Ultrafast probing reveals intricate dynamics of quantum coherence
Ultrafast, multidimensional spectroscopy unlocks macroscopic-scale effects of quantum electronic correlations.
Exciting the material with an ultrafast (<100fs), beam of near-infrared light produces coherent excitations lasting a surprisingly 'long' time of around 500 femtoseconds, originating from a quantum superposition of excited states within the crystal.
The strong correlation between the energy of this coherence and the optical energy of the emitted signal indicates a coherent interaction between the states at low and high energy.
This kind of coherent interaction, reported here for the first time, is the root of many intriguing and poorly-understood phenomena displayed by quantum materials.
It is one of the first applications of multidimensional spectroscopy to study of correlated electron systems such as high-temperature superconductors.
Probing quantum materials
The intriguing magnetic and electronic properties of quantum materials hold significant promise for future technologies.
However, controlling these properties requires an improved understanding of the ways in which macroscopic behaviour emerges in complex materials with strong electronic correlations.
Potentially useful electric and magnetic properties of quantum materials with strong electronic correlations include: Mott transition, colossal magnetoresistance, topological insulators, and high-temperature superconductivity.
Such macroscopic properties emerge out of microscopic complexity, rooted in the competing interactions between the degrees of freedom (charge, lattice, spin, orbital, and topology) of electronic states.
While measurements of the dynamics of excited electronic populations have been able to give some insight, they have largely neglected the intricate dynamics of quantum coherence.
In this new study, researchers applied multidimensional coherent spectroscopy to the challenge for the first time, utilising the technique's unique capability to differentiate between competing signal pathways, selectively exciting and probing low-energy excitations.
Researchers analysed the quantum coherence of excitations produced by hitting LSCO (lanthanum, strontium, copper and oxygen) crystals with a sequence of tailored, ultrafast beams of near-infrared light lasting less than 100 femtoseconds
This coherence has unusual properties, lasts a surprisingly 'long' time of around 500 femtoseconds, and originates from a quantum superposition of excited states within the crystal.
2-D spectrum showing energy difference between the states in the quantum superposition, shown before, during and after pulse overlap
"We found a strong correlation between the energy of this coherence and the optical energy of the emitted signal, which indicates a special coherent interaction between the states at low and high energy in these complex systems," says study author Jeff Davis (Swinburne University of Technology).
Because the number of available excitations affects the band structure of a crystal, the effective energy structure changes transiently during measurement, which links low-energy excitations and optically excited electronic states.
The study demonstrates that multidimensional coherent spectroscopy can interrogate complex quantum materials in unprecedented ways.
As well as representing a major advancement in ultrafast spectroscopy of correlated materials, the work has wider significance in optics/photonics, chemistry, nanoscience, and condensed-matter science.
"Persistent coherence of quantum superpositions in an optimally doped cuprate revealed by 2-D spectroscopy" was published in Science Advances in February 2020.