TY - JOUR
T1 - Electron-nuclear correlated multiphoton-route to Rydberg fragments of molecules
AU - Zhang, Wenbin
AU - Gong, Xiaochun
AU - Li, Hui
AU - Lu, Peifen
AU - Sun, Fenghao
AU - Ji, Qinying
AU - Lin, Kang
AU - Ma, Junyang
AU - Li, Hanxiao
AU - Qiang, Junjie
AU - He, Feng
AU - Wu, Jian
N1 - Publisher Copyright:
© 2019, The Author(s).
PY - 2019/12/1
Y1 - 2019/12/1
N2 - Atoms and molecules exposed to strong laser fields can be excited to the Rydberg states with very high principal quantum numbers and large orbitals. It allows acceleration of neutral particles, generate near-threshold harmonics, and reveal multiphoton Rabi oscillations and rich photoelectron spectra. However, the physical mechanism of Rydberg state excitation in strong laser fields is yet a puzzle. Here, we identify the electron-nuclear correlated multiphoton excitation as the general mechanism by coincidently measuring all charged and neutral fragments ejected from a H 2 molecule. Ruled by the ac-Stark effect, the internuclear separation for resonant multiphoton excitation varies with the laser intensity. It alters the photon energy partition between the ejected electrons and nuclei and thus leads to distinct kinetic energy spectra of the nuclear fragments. The electron-nuclear correlation offers an alternative visual angle to capture rich ultrafast processes of complex molecules.
AB - Atoms and molecules exposed to strong laser fields can be excited to the Rydberg states with very high principal quantum numbers and large orbitals. It allows acceleration of neutral particles, generate near-threshold harmonics, and reveal multiphoton Rabi oscillations and rich photoelectron spectra. However, the physical mechanism of Rydberg state excitation in strong laser fields is yet a puzzle. Here, we identify the electron-nuclear correlated multiphoton excitation as the general mechanism by coincidently measuring all charged and neutral fragments ejected from a H 2 molecule. Ruled by the ac-Stark effect, the internuclear separation for resonant multiphoton excitation varies with the laser intensity. It alters the photon energy partition between the ejected electrons and nuclei and thus leads to distinct kinetic energy spectra of the nuclear fragments. The electron-nuclear correlation offers an alternative visual angle to capture rich ultrafast processes of complex molecules.
UR - https://www.scopus.com/pages/publications/85061592114
U2 - 10.1038/s41467-019-08700-5
DO - 10.1038/s41467-019-08700-5
M3 - 文章
C2 - 30765696
AN - SCOPUS:85061592114
SN - 2041-1723
VL - 10
JO - Nature Communications
JF - Nature Communications
IS - 1
M1 - 757
ER -