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Field propagation-induced directionality of carrier-envelope phase-controlled photoemission from nanospheres

Near-fields of non-resonantly laser-excited nanostructures enable strong localization of ultrashort light fields and have opened novel routes to fundamentally modify and control electronic strong-field processes. Harnessing spatiotemporally tunable near-fields for the steering of sub-cycle electron...

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Detalles Bibliográficos
Autores principales: Süßmann, F., Seiffert, L., Zherebtsov, S., Mondes, V., Stierle, J., Arbeiter, M., Plenge, J., Rupp, P., Peltz, C., Kessel, A., Trushin, S. A., Ahn, B., Kim, D., Graf, C., Rühl, E., Kling, M. F., Fennel, T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Pub. Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4557130/
https://www.ncbi.nlm.nih.gov/pubmed/26264422
http://dx.doi.org/10.1038/ncomms8944
Descripción
Sumario:Near-fields of non-resonantly laser-excited nanostructures enable strong localization of ultrashort light fields and have opened novel routes to fundamentally modify and control electronic strong-field processes. Harnessing spatiotemporally tunable near-fields for the steering of sub-cycle electron dynamics may enable ultrafast optoelectronic devices and unprecedented control in the generation of attosecond electron and photon pulses. Here we utilize unsupported sub-wavelength dielectric nanospheres to generate near-fields with adjustable structure and study the resulting strong-field dynamics via photoelectron imaging. We demonstrate field propagation-induced tunability of the emission direction of fast recollision electrons up to a regime, where nonlinear charge interaction effects become dominant in the acceleration process. Our analysis supports that the timing of the recollision process remains controllable with attosecond resolution by the carrier-envelope phase, indicating the possibility to expand near-field-mediated control far into the realm of high-field phenomena.