Pressure-induced polyamorphism in TiO2 nanoparticles
Denis Machon, Marlène Daniel, Vittoria Pischedda, S. Danièle, Pierre Bouvier, Sylvie Le Floch
Abstract
Open-access reader
Denis Machon, Marlène Daniel, Vittoria Pischedda, S. Danièle, Pierre Bouvier, Sylvie Le Floch
Abstract
Open-access reader
Two different nanometric (6 nm) ${\text{TiO}}_{2}$ compounds, anatase polycrystals and amorphous particles, were investigated under high pressure using Raman spectroscopy. Nanoanatase undergoes a pressure-induced amorphization. The pressure-induced transformations of this mechanically prepared amorphous state are compared with those of a chemically prepared amorphous particles. In the mechanically prepared amorphous state, a reversible transformation from a low-density amorphous state to high-density amorphous state (HDA1) is observed in the range 13--16 GPa. In the chemically prepared sample, a transformation to a new high-density amorphous state (HDA2) is observed at around 21 GPa. Further compression leads to the transformation $\text{HDA}2\ensuremath{\rightarrow}\text{HDA}1$ at $\ensuremath{\sim}30\text{ }\text{GPa}$. We demonstrate that depending on the starting amorphous material, the high-pressure polyamorphic transformations may differ. This observation indicates that pressure is a suited tool to discriminate between nanomaterials apparently similar at ambient conditions.
OpenAlex reports 44 citations for this work. Citation counts describe recorded attention and do not establish research quality.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
Two different nanometric (6 nm) ${\text{TiO}}_{2}$ compounds, anatase polycrystals and amorphous particles, were investigated under high pressure using Raman spectroscopy. Nanoanatase undergoes a pressure-induced amorphization. The pressure-induced transformations of this mechanically prepared amorphous state are compared with those of a chemically prepared amorphous particles. In the mechanically prepared amorphous state, a reversible transformation from a low-density amorphous state to high-density amorphous state (HDA1) is observed in the range 13--16 GPa. In the chemically prepared sample, a transformation to a new high-density amorphous state (HDA2) is observed at around 21 GPa. Further compression leads to the transformation $\text{HDA}2\ensuremath{\rightarrow}\text{HDA}1$ at $\ensuremath{\sim}30\text{ }\text{GPa}$. We demonstrate that depending on the starting amorphous material, the high-pressure polyamorphic transformations may differ. This observation indicates that pressure is a suited tool to discriminate between nanomaterials apparently similar at ambient conditions.
Key concepts: Amorphous solid, Polyamorphism, Anatase, Materials science, Raman spectroscopy, High pressure, Crystallography, Analytical Chemistry (journal)