ORGANIZATION OF AU COLLOIDS AS MONOLAYER FILMS ONTO ITO GLASS SURFACES - APPLICATION OF THE METAL COLLOID FILMS AS BASE INTERFACES TO CONSTRUCT REDOX-ACTIVE MONOLAYERS
A. Doron et al., ORGANIZATION OF AU COLLOIDS AS MONOLAYER FILMS ONTO ITO GLASS SURFACES - APPLICATION OF THE METAL COLLOID FILMS AS BASE INTERFACES TO CONSTRUCT REDOX-ACTIVE MONOLAYERS, Langmuir, 11(4), 1995, pp. 1313-1317
Au colloid films are organized on indium tin oxide (ITO) surfaces usin
g (aminopropyl)siloxane or (mercaptopropyl)siloxane as base monolayer
for the deposition of the metal colloid. Different Au colloids, rangin
g in particles of diameters 25, 30, 35, and 120 nm, were deposited on
the monolayer-modified ITO surfaces. For the small particles, 25 nm, a
n almost continuous Au colloid film is formed with interparticle spaci
ng of 10-25 nm. The surface coverage of the Au colloid on the (aminopr
opyl)siloxane monolayer is higher than that for the (mercaptopropyl)si
loxane-modified ITO. The Au colloid films provide active surfaces for
the self-assembly of redox-active thiolate monolayers. 8-(N-Methyl-4,4
'-bipyridinyl)octanoic acid was covalently linked to a cystamine monol
ayer assembled onto the Au colloids. For the 25-nm Au colloid the surf
ace coverage by the redox active unit, 6.8 x 10(-10) mol cm(-2), is ca
. 12-fold higher than that of the (aminopropyl)siloxane monolayer-modi
fied ITO, lacking the Au film. The surface coverages of the Au colloid
films by the bipyridinium monolayers increase as the colloid particle
sizes decrease.