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Attosecond Electron Correlation and Molecular Resonance in \textit{K}-shell Photoexcitation of Nitric Oxide

ORAL

Abstract

Angular streaking is employed to resolve the attosecond electronic motion of nitric oxide (NO) irradiated with intense, sub-femtosecond, soft X-ray pulses from a free-electron laser.\footnote{Duris, Li \textit{et al.}, Nat. Phot. \textbf{14}, 30 (2020)} We scan the incident photon energy through the O \textit{K}-edge and measure the dynamics of the resultant photoemission. Below the edge we drive the O $1s \rightarrow 2p\pi ^\ast$ core excitation and time-resolve the subsequent electron correlation-driven Auger decay. Above the \textit{K}-edge we measure the photon energy-dependent dynamics determining the precise release time of the O \textit{K}-shell electron into the continuum. We observe the attosecond time-delay associated with the O $1s \rightarrow 2p\sigma ^\ast$ shape resonance previously identified in cross-section measurements.

Authors

  • Taran Driver

    Stanford PULSE Institute/LCLS

  • Elio G. Champenois

    SLAC National Accelerator Laboratory, Stanford PULSE Institute, SLAC National Accelerator Laboratory, Stanford PULSE Institute/LCLS

  • James Cryan

    SLAC National Accelerator Laboratory, Stanford PULSE Institute, SLAC National Accelerator Laboratory, Stanford PULSE Institute/LCLS

  • Siqi Li

    SLAC National Accelerator Laboratory, SLAC Natl. Accelerator Lab.

  • Agostino Marinelli

    SLAC National Accelerator Laboratory, SLAC - Natl Accelerator Lab, SLAC Natl. Accelerator Lab.

  • Philipp Rosenberger

    MPQ/LMU Munich

  • M.F. Kling

    MPQ/LMU Munich, LMU, Munich; MPQ

  • Lisa Ortmann

    The Ohio State University, Ohio State University

  • Alexandra Landsman

    The Ohio State University, Ohio State University