Web Release Date: January 10,
Controlled Formation of Ag Nanoparticles by Means of Long-Chain Sodium Polyacrylates in Dilute Solution
and
Contribution from the Department Chemie, Universität Paderborn, Fakultät für Naturwissenschaften, Warburger Strasse 100, D-33098 Paderborn, Germany
Received May 15, 2006
Revised Manuscript Received November 27, 2006

Abstract:
A new tool is presented to control formation of Ag nanoparticles. Small amounts of silver ions
were added to dilute solutions of long-chain sodium polyacrylates (NaPA). Four NaPA samples covering
a molar mass regime of 97 kD
Mw
650 kD have been used. With amounts of added Ag+ as low as
1-2% of the COO- groups of the polyanionic chains, significant changes could already be induced in the
NaPA coils with 650 kD. If the NaPA concentration was kept below 0.1 g/L, the coils with 650 kD exhibited
a significant coil shrinking in stable solutions. At larger NaPA concentrations, addition of Ag+ initiates an
aggregation of the polyacrylate coils toward compact structures. Coil shrinking and aggregation was revealed
by means of time-resolved static light scattering. If exposed to UV-radiation, small Ag particles formed
within the shrunken anionic polyacrylate coils. The Ag nanoparticles were identified by means of an enhanced
light scattering and a characteristic plasmon absorption band around 410 nm. No such Ag particle formation
could be observed even at 5 times larger concentrations of Ag+ and NaPA if the two smallest polyacrylate
samples have been used under otherwise equal conditions. This molar mass sensitive response of NaPA
to Ag+-addition suggests an interesting phenomenon: if the coil size of the NaPa chains, which act as Ag+
collectors, is large enough, local Ag+ concentration in these coil-shaped Ag+ containers exceeds a critical
value, and irradiation with UV generates Ag nanoparticles.
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