• Plönjes, Elke
• Mann, Klaus
• Palo, Nicola Di
• Mey, Tobias
• Reduzzi, Maurizio
• Chien, Ying-Hao
• León, Iker
• Buades, Bárbara
• Sun, Hung-Wei
• Sidiropoulos, Themistoklis P. H.
• Schwoerer, Heinrich
• Teichmann, Stephan M.
• Summers, Adam M.
• Severino, Stefano
• Biegert, Jens
• Rivas, Daniel E.
• Keitel, Barbara
• Efetov, Dmitri K.
• Cousin, Seth L.

Abstract

<jats:p>Unraveling the exact nature of nonequilibrium and correlated interactions is paramount for continued progress in many areas of condensed matter science. Such insight is a prerequisite to develop an engineered approach for smart materials with targeted properties designed to address standing needs such as efficient light harvesting, energy storage, or information processing. For this goal, it is critical to unravel the dynamics of the energy conversion processes between carriers in the earliest time scales of the excitation dynamics. We discuss the implementation and benefits of attosecond soft x-ray core-level spectroscopy up to photon energies of 600 eV for measurements in solid-state systems. In particular, we examine how the pairing between coherent spectral coverage and temporal resolution provides a powerful new insight into the quantum dynamic interactions that determine the macroscopic electronic and optical response. We highlight the different building blocks of the methodology and point out the important aspects for its application from condensed matter studies to materials as thin as 25 nm. Furthermore, we discuss the technological developments in the field of tabletop attosecond soft x-ray sources with time-resolved measurements at the near and extended edge simultaneously and investigate the exciting prospective of extending such technique to the study of 2-dimensional materials.</jats:p>

Topics

• impedance spectroscopy
• X-ray spectroscopy