Irradiation-induced Ag nanocluster nucleation in silicate glasses: analogy with photography
R. Espiau de Lamaestre (1, 2), H. B\'ea (1), H. Bernas (1), J., Belloni (3), J. L. Marignier (3) ((1) CSNSM-CNRS, Universit\'e Paris Sud,, Orsay, France, (2) Fontainebleau Research Center, Corning SAS, Avon, France,, (3) Laboratoire de Chimie Physique, Universit\'e Paris Sud

TL;DR
This study investigates how irradiation induces silver nanocluster formation in silicate glasses, revealing mechanisms similar to photographic latent image formation, influenced by defect interactions, redox chemistry, and energy deposition.
Contribution
It demonstrates the role of irradiation type and energy density in controlling Ag nanocluster nucleation, linking defect chemistry and redox interactions to clustering mechanisms.
Findings
Ion irradiation is more effective than gamma irradiation in inducing nanoclusters.
Cluster density depends on energy deposition and redox properties of the glass.
Mechanisms resemble latent image formation in photography.
Abstract
The synthesis of Ag nanoclusters in sodalime silicate glasses and silica was studied by optical absorption (OA) and electron spin resonance (ESR) experiments under both low (gamma-ray) and high (MeV ion) deposited energy density irradiation conditions. Both types of irradiation create electrons and holes whose density and thermal evolution - notably via their interaction with defects - are shown to determine the clustering and growth rates of Ag nanocrystals. We thus establish the influence of redox interactions of defects and silver (poly)ions. The mechanisms are similar to the latent image formation in photography: irradiation-induced photoelectrons are trapped within the glass matrix, notably on dissolved noble metal ions and defects, which are thus neutralized (reverse oxidation reactions are also shown to exist). Annealing promotes metal atom diffusion, which in turn leads to…
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