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    Quenching of material dependence in few-cycle driven electron acceleration from nanoparticles under many-particle charge interaction
    (London [u.a.] : Taylor & Francis, 2016-12-25) Rupp, Philipp; Seiffert, Lennart; Liu, Qingcao; Süßmann, Frederik; Ahn, Byungnam; Förg, Benjamin; Schäfer, Christian G.; Gallei, Markus; Mondes, Valerie; Kessel, Alexander; Trushin, Sergei; Graf, Christina; Rühl, Eckart; Lee, Jinwoo; Kim, Min Su; Kim, Dong Eon; Fennel, Thomas; Kling, Matthias F.; Zherebtsov, Sergey
    The excitation of nanoscale near-fields with ultrashort and intense laser pulses of well-defined waveform enables strongly spatially and temporally localized electron emission, opening up the possibility for the generation of attosecond electron pulses. Here, we investigate the electron photoemission from isolated nanoparticles of different materials in few-cycle laser fields at intensities where the Coulomb field of the ionized electrons and residual ions significantly contribute to the electron acceleration process. The dependences of the electron cut-off energy on the material’s dielectric properties and electron binding energy are investigated systematically in both experiments and semi-classical simulations. We find that for sufficiently high near-field intensities the material dependence of the acceleration in the enhanced near-fields is quenched by many-particle charge-interaction.
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    Few-cycle laser driven reaction nanoscopy on aerosolized silica nanoparticles
    ([London] : Nature Publishing Group UK, 2019) Rupp, Philipp; Burger, Christian; Kling, Nora G; Kübel, Matthias; Mitra, Sambit; Rosenberger, Philipp; Weatherby, Thomas; Saito, Nariyuki; Itatani, Jiro; Alnaser, Ali S.; Raschke, Markus B.; Rühl, Eckart; Schlander, Annika; Gallei, Markus; Seiffert, Lennart; Fennel, Thomas; Bergues, Boris; Kling, Matthias F.
    Nanoparticles offer unique properties as photocatalysts with large surface areas. Under irradiation with light, the associated near-fields can induce, enhance, and control molecular adsorbate reactions on the nanoscale. So far, however, there is no simple method available to spatially resolve the near-field induced reaction yield on the surface of nanoparticles. Here we close this gap by introducing reaction nanoscopy based on three-dimensional momentum-resolved photoionization. The technique is demonstrated for the spatially selective proton generation in few-cycle laser-induced dissociative ionization of ethanol and water on SiO2 nanoparticles, resolving a pronounced variation across the particle surface. The results are modeled and reproduced qualitatively by electrostatic and quasi-classical mean-field Mie Monte-Carlo (M3C) calculations. Reaction nanoscopy is suited for a wide range of isolated nanosystems and can provide spatially resolved ultrafast reaction dynamics on nanoparticles, clusters, and droplets.
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    Onset of charge interaction in strong-field photoemission from nanometric needle tips
    (Berlin : de Gruyter, 2021) Schötz, Johannes; Seiffert, Lennart; Maliakkal, Ancyline; Blöchl, Johannes; Zimin, Dmitry; Rosenberger, Philipp; Bergues, Boris; Hommelhoff, Peter; Krausz, Ferenc; Fennel, Thomas; Kling, Matthias F.
    Strong-field photoemission from nanostructures and the associated temporally modulated currents play a key role in the development of ultrafast vacuum optoelectronics. Optical light fields could push their operation bandwidth into the petahertz domain. A critical aspect of their functionality in the context of applications is the impact of charge interaction effects. Here, we investigated the photoemission and photocurrents from nanometric tungsten needle tips exposed to carrier-envelope phase (CEP)-controlled few-cycle laser fields. We report a characteristic rapid increase in the intensity-rescaled cutoff energies of emitted electrons beyond a certain intensity value. By comparison with simulations, we identify this feature as the onset of charge-interaction dominated photoemission dynamics. Our results are anticipated to be relevant also for the strong-field photoemission from other nanostructures, including photoemission from plasmonic nanobowtie antennas used in CEP-detection and for PHz-scale devices.
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    Nanoplasmonic electron acceleration by attosecond-controlled forward rescattering in silver clusters
    ([London] : Nature Publishing Group UK, 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.
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    Publisher Correction: Nanoplasmonic electron acceleration by attosecond-controlled forward rescattering in silver clusters (Nature communications (2017) 8 1 (1181))
    ([London] : Nature Publishing Group UK, 2018) 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
    The original PDF version of this Article contained an error in Equation 1. The original HTML version of this Article contained errors in Equation 2 and Equation 4. These errors have now been corrected in both the PDF and the HTML versions of the Article. The original PDF version of this Article contained an error in Equation 1. A dot over the first occurrence of the variable ri was missing, and incorrectly read: (Formula Presented). The correct form of Equation 1 is as follows: (Formula Presented). This has now been corrected in the PDF version of the Article. The HTML version was correct from the time of publication. The original HTML version of this Article contained errors in Equation 2 and Equation 4. In Equation 2, a circle over the first occurrence of the variable ri replaced the intended dot, and incorrectly read: (Formula Presented). The correct form of Equation 2 is as follows: (Formula Presented). In Equation 4, circles over the first and fifth occurrences of the variable ri replaced the intended dots, and incorrectly read: (Formula Presented). The correct form of Equation 4 is as follows: (Formula Presented). This has now been corrected in the HTML version of the Article. The PDF version was correct from the time of publication.