Since the early years of Ii-ray spectrometry in electron microscopes, mappi
ng the locations of chemical elements has been important. The X-rays needed
in large numbers for this are rare, owing to poor production efficiency co
mpared with electron signals, and at risk of loss by many mechanisms such a
s missing the limited solid angle of the detector, absorption before reachi
ng the detector and pulse pile-up conventional digital mapping hardware red
uces the information contained in the X-ray spectrum at each pixel to the i
tegrated counts from a few regions of interest.
The acquisition technique of position-tagged spectrometry eliminates the co
nflict between the desire to see full frame Ii-ray images quickly versus th
e analytical advantages of having complete spectra for each pixel. As the b
eam is scanned rapidly relative to traditional Ii-ray mapping, photons are
counted in a virtual 3-D multichannel analyser on disk, preserving both spa
tial and spectral information. Along with the sophisticated post-processing
allowed by storing an entire spectrum per pixel, a unique degree of dynami
c interaction with the developing data is made possible by integrating many
short scans instead of using a single long dwell time at each pixel.