期刊
OPTICA
卷 2, 期 5, 页码 405-410出版社
OPTICAL SOC AMER
DOI: 10.1364/OPTICA.2.000405
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资金
- NCCR Molecular Ultrafast Science and Technology (NCCR MUST)
- Swiss National Science Foundation (SNSF)
- ETH Zurich Postdoctoral Fellowship Program
How quanta of energy and charge are transported on both atomic spatial and ultrafast timescales is at the heart of modern technology. Recent progress in ultrafast spectroscopy has allowed us to directly study the dynamical response of an electronic system to interaction with an electromagnetic field. Here, we present energy-dependent photoemission delays from the noble metal surfaces Ag(111) and Au(111). An interferometric technique based on attosecond pulse trains is applied simultaneously in a gas phase and a solid-state target to derive surface-specific photoemission delays. Experimental delays on the order of 100 as are in the same time range as those obtained from simulations. The strong variation of measured delays with excitation energy in Ag(111), which cannot be consistently explained invoking solely electron transport or initial state localization as supposed in previous work, indicates that final state effects play a key role in photoemission from solids. (C) 2015 Optical Society of America
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