scholarly journals In situ characterization of few-cycle laser pulses in transient absorption spectroscopy

2015 ◽  
Vol 40 (15) ◽  
pp. 3464 ◽  
Author(s):  
Alexander Blättermann ◽  
Christian Ott ◽  
Andreas Kaldun ◽  
Thomas Ding ◽  
Veit Stooß ◽  
...  
2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Thomas Ding ◽  
Marc Rebholz ◽  
Lennart Aufleger ◽  
Maximilian Hartmann ◽  
Veit Stooß ◽  
...  

AbstractHigh-intensity ultrashort pulses at extreme ultraviolet (XUV) and x-ray photon energies, delivered by state-of-the-art free-electron lasers (FELs), are revolutionizing the field of ultrafast spectroscopy. For crossing the next frontiers of research, precise, reliable and practical photonic tools for the spectro-temporal characterization of the pulses are becoming steadily more important. Here, we experimentally demonstrate a technique for the direct measurement of the frequency chirp of extreme-ultraviolet free-electron laser pulses based on fundamental nonlinear optics. It is implemented in XUV-only pump-probe transient-absorption geometry and provides in-situ information on the time-energy structure of FEL pulses. Using a rate-equation model for the time-dependent absorbance changes of an ionized neon target, we show how the frequency chirp can be directly extracted and quantified from measured data. Since the method does not rely on an additional external field, we expect a widespread implementation at FELs benefiting multiple science fields by in-situ on-target measurement and optimization of FEL-pulse properties.


1991 ◽  
Vol 11 (2) ◽  
pp. 83-93 ◽  
Author(s):  
G. Siuzdak ◽  
J. J. Belbruno

The phenoxy cation has been generated in polar and nonpolar solutions by multiphoton ionization of nitrobenzene using nanosecond pulses of 266 nm and 355 nm light. The ions have been characterized by pulsed conductivity (ion mobility) measurements and transient absorption spectroscopy. The involvement of the phenoxy ion in ion-molecule chemistry with either neutral solute or solvent molecules has also been observed and the photochemical products and quantum yields of the ion-molecule products are presented and compared with the neutral photochemistry results.


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