Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Valentina Utrio Lanfaloni"'
Autor:
Kristina S. Zinchenko, Fernando Ardana-Lamas, Valentina Utrio Lanfaloni, Nicholas Monahan, Issaka Seidu, Michael S. Schuurman, Simon P. Neville, Hans Jakob Wörner
Publikováno v:
Structural Dynamics, Vol 10, Iss 6, Pp 064303-064303-13 (2023)
The Jahn–Teller effect (JTE) is central to the understanding of the physical and chemical properties of a broad variety of molecules and materials. Whereas the manifestations of the JTE in stationary properties of matter are relatively well studied
Externí odkaz:
https://doaj.org/article/06812ff2290b4d71b0f0f245f35e492e
Autor:
Kristina S. Zinchenko, Fernando Ardana-Lamas, Valentina Utrio Lanfaloni, Tran Trung Luu, Yoann Pertot, Martin Huppert, Hans Jakob Wörner
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-10 (2023)
Abstract We present an apparatus for attosecond transient-absorption spectroscopy (ATAS) featuring soft-X-ray (SXR) supercontinua that extend beyond 450 eV. This instrument combines an attosecond table-top high-harmonic light source with mid-infrared
Externí odkaz:
https://doaj.org/article/c8cb5aa4d0d9439983244b10795b24ed
Autor:
Valentina Utrio Lanfaloni, Kristina S. Zinchenko, Fernando Ardana-Lamas, Nicholas Monahan, Issaka Seidu, Simon P. Neville, Joscelyn van der Veen, Michael S. Schuurman, Hans Jakob Wörner
We demonstrate attosecond transient-absorption spectroscopy (ATAS) at the carbon K-edge as a powerful technique to detect few-femtosecond electronic dynamics driven by conical intersections in gas-phase organic molecules, revealing the fastest electr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::902298d8724c8a9aa374f5f84ec80cb9
https://doi.org/10.1364/up.2022.w2b.5
https://doi.org/10.1364/up.2022.w2b.5
Autor:
F. Ardana-Lamas, Simon P. Neville, Joscelyn van der Veen, Michael S. Schuurman, Issaka Seidu, Kristina Zinchenko, Valentina Utrio Lanfaloni, Hans Jakob Wörner
Publikováno v:
Science
Science, 371 (6528)
Science, 371 (6528)
Conical intersections allow electronically excited molecules to return to their electronic ground state. Here, we observe the fastest electronic relaxation dynamics measured to date by extending attosecond transient-absorption spectroscopy (ATAS) to