Topological Signatures of Hardness and Structural Order in Network-Forming Materials

Abstract

Understanding how the topology of network forming materials influences their physical properties remains a longstanding challenge. Here, we investigate the topology of experimentally compatible atomistic models of amorphous silica together with the crystalline polymorphs cristobalite and quartz. By comparing multiple atomistic models of amorphous silica that equally reproduce neutron-scattering data, we show that different microscopic descriptions can imply different topological interpretations of glass stability. To characterize the network beyond conventional geometric descriptors, we introduce the linking valence, which quantifies the average number of topological links per network loop. This topological descriptor separates silica into two distinct classes: the mechanically harder quartz exhibit values more than an order of magnitude larger than those of amorphous silica and cristobalite, despite their common tetrahedral building blocks. Spectral analysis of the loop-linking networks provides a complementary distinction, separating amorphous from crystalline phases and revealing differences in the long-range organization of topological constraints. These results establish topological linking as a new framework for connecting the structure and physical properties of network-forming materials.