Search Results
Topological protection versus degree of entanglement of two-photon light in photonic topological insulators
2021, Tschernig, Konrad, Jimenez-Galán, Álvaro, Christodoulides, Demetrios N., Ivanov, Misha, Busch, Kurt, Bandres, Miguel A., Perez-Leija, Armando
Topological insulators combine insulating properties in the bulk with scattering-free transport along edges, supporting dissipationless unidirectional energy and information flow even in the presence of defects and disorder. The feasibility of engineering quantum Hamiltonians with photonic tools, combined with the availability of entangled photons, raises the intriguing possibility of employing topologically protected entangled states in optical quantum computing and information processing. However, while two-photon states built as a product of two topologically protected single-photon states inherit full protection from their single-photon “parents”, a high degree of non-separability may lead to rapid deterioration of the two-photon states after propagation through disorder. In this work, we identify physical mechanisms which contribute to the vulnerability of entangled states in topological photonic lattices. Further, we show that in order to maximize entanglement without sacrificing topological protection, the joint spectral correlation map of two-photon states must fit inside a well-defined topological window of protection.
Coherent diffractive imaging of single helium nanodroplets with a high harmonic generation source
2017, Rupp, Daniela, Monserud, Nils, Langbehn, Bruno, Sauppe, Mario, Zimmermann, Julian, Ovcharenko, Yevheniy, Möller, Thomas, Frassetto, Fabio, Poletto, Luca, Trabattoni, Andrea, Calegari, Francesca, Nisoli, Mauro, Sander, Katharina, Peltz, Christian, J. Vrakking, Marc, Fennel, Thomas, Rouzée, Arnaud
Coherent diffractive imaging of individual free nanoparticles has opened routes for the in situ analysis of their transient structural, optical, and electronic properties. So far, single-shot single-particle diffraction was assumed to be feasible only at extreme ultraviolet and X-ray free-electron lasers, restricting this research field to large-scale facilities. Here we demonstrate single-shot imaging of isolated helium nanodroplets using extreme ultraviolet pulses from a femtosecond-laser-driven high harmonic source. We obtain bright wide-Angle scattering patterns, that allow us to uniquely identify hitherto unresolved prolate shapes of superfluid helium droplets. Our results mark the advent of single-shot gas-phase nanoscopy with lab-based short-wavelength pulses and pave the way to ultrafast coherent diffractive imaging with phase-controlled multicolor fields and attosecond pulses.
Nanoplasmonic electron acceleration by attosecond-controlled forward rescattering in silver clusters
2017, Passig, Johannes, Zherebtsov, Sergey, Irsig, Robert, Arbeiter, Mathias, Peltz, Christian, Göde, Sebastian, Skruszewicz, Slawomir, Meiwes-Broer, Karl-Heinz, Tiggesbäumker, Josef, Kling, Matthias F., Fennel, Thomas
In the strong-field photoemission from atoms, molecules, and surfaces, the fastest electrons emerge from tunneling and subsequent field-driven recollision, followed by elastic backscattering. This rescattering picture is central to attosecond science and enables control of the electron's trajectory via the sub-cycle evolution of the laser electric field. Here we reveal a so far unexplored route for waveform-controlled electron acceleration emerging from forward rescattering in resonant plasmonic systems. We studied plasmon-enhanced photoemission from silver clusters and found that the directional acceleration can be controlled up to high kinetic energy with the relative phase of a two-color laser field. Our analysis reveals that the cluster's plasmonic near-field establishes a sub-cycle directional gate that enables the selective acceleration. The identified generic mechanism offers robust attosecond control of the electron acceleration at plasmonic nanostructures, opening perspectives for laser-based sources of attosecond electron pulses.
Raman gas self-organizing into deep nano-trap lattice
2016, Alharbi, M., Husakou, A., Chafer, M., Debord, B., Gérôme, F., Benabid, F.
Trapping or cooling molecules has rallied a long-standing effort for its impact in exploring new frontiers in physics and in finding new phase of matter for quantum technologies. Here we demonstrate a system for light-trapping molecules and stimulated Raman scattering based on optically self-nanostructured molecular hydrogen in hollow-core photonic crystal fibre. A lattice is formed by a periodic and ultra-deep potential caused by a spatially modulated Raman saturation, where Raman-active molecules are strongly localized in a one-dimensional array of nanometre-wide sections. Only these trapped molecules participate in stimulated Raman scattering, generating high-power forward and backward Stokes continuous-wave laser radiation in the Lamb-Dicke regime with sub-Doppler emission spectrum. The spectrum exhibits a central line with a sub-recoil linewidth as low as ∼14 kHz, more than five orders of magnitude narrower than conventional-Raman pressure-broadened linewidth, and sidebands comprising Mollow triplet, motional sidebands and four-wave mixing.