Structural transition, metallization, and superconductivity in quasi-two-dimensional layered <mml:math xmlns:mml="http://www.w3.org/1998/Math/MathML"><mml:mrow><mml:mi>Pd</mml:mi><mml:msub><mml:mi mathvariant="normal">S</mml:mi><mml:mn>2</mml:mn></mml:msub></mml:mrow></mml:math> under compression
Wen Lei, Wei Wang, Xing Ming, Shengli Zhang, Gang Tang, Xiao-Jun Zheng, Huan Li, Carmine Autieri
Abstract
Based on first-principles simulations and calculations, we explore the evolutions of crystal structure, electronic structure, and transport properties of quasi-two-dimensional layered $\mathrm{Pd}{\mathrm{S}}_{2}$ under compression by uniaxial stress and hydrostatic pressure. An interesting ferroelastic phase transition with lattice reorientation is revealed under uniaxial compressive stress, which originates from the bond reconstructions of the unusual $\mathrm{Pd}{\mathrm{S}}_{4}$ square-planar coordination. By contrast, the layered structure transforms into a three-dimensional cubic pyrite-type structure under hydrostatic pressure. In contrary to the experimentally proposed coexistence of layered $\mathrm{Pd}{\mathrm{S}}_{2}$-type structure with cubic pyrite-type structure at intermediate pressure range, we predict that the compression-induced intermediate phase will show the same structure symmetry as the ambient phase, except for sharply shrinking interlayer distances. The coordination of the Pd ions not only plays crucial roles in the structural transition, but also leads to electronic structure and transport property variations, which changes from square planar to distorted octahedron in the intermediate phase, resulting in bandwidth broadening and orbital-selective metallization. In addition, the superconductivity in the cubic pyrite-type structure comes from the strong electron-phonon coupling in the presence of topological nodal-line states. The strong interplay between structural transition, metallization, and superconductivity in $\mathrm{Pd}{\mathrm{S}}_{2}$ provides a good platform to study the fundamental physics of the interactions between crystal structure and transport behavior, and the competition or cooperation between diverse phases.