The electronic properties of correlated mixed-valent Ce compounds have
been studied in detail over the last two decades by means of a variet
y of electron spectroscopies. This work has been carried out in connec
tion with their peculiar ground state properties, deriving from the hy
bridization of the Ce 4f wavefunctions with the conduction band states
. However, the relevance of surface effects, in the interpretation of
the spectral line-shapes has been recognized only very recently. These
are related to the reduction of 4f hybridization at the surface. In t
his review I will give a summary of the main achievements in this area
, showing the procedures to separate the surface from the bulk spectra
l contributions for both the Ce 4f spectral functions and the Ce 3d co
re levels. In addition, a systematic analysis of the surface and bulk
electronic properties of a number of different compounds is reported.
This new information can in some cases reconcile the results obtained
by different spectroscopies in terms of theoretical models based on th
e Anderson single impurity Hamiltonian. However, when comparing spectr
oscopies which rise to considerably different final states this may no
longer be valid and some possible solutions are outlined. Furthermore
, preliminary results on single crystals are presented. They seem to s
how somewhat unexpected features which need to be studied in deeper de
tail in the future. (C) 1998 Elsevier Science B.V.