Jinjun Ren

Corrosion mechanism of minerals and glass is a critical study domain in geology and materials science, vital for comprehending material durability under various environmental conditions. Despite decades of extensive study, a core aspect of these mechanisms - specifically, the formation of amorphous alteration layers upon exposure to aqueous environments - remains controversial. In this study, the corrosion behavior of a boro-alumino-phospho-silicate glass (BAPS) was investigated using advanced solid-state nuclear magnetic resonance (SSNMR) and SEM techniques. The results reveal a uniform nanoscale phase separation into Al-P-rich and Al-Si-rich domains. During corrosion, the Al-P-rich domain undergoes gelation, whereas the Al-Si-rich domain remains vitreous, forming a gel layer comprised of both phases. Although SEM images show a sharp gel/glass interface - suggestive of a dissolution-precipitation mechanism - the phase coexistence within the gel layer provides definitive evidence against such a mechanism. Instead, we propose an in situ transformation mechanism governed by chemical reactions, involving: (i) preferential hydrolysis of Al-P-rich domain leading to porous gel regions; (ii) retention of Al-Si glass domains within the gel layer, with water infiltrating inter-network spaces; and (iii) selective leaching of phosphorus over aluminum, leading to reorganization of the gel network.

Pr³⁺-doped nano-glass composites: efficient UV-C phosphors (PLQY of UV-C band: 25.93%) for disinfection and as fast scintillators (48.18 ns).