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Aggregation in colloidal gold

Journal Article · · Phys. Rev. A; (United States)
Static and dynamic light scattering are used to study the aggregation kinetics and structure of colloidal gold. Fast aggregation is achieved by either addition of pyridine, lowering of the pH, or addition of salt. The kinetics of rapid growth is followed by measurement of the polarized relaxation time tau/sub v//sub v/ (proportional to the mean cluster radius). We observe a power law, tau/sub v//sub v/proportional(Ct)/sup x/, with x = 0.38 +- 0.04, where t is the time and C is the initial sol concentration. Measurements of the depolarized relaxation time tau/sub v//sub h/ as Q..-->..0 (Q is the wave vector) are found to be proportional to the third power of the cluster radius, typical of rotational diffusion. Such measurements allow independent confirmation of the kinetics as tau/sub v//sub h/ = (Ct)/sup 3x/, with x = 0.38 +- 0.04. The static light scattering intensity I from these rapidly grown clusters obeys a power law, IproportionalQ/sup -//sup y/ with y = 1.74 +- 0.1, at a wavelength of lambda = 633 nm (optical resonance is 680 nm), with the value of y increasing away from resonance to a value of 2.0 +- 0.1 at lambda = 457 nm. Under diluted conditions the scattering behavior is identical on and off resonance with y = 2.0 +- 0.1.
Research Organization:
Sandia National Laboratories, Albuquerque, New Mexico 87185
OSTI ID:
6357429
Journal Information:
Phys. Rev. A; (United States), Journal Name: Phys. Rev. A; (United States) Vol. 39:5; ISSN PLRAA
Country of Publication:
United States
Language:
English

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