ArticleNature2010
Coherent measurements of high-order electronic correlations in quantum wells.
Article in Nature, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.
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Who cites it
17 citing papers in PubMed.
- Phase stable, shot-to-shot measurement of third- and fifth-order two-quantum correlation spectra using a pulse shaper in the pump-probe geometry.The Journal of chemical physics · 2022Article
- Frenkel biexcitons in hybrid HJ photophysical aggregates.Science advances · 2021Article
- Nonlinear rotational spectroscopy reveals many-body interactions in water molecules.Proceedings of the National Academy of Sciences of the United States of America · 2021Article
- Rapid multiple-quantum three-dimensional fluorescence spectroscopy disentangles quantum pathways.Nature communications · 2019Article
- Delocalized excitons and interaction effects in extremely dilute thermal ensembles.Physical chemistry chemical physics : PCCP · 2019Article
- Article
- Coherent multidimensional spectroscopy of dilute gas-phase nanosystems.Nature communications · 2018Article
- Biexcitons in monolayer transition metal dichalcogenides tuned by magnetic fields.Nature communications · 2018Article
- Multi-heterodyne two dimensional coherent spectroscopy using frequency combs.Scientific reports · 2017Article
- Neutral and charged inter-valley biexcitons in monolayer MoSeNature communications · 2017Article
- Advances in multi-dimensional coherent spectroscopy of semiconductor nanostructures.Advances in physics: X · 2017Article
- Nonlinear two-dimensional terahertz photon echo and rotational spectroscopy in the gas phase.Proceedings of the National Academy of Sciences of the United States of America · 2016Article
- Uncovering many-body correlations in nanoscale nuclear spin baths by central spin decoherence.Nature communications · 2014Article
- Robust excitons inhabit soft supramolecular nanotubes.Proceedings of the National Academy of Sciences of the United States of America · 2014Article
- Quantum droplets of electrons and holes.Nature · 2014Article
- Weak exciton scattering in molecular nanotubes revealed by double-quantum two-dimensional electronic spectroscopy.Physical review letters · 2012Article
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2 authors.
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No grant is acknowledged in the PubMed record.
Abstract
Strong, long-range Coulomb interactions can lead to correlated motions of multiple charged particles, which can induce important many-body effects in semiconductors. The exciton states formed from correlated electron-hole pairs have been studied extensively, but basic properties of multiple-exciton correlations-such as coherence times, population lifetimes, binding energies and the number of particles that can be correlated-are largely unknown because they are not spectroscopically accessible from the ground state. Here we present direct observations of high-order coherences in gallium arsenide quantum wells, achieved using two-dimensional multiple-quantum spectroscopy methods in which up to seven successive light fields were used. The measurements were made possible by the combination of a reconfigurable spatial beam-shaper that formed multiple beams in specified geometries and a spatiotemporal pulse-shaper that controlled the relative optical phases and temporal delays among pulses in all the beams. The results reveal triexciton coherences (correlations of three excitons or six particles), whose existence was not obvious because the third exciton spin is unpaired, and the values of their coherence times and binding energies. Rephasing of biexcitons, triexcitons and unbound two-exciton coherences was demonstrated. We also determined that there are no significant unbound correlations of three excitons and no bound or unbound four-exciton (eight-particle) correlations. Thus, the limits, as well as the properties, of many-body correlations in this system were revealed. The measurement methods open a new window into high-order many-body interactions in materials and molecules, and the present results should guide ongoing work on first-principles calculations of electronic interactions in semiconductor nanostructures.
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