Abstract

Excursions far from their equilibrium structures can bring crystalline solids through collective transformations including transitions into new phases that may be transient or long-lived. Direct spectroscopic observation of far-from-equilibrium rearrangements provides fundamental mechanistic insight into chemical and structural transformations, and a potential route to practical applications, including ultrafast optical control over material structure and properties. However, in many cases photoinduced transitions are irreversible or only slowly reversible, or the light fluence required exceeds material damage thresholds. This precludes conventional ultrafast spectroscopy in which optical excitation and probe pulses irradiate the sample many times, each measurement providing information about the sample response at just one probe delay time following excitation, with each measurement at a high repetition rate and with the sample fully recovering its initial state in between measurements. Using a single-shot, real-time measurement method, we were able to observe the photoinduced phase transition from the semimetallic, low-symmetry phase of crystalline bismuth into a high-symmetry phase whose existence at high electronic excitation densities was predicted based on earlier measurements at moderate excitation densities below the damage threshold. Our observations indicate that coherent lattice vibrational motion launched upon photoexcitation with an incident fluence above 10 mJ/cm2 in bulk bismuth brings the lattice structure directly into the high-symmetry configuration for tens of picoseconds, after which carrier relaxation and diffusion restore the equilibrium lattice configuration.

Highlights

  • Crystals with symmetry-lowering Peierls distortions [1,2,3,4,5] present attractive targets for timeresolved measurements of collective transitions to new structural phases

  • Our observations indicate that coherent lattice vibrational motion launched upon photoexcitation with an incident fluence above 10 mJ=cm2 in bulk bismuth brings the lattice structure directly into the high-symmetry configuration for several picoseconds, after which carrier relaxation and diffusion restore the equilibrium lattice configuration

  • 9 mJ=cm2, the coherent phonon oscillations persist for less than a half cycle [Fig. 2(b)], indicating that the coherent lattice vibrational motion initiated upon photoexcitation through electron-phonon coupling propels the atoms directly into their positions in the high-symmetry phase

Read more

Summary

Introduction

Crystals with symmetry-lowering Peierls distortions [1,2,3,4,5] present attractive targets for timeresolved measurements of collective transitions to new structural phases. Like their molecular counterparts with Jahn-Teller distortions, Peierls-distorted systems arise due to coupling between electrons in partially filled states of nearby energy and vibrational modes along whose. Optical excitation removes electrons from those states, reducing the energy payback for vibrational distortion.

Methods
Results
Conclusion
Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call