Innovative transition metal catalysts prepared on the basis of preform
ed colloidal nano-particles and stabilized by surfactants are of speci
al interest with regard to industrial applications. The physical chara
cterization of the metal colloid precursors, i. e. the determination o
f their geometric and electronic structure prior to supporting, has be
en shown to be crucial for the optimization of new catalysts. Improved
activity, selectivity and resistence against deactivation in case of
bimetallic systems have been ascribed to 'synergetic effects' of the t
wo metals present in the catalytically active components. The improved
catalytic performance at a certain range of Pt:Rh atomic ratio in the
precursor can be interpreted on the basis of a geometric lattice stru
cture effect - rather than an electronic band structure effect. This h
as been shown by an investigation of both the near edge structure and
the EXAFS-region of Pt L-III X-ray absorption measurements, performed
on a series of ammonium salt stabilized bimetallic Pt/Rh resp. monomet
allic Pt colloids.