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1998
DOI: 10.1016/s0009-2614(97)01445-0
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Spectroscopic investigation of silver in soda-lime glass

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Cited by 89 publications
(75 citation statements)
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“…The different duration of the current rise, depending on the metal, must be ascribed to the different chemical behavior of the metals at the interface. At present, no evidence for the formation of metallic or oxide nanoclusters can be supported by our experimental data: the shape of diffusion profiles indicates diffusion mechanism that do not involve the formation of clusters, a situation similar to those already reported for Cu and Ag migration [13,14], for which more mobile ion species (Cu + and Ag + ) do not however give rise to clusterization, at even higher temperatures in the case of Cu.…”
Section: Resultssupporting
confidence: 48%
“…The different duration of the current rise, depending on the metal, must be ascribed to the different chemical behavior of the metals at the interface. At present, no evidence for the formation of metallic or oxide nanoclusters can be supported by our experimental data: the shape of diffusion profiles indicates diffusion mechanism that do not involve the formation of clusters, a situation similar to those already reported for Cu and Ag migration [13,14], for which more mobile ion species (Cu + and Ag + ) do not however give rise to clusterization, at even higher temperatures in the case of Cu.…”
Section: Resultssupporting
confidence: 48%
“…In most of the related studies, characteristic surface-plasmon-resonance (SPR) of silver nanoparticles have always been given the maximum importance due to the fast optical response (~few psec) of nanoscale metal particles in the visible range of light [9,10]. In spite of the technological significance, precise spectroscopic studies to characterize the thermal stability of these optical nanomaterials are still only successful to a limited extent [11][12][13].…”
mentioning
confidence: 99%
“…The former peak is ascribed to the spin-allowed electronic transitions from the 1 D 2 state to the ground 1 S 0 state of the Ag ions and the latter peak to the spin-forbidden electronic transition from the 3 D manifold state to the 1 S 0 state. 13 The peak intensity initially increased with increasing n from 1 to 6, then decreased with n 6 to 12, and finally the luminescence vanished at nŊ24. For samples Ag-320-n Fig.…”
Section: Visual Observation and Optical Absorption Spectramentioning
confidence: 92%