can be inserted directly onto the image if desired by the user.
Images are then saved to the computer.

Pular para...

0:00

Overview

1:49

Principles of Scanning Electron Microscopy

4:10

Sample Preparation and Loading

5:54

SEM Operation

8:22

Image Analysis

9:17

Applications

11:13

Summary

Vídeos desta coleção:

article

Now Playing

Scanning Electron Microscopy (SEM)

Analytical Chemistry

86.6K Visualizações

article

Preparação da Amostra para Caracterização Analítica

Analytical Chemistry

83.7K Visualizações

article

Normas Internas

Analytical Chemistry

203.3K Visualizações

article

Método de adição de padrão

Analytical Chemistry

318.8K Visualizações

article

Curvas de calibração

Analytical Chemistry

789.0K Visualizações

article

Espectroscopia ultravioleta-visível (UV-Vis)

Analytical Chemistry

616.4K Visualizações

article

Espectroscopia raman para análise química

Analytical Chemistry

50.8K Visualizações

article

Fluorescência de raios X (XRF)

Analytical Chemistry

25.3K Visualizações

article

Cromatografia gasosa (GC) com detecção por ionização em chama

Analytical Chemistry

279.8K Visualizações

article

Cromatografia Líquida de Alta Eficiência (HPLC)

Analytical Chemistry

381.8K Visualizações

article

Cromatografia de troca iônica

Analytical Chemistry

263.0K Visualizações

article

Eletroforese Capilar (CE)

Analytical Chemistry

93.0K Visualizações

article

Introdução à Espectrometria de Massa

Analytical Chemistry

111.4K Visualizações

article

Medições eletroquímicas de catalisadores suportados usando um potenciostato/galvanostato

Analytical Chemistry

51.2K Visualizações

article

Voltametria Cíclica (CV)

Analytical Chemistry

123.4K Visualizações

Copyright © 2025 MyJoVE Corporation. Todos os direitos reservados