Growth Mechanisms of Silver Halide Clusters from the Molecule to the Colloidal Particle

Article abstract of DOI:10.1021/j100353a031

Studies of growing silver halide clusters, from the molecular level to colloidal-size particles, have been undertaken and correlations between particle size and physical properties have been investigated.The production of halide ions by dissociative electron attachement following pulse radiolysis of methylene halide solutions was utilized to instantaneously produce homogeneous, supersaturated solutions of halide and silver ions.The grows of silver halide particles in these solutions has been examined by conductance, absorption spectroscopy, and light scattering measurements.Conductivity measurements show that the initial reaction between the ions occurs at a diffusion-controlled rate and allow determination of the stability constants of molecular silver halide species.In solutions containing excess silver ions, particle growth of silver iodide and bromide occurs via a diffusion-controlled aggregation mechanism during the first seconds.The grows rate is reduced significantly, due to electrostatic repulsion between particles, when the concentation of halide ions is almost equal to or greater than the stoichiometric concentration of silver ions.The absorbance of silver iodide suspensions produced in this manner has also been measured.The initial absorbance, due to AgI molecules, occurs at wavelengths of 280 nm and below.The lowest energy excitation band appears ca. 50 μs after initiation of the reaction.This band initially peaks at around 320 nm and shifts toward 425 nm (the wavelength of excitation absorption in bulk silver iodide).The surface potential at the interface evolves at about the same rate as the bulk properties of the material.For the mostly dissociated AgCl molecules growth by addition of ions to a small number of particles of critical size was observed.