Aeschlimann, Martin and Bange, Jan Philipp and Bauer, Michael and Bovensiepen, Uwe and Elmers, Hans-Joachim and Fauster, Thomas and Gierster, Lukas and Hoefer, Ulrich and Huber, Rupert and Li, Andi and Li, Xintong and Mathias, Stefan and Morgenstern, Karina and Petek, Hrvoje and Reutzel, Marcel and Rossnagel, Kai and Schoenhense, Gerd and Scholz, Markus and Stadtmueller, Benjamin and Staehler, Julia and Tan, Shijing and Wang, Bing and Wang, Zehua and Weinelt, Martin (2025) Time-resolved photoelectron spectroscopy at surfaces. SURFACE SCIENCE, 753: 122631. ISSN 0039-6028, 1879-2758
Full text not available from this repository. (Request a copy)Abstract
Light is a preeminent spectroscopic tool for investigating the electronic structure of surfaces. Time-resolved photoelectron spectroscopy has mainly been developed in the last 30 years. It is therefore not surprising that the topic was hardly mentioned in the issue on "The first thirty years"of surface science. In the second thirty years, however, we have seen tremendous progress in the development of time-resolved photoelectron spectroscopy on surfaces. Femtosecond light pulses and advanced photoelectron detection schemes are increasingly being used to study the electronic structure and dynamics of occupied and unoccupied electronic states and dynamic processes such as the energy and momentum relaxation of electrons, charge transfer at interfaces and collective processes such as plasmonic excitation and optical field screening. Using spin- and time-resolved photoelectron spectroscopy, we were able to study ultrafast spin dynamics, electron-magnon scattering and spin structures in magnetic and topological materials. Light also provides photon energy as well as electric and magnetic fields that can influence molecular surface processes to steer surface photochemistry and hot-electron-driven catalysis. In addition, we can consider light as a chemical reagent that can alter the properties of matter by creating non-equilibrium states and ultrafast phase transitions in correlated materials through the coupling of electrons, phonons and spins. Electric fields have also been used to temporarily change the electronic structure. This opened up new methods and areas such as high harmonic generation, light wave electronics and attosecond physics. This overview certainly cannot cover all these interesting topics. But also as a testimony to the cohesion and constructive exchange in our ultrafast community, a number of colleagues have come together to share their expertise and views on the very vital field of dynamics at surfaces. Following the introduction, the interested reader will find a list of contributions and a brief summary in Section 1.3.
| Item Type: | Article |
|---|---|
| Uncontrolled Keywords: | CORE-LEVEL PHOTOEMISSION; HIGH-HARMONIC GENERATION; IMAGE-POTENTIAL STATES; FLOQUET-BLOCH STATES; 2-PHOTON PHOTOEMISSION; ELECTRON DYNAMICS; ULTRAFAST DYNAMICS; ANGULAR-MOMENTUM; BAND-STRUCTURE; X-RAY; Time-resolved photoemission; Image-potential states; Time-resolved photoemission electron; microscopy; Hot electron dynamics; Plasmons; Semiconductor heterostructures; Photostationary states; Time-and spin-resolved photoemission; Ultrafast spin dynamics; Magnons; Femtomagnetism; Time-resolved momentum microscopy; Exciton dynamics; Dark exciton; Interlayer exciton; Intervalley scattering; Momentum microscope; Scherzer theorem; Free-electron laser |
| Subjects: | 500 Science > 530 Physics |
| Divisions: | Physics > Institute of Experimental and Applied Physics > Chair Professor Huber > Group Rupert Huber |
| Depositing User: | Dr. Gernot Deinzer |
| Date Deposited: | 07 Apr 2026 11:52 |
| Last Modified: | 07 Apr 2026 11:52 |
| URI: | https://pred.uni-regensburg.de/id/eprint/65649 |
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