Articles you may be interested inPhoto-induced exciton generation in polyvinylpyrrolidone encapsulated Ag2S core-shells: Electrochemical deposition, regular shape and high order of particle size distribution Quasiamorphous Ag films of thicknesses ranging from 5 to 30 nm were prepared using rf magnetron sputtering technique and their controlled iodization was carried out for selected durations in the range of 15 min-60 h at room temperature. As deposited Ag and iodized films were characterized using x-ray diffraction ͑XRD͒, atomic force microscope ͑AFM͒, and optical absorption techniques. From XRD, ␥ and  + ␥ ͑mixed͒ phases of AgI nanoparticles have been observed for 5-10 and 20-30 nm thick films, respectively. Lattice parameters ͑a and c͒ and average strain ͑͒ were calculated versus iodization time for ␥ and -AgI nanoparticles. Uniform and nonuniform spherically shaped AgI nanoparticles ͑ϳ20-130 nm͒ are realized through AFM for 5-10 and 20-30 nm thick films. Optical absorption shows volume plasmons ͑classified as PR1͒ for short duration iodization, which "decay" upon further iodization to convert to Z 1,2 and Z 3 excitons at 420 and 330 nm, respectively, in the manner of a metal-semiconductor/dielectric phase transition. Ag "colloidal" particles ͑classified as PR2͒ are formed for 5 -10 nm thick films and thereby control the ␥ phase-a significant and applicable effect attributed to critical film thickness. With increasing thickness, a surface strain field lifting the degeneracy of the valence band results in Z 1,2 and Z 3 exciton formation at room temperature. Blueshift in the exciton absorption with decreasing film thickness implies the progressive quantum confinement due to decrease in the particle size. A thickness induced phase transition from ␥-AgI to -AgI is discussed by means of x-ray diffraction and optical absorption studies.