The discovery of the nonradiative decay of an inner-shell ionized atom
by the emission of an electron was made by P. Auger in 1925. The firs
t investigation of Auger electrons by means of a magnetic electron spe
ctrograph was done by Robinson and Cassie in 1926, this marks the birt
h date of Auger spectroscopy. The following 70 years of Auger spectros
copy of atoms will be divided into three periods. In the first period
(1926-1960; Section 2) Anger spectroscopy was mainly connected with be
ta-ray spectroscopy where inner-shell ionization in atoms in the solid
state was caused either by gamma-conversion or by electron capture. I
n the second period (beginning in 1960; Section 3) Auger spectroscopy
developed independently of the availability of radioactive sources by
using external excitation of gaseous atomic or metal vapor targets. Th
e third period (beginning in 1977/78; Section 4) is characterized by t
he use of synchrotron radiation with its outstanding properties of tun
ability, polarization and narrow-band high-intensity for the excitatio
n and ionization of inner-shell electrons. (C) 1998 Elsevier Science B
.V. All rights reserved.