Spiral Chain O4 Form of Dense Oxygen
Li Zhu, Ziwei Wang, Yanchao Wang, Yanming Ma, Guangtian Zou and, Ho-kwang Mao

TL;DR
This paper predicts a new high-pressure phase of dense oxygen, the spiral chain O4 structure, which forms above 2 TPa and significantly alters oxygen's electronic properties from superconducting to insulating.
Contribution
It introduces a novel spiral chain O4 structure in dense oxygen, predicted through first-principles calculations, and describes its stability and electronic transition at high pressures.
Findings
O4 phase stabilizes above 2 TPa
Oxygen transitions from superconductor to insulator
O4 structure remains stable up to 2 TPa
Abstract
Oxygen is in many ways a unique element: the only known diatomic molecular magnet and the capability of stabilization of the hitherto unexpected O8 cluster structure in its solid form at high pressure. Molecular dissociations upon compression as one of the fundamental problems were reported for other diatomic solids (e.g., H2, I2, Br2, and N2), but it remains elusive for solid oxygen, making oxygen an intractable system. We here report the theoretical prediction on the dissociation of molecular oxygen into a polymeric spiral chain O4 structure (\theta-O4) by using first-principles calypso method on crystal structure prediction. The \theta-O4 stabilizes above 2 TPa and has been observed as the third high pressure phase of sulfur (S-III). We find that the molecular O8 phase remains extremely stable in a large pressure range of 0.008 - 2 TPa, whose breakdown is driven by the…
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