Raman scattering experiments have been carried out to study persistent densification in SiO(2) glass following hydrostatic compression at room temperature. A new relationship linking selective Raman parameters to the degree of densification in the glass has been developed here. This approach will allow quantification of the residual densification in silica following microindentation experiments, with the goal being the development of a constitutive law for amorphous silica.

The elastic and plastic behaviors of silica glasses densified at various maximum pressure reached (12 GPa, 15 GPa, 19 GPa, and 22 GPa), were analyzed using in situ Raman and Brillouin spectroscopies. The elastic anomaly was observed to progressively vanish up to a maximum pressure reached of 12 GPa, beyond which it is completely suppressed. Above the elastic anomaly the mechanical behavior of silica glass, as derived from Brillouin measurements, is interpreted in terms of pressure induced transformation of low density amorphous silica into high density amorphous silica.

Density changes of GeO 2 and SiO 2 glasses subjected to irradiation by tightly focused femtosecond pulses are observed by Raman scattering. It is shown that densification caused by the void formation in GeO 2 glass is very similar to the changes under hydrostatic pressure. In contrast, the experimental observations in SiO 2 glass could be explained by pressure effect or by the fictive temperature anomaly, i. e., a resultant smaller specific volume of the glass (a denser phase) at a high thermal quenching rate. Density changes of GeO 2 and SiO 2 glasses are opposite upon close-to-equilibrium heating; this gives new insights into the mechanisms of densification under highly non-equilibrium conditions: fs-laser induced micro-explosions, heating and void formation. The pressure and temperature effects of glass modification by ultra-short laser pulses are discussed considering applications in optical memory, waveguiding, and formation of micro-optical elements.

The in situ elastic and plastic behaviors of sodium aluminosilicate glasses with different degrees of depolymerization were analyzed using Brillouin spectroscopy. The observed elastic anomaly progressively vanished with depolymerization. The densification process appears to be different from that observed in pure silica glass. In the plastic regime of densified glasses hysteresis loops were observed and related to modification of the local silicon environment facilitated by the addition of sodium.

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