Exceptional phonon point versus free phonon coupling in Zn1-xBexTe under pressure: an experimental and ab initio Raman study

Raman scattering and ab initio Raman/phonon calculations, supported by X-ray diffraction, are combined to study the vibrational properties of Zn1-xBexTe under pressure. The dependence of the Be-Te (distinct) and Zn-Te (compact) Raman doublets that distinguish between Be- and Zn-like environments is examined within the percolation model with special attention to x similar to (0,1). The Be-like environment hardens faster than the Zn-like one under pressure, resulting in the two sub-modes per doublet getting closer and mechanically coupled. When a bond is so dominant that it forms a matrix-like continuum, its two submodes freely couple on crossing at the resonance, with an effective transfer of oscillator strength. Post resonance the two submodes stabilize into an inverted doublet shifted in block under pressure. When a bond achieves lower content and merely self-connects via (finite/infinite) treelike chains, the coupling is undermined by overdamping of the in-chain stretching until a ''phonon exceptional point'' is reached at the resonance. Only the out-of-chain vibrations ''survive'' the resonance, the in-chain ones are ''killed''. This picture is not bond-related, and hence presumably generic to mixed crystals of the closing-type under pressure (dominant over the opening-type), indicating a key role of the mesostructure in the pressure dependence of phonons in mixed crystals.

Automated summary

The vibrational properties of Zn1-xBexTe under pressure were studied using Raman scattering and ab initio Raman/phonon calculations. The study found that the Be-like environment hardens faster than the Zn-like one under pressure, resulting in the closer proximity and mechanical coupling of the two sub-modes per doublet. It was also observed that when a bond forms a matrix-like continuum, its two submodes can freely couple and stabilize into an inverted doublet under pressure, while in-chain vibrations are "killed" at resonance when the bond merely self-connects via treelike chains.