Pathways of bond topology transitions at the interface of silicon nanocrystals and amorphous silica matrix

TL;DR

This study uses molecular dynamics to explore the complex bond topology transitions at silicon nanocrystal interfaces with amorphous silica, revealing new oxygen complexes and strain behaviors not previously documented.

Contribution

It uncovers previously unnoted three-coordinated oxygen complexes and details the evolution of interface bond topology in silicon nanocrystals embedded in silica.

Findings

Identification of new three-coordinated oxygen complexes.

Absence of double bonds at the interface.

Strain localized at the nanocrystal surface.

Abstract

The interface chemistry of silicon nanocrystals (NCs) embedded in amorphous oxide matrix is studied through molecular dynamics simulations with the chemical environment described by the reactive force field model. Our results indicate that the Si NC-oxide interface is more involved than the previously proposed schemes which were based on solely simple bridge or double bonds. We identify different types of three-coordinated oxygen complexes, previously not noted. The abundance and the charge distribution of each oxygen complex is determined as a function of the NC size as well as the transitions among them. The oxidation at the surface of NC induces tensile strain to Si-Si bonds which become significant only around the interface, while the inner core remains unstrained. Unlike many earlier reports on the interface structure, we do not observe any double bonds. Furthermore, our simulations and analysis reveal that the interface bond topology evolves among different oxygen bridges through these three-coordinated oxygen complexes.