Proceedings of the 8th International Conference on Attosecond Science and Technology
Proceedings of the 8th International Conference on Attosecond Science and Technology
Chini, Michael; Fang, Li; Argenti, Luca
Springer International Publishing AG
03/2024
220
Mole
Inglês
9783031479403
15 a 20 dias
Descrição não disponível.
Chapter 1. Single-cycle infrared waveform generation and control.- Chapter 2. Increase in Photon Flux of Attosecond Pulses.- Chapter 3. Bright coherent XUV generation in microfluidic glass devices for ultrafast x-ray spectroscopy.- Chapter 4. Attosecond Physics and Quantum Information Science.- Chapter 5. Dynamics via Attosecond Four-Wave Mixing.- Chapter 6. Optical control of autoionizing states in argon.- Chapter 7. Retrieving a Complex Molecular Structure from Laser-Induced Electron Diffraction using Ma-chine Learning.- Chapter 8. Imaging ultrafast Dissociation Dynamics: OCS & Roaming in Formaldehyde.- Chapter 9. Controlling the time evolution of electron-nuclei entanglement for steering vibronic coherences dynamics induced by short 1-2 fs optical pulses.- Chapter 10. An MQDT model for the description of time resolved pump probe experiments.- Chapter 11. ASTRA, A Transition Density Matrix Approach to the Interaction of Attosecond Radiation with Atoms and Molecules.- Chapter 12. Symmetry-protected chiral sensitivity in photoionization with bichromatic fields.- Chapter 13. Experimental investigation of topological property of degenereate singularities in rescattering processes.- Chapter 14. Simulating strong field tunnel ionization of molecules.- Chapter 15. Control of photoelectron-ion entanglement in attosecond laser-induced photoionization of H2.- Chapter 16. Ultrafast Second-harmonic XUV Spectroscopy: A Novel Probe for Symmetry.- Chapter 17. From Ultrafast Light-Induced Currents to Spatially-Resolved Field Sampling.- Chapter 18. Attosecond core-exciton dynamics in wide-gap insulators.- Chapter 19. Polarization-Shaped Strong Field Control over Valley Polarization with Mid-IR Light.- Chapter 20. The Future of Attosecond Science.
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attosecond physics;high-harmonic generation;free-electron laser;pump-probe spectroscopy;strong-field physics;ultrafast electron dynamics;sub-femtosecond XUV pulse;open access
Chapter 1. Single-cycle infrared waveform generation and control.- Chapter 2. Increase in Photon Flux of Attosecond Pulses.- Chapter 3. Bright coherent XUV generation in microfluidic glass devices for ultrafast x-ray spectroscopy.- Chapter 4. Attosecond Physics and Quantum Information Science.- Chapter 5. Dynamics via Attosecond Four-Wave Mixing.- Chapter 6. Optical control of autoionizing states in argon.- Chapter 7. Retrieving a Complex Molecular Structure from Laser-Induced Electron Diffraction using Ma-chine Learning.- Chapter 8. Imaging ultrafast Dissociation Dynamics: OCS & Roaming in Formaldehyde.- Chapter 9. Controlling the time evolution of electron-nuclei entanglement for steering vibronic coherences dynamics induced by short 1-2 fs optical pulses.- Chapter 10. An MQDT model for the description of time resolved pump probe experiments.- Chapter 11. ASTRA, A Transition Density Matrix Approach to the Interaction of Attosecond Radiation with Atoms and Molecules.- Chapter 12. Symmetry-protected chiral sensitivity in photoionization with bichromatic fields.- Chapter 13. Experimental investigation of topological property of degenereate singularities in rescattering processes.- Chapter 14. Simulating strong field tunnel ionization of molecules.- Chapter 15. Control of photoelectron-ion entanglement in attosecond laser-induced photoionization of H2.- Chapter 16. Ultrafast Second-harmonic XUV Spectroscopy: A Novel Probe for Symmetry.- Chapter 17. From Ultrafast Light-Induced Currents to Spatially-Resolved Field Sampling.- Chapter 18. Attosecond core-exciton dynamics in wide-gap insulators.- Chapter 19. Polarization-Shaped Strong Field Control over Valley Polarization with Mid-IR Light.- Chapter 20. The Future of Attosecond Science.
Este título pertence ao(s) assunto(s) indicados(s). Para ver outros títulos clique no assunto desejado.