Scanning Electron Microscopy
Scanning Electron Microscopy
Scanning Electron Microscopy
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Improving Resolution<br />
• Firstly, the wavelength of the imaging source is important.<br />
In an optical microscope white light is used (λ – 380-700-nm)<br />
• In an <strong>Electron</strong> Microscope the imaging source is a beam of electrons which has a<br />
shorter wavelength (λ ~0.0025nm at 200kV) .<br />
• This is approximately five times smaller than visible light and twice as small as a<br />
typical atom – this is why electrons can ‘see’ atoms but white light can’t :-<br />
Analytical<br />
Workshop 2012<br />
‘the analysis probe must be smaller than the feature being analysed’<br />
• The wavelength of electrons is dependent on the accelerating voltage, i.e.:-<br />
kV<br />
Wavelength λ (pm)<br />
20 8.588<br />
100 3.702<br />
200 2.508<br />
300 1.968<br />
• The higher the accelerating voltage the shorter the wavelength.