TY - JOUR
T1 - Anion photoelectron velocity-map imaging using a tunable laser at a 100 kHz repetition rate
AU - Horio, Takuya
AU - Nishizato, Tasuku
AU - Suzuki, Yuta
AU - Matsumoto, Kazuaki
AU - Terasaki, Akira
N1 - Publisher Copyright:
© 2025 Author(s).
PY - 2025/1/14
Y1 - 2025/1/14
N2 - We present velocity-map imaging (VMI) of photoelectrons detached from anions using an optical parametric amplifier operating at a repetition rate as high as 100 kHz. The light source generates femtosecond (fs) laser pulses tunable from near-infrared to ultraviolet (310-2600 nm), which interact synchronously with mass-selected anion bunches. We demonstrate this technique by measuring two-dimensional projections of photoelectrons ejected from silver trimer anions, Ag3−, across a photon energy range from 2.43 to 4.00 eV (509-310 nm), with an average power of 50-300 mW. This high-repetition-rate VMI setup allows rapid data acquisition of photoelectron spectra and laboratory-frame photoelectron angular distributions of anions at various photon energies, facilitating investigation of their electronic and geometric structures. Taking advantage of the fs pulses, this approach will also enable time-resolved photoelectron imaging for tracking electronic and nuclear dynamics of anions with high efficiency.
AB - We present velocity-map imaging (VMI) of photoelectrons detached from anions using an optical parametric amplifier operating at a repetition rate as high as 100 kHz. The light source generates femtosecond (fs) laser pulses tunable from near-infrared to ultraviolet (310-2600 nm), which interact synchronously with mass-selected anion bunches. We demonstrate this technique by measuring two-dimensional projections of photoelectrons ejected from silver trimer anions, Ag3−, across a photon energy range from 2.43 to 4.00 eV (509-310 nm), with an average power of 50-300 mW. This high-repetition-rate VMI setup allows rapid data acquisition of photoelectron spectra and laboratory-frame photoelectron angular distributions of anions at various photon energies, facilitating investigation of their electronic and geometric structures. Taking advantage of the fs pulses, this approach will also enable time-resolved photoelectron imaging for tracking electronic and nuclear dynamics of anions with high efficiency.
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U2 - 10.1063/5.0245252
DO - 10.1063/5.0245252
M3 - Article
C2 - 39791496
AN - SCOPUS:85214920013
SN - 0021-9606
VL - 162
JO - Journal of Chemical Physics
JF - Journal of Chemical Physics
IS - 2
M1 - 026101
ER -