How optical excitation controls the structure and properties of vanadium dioxide

TL;DR

This study uses ultrafast diffraction and spectroscopy to explore how optical excitation induces phase transitions in vanadium dioxide, revealing the structure of a metastable monoclinic metal phase and its impact on electronic properties.

Contribution

It provides the first detailed characterization of a photoinduced monoclinic metal phase in VO2 and links ultrafast structural changes to electronic transport phenomena.

Findings

Identification of a metastable monoclinic metal phase with anti-ferroelectric charge order.

Demonstration of distinct contributions of monoclinic and rutile phases to conductivity changes.

Highlighting the importance of multi-modal experiments for understanding ultrafast phase transitions.

Abstract

We combine ultrafast electron diffraction and time-resolved terahertz spectroscopy measurements to unravel the connection between structure and electronic transport properties during the photoinduced insulator-metal transitions in vanadium dioxide. We determine the structure of the metastable monoclinic metal phase, which exhibits anti-ferroelectric charge order arising from a thermally activated, orbital-selective phase transition in the electron system. The relative contribution of this photoinduced monoclinic metal (which has no equilibrium analog) and the photoinduced rutile metal (known from the equilibrium phase diagram) to the time and pump-fluence dependent multi-phase character of the film is established, as is the respective impact of these two distinct phase transitions on the observed changes in terahertz conductivity. Our results represent an important new example of how light can control the properties of strongly correlated materials and elucidate that multi-modal experiements are essential when seeking a detailed connection between ultrafast changes in optical-electronic properties and lattice structure in complex materials.