F. Henglein et al., SURFACE-CHEMISTRY OF COLLOIDAL GOLD - DEPOSITION AND REOXIDATION OF PB, CD, AND TL, Berichte der Bunsengesellschaft fur Physikalische Chemie, 98(2), 1994, pp. 180-189
Citations number
27
Categorie Soggetti
Chemistry Physical
Journal title
Berichte der Bunsengesellschaft fur Physikalische Chemie
Lead, cadmium and thallium are deposited on colloidal gold particles i
n aqueous solution. The deposition occurs through the reduction of the
metal ions by excess electrons which are donated to the gold particle
s by free organic radicals generated radiolytically. The absorption sp
ectra of the composite particles are measured and compared to calculat
ed ones (using Mie theory and the optical constants of the pure metals
). - Au-Pb particles are stable and well separated, and there is reaso
nable agreement between experimental and calculated spectra. Reoxidati
on of the lead mantle by Ag+ ions leads to a silver mantle, although a
bout 5% of the deposited lead is not oxidized; this is attributed to t
he strong binding of Pb adatoms to the gold surface. The reoxidation o
f Pb adatoms by Ag+ occurs much more slowly than the oxidation of indi
vidual Pb(n) particles, which is attributed to the more electropositiv
e nature of the deposited metal. - Au-Cd particles tend to agglomerate
, especially when the Cd mantle is reoxidized by Ag+ ions. The resulti
ng Au-Ag particles contain a large percentage of non-oxidized cadmium;
alloy formation seems to be a possible explanation. - The spectra of
Au-Tl particles are not in good agreement with the calculated ones; it
seems that the reduced Tl does not form an even mantle around the Au(
n) particles.