Temporal shaping of narrow-band picosecond pulses via non-colinear sum-frequency mixing of dispersion-controlled pulses

A long sought-after goal for photocathode electron sources has been to improve performance by temporally shaping the incident exitation laser pulse. The narrow bandwidth, short wavelength, and picosecond pulse duration make it challenging to employ conventional spectral pulse shaping techniques. We present a novel and efficient intensity-envelope shaping technique achieved during nonlinear upconversion through opposite-chirp sum-frequency mixing. We also present a numerical case-study of the LCLS-II photoinjector where transverse electron emittance is improved by at least 25%

Nonlinearly Shaped Pulses in Photoinjectors and Free-Electron Lasers

Photoinjectors and Free Electron Lasers (FEL) are amongst the most advanced systems in accelerator physics and have consistently pushed the boundaries of emittance and x-ray peak power. In this paper, laser shaping at the cathode is proposed to further lower the emittance and reduce electron beam tails, which would result in brighter x-ray production. Using dispersion controlled nonlinear shaping (DCNS), laser pulses and beam dynamics were simulated in LCLS-II. The photoinjector emittance was optimized and the resulting e-beam profiles were then simulated and optimized in the linac. Finally, the expected FEL performance is estimated and compared to the current technology: Gaussian laser pulses on the cathode. The e-beams produced by DCNS pulses show a potential for 35% increase in x-ray power per pulse during SASE when compared to the standard Gaussian laser pulses

Enhanced ultrafast X-ray diffraction by transient resonances

Diffraction-before-destruction imaging with single ultrashort X-ray pulses has the potential to visualise non-equilibrium processes, such as chemical reactions, at the nanoscale with sub-femtosecond resolution in the native environment without the need of crystallization. Here, a nanospecimen partially diffracts a single X-ray flash before sample damage occurs. The structural information of the sample can be reconstructed from the coherent X-ray interference image. State-of-art spatial resolution of such snapshots from individual heavy element nanoparticles is limited to a few nanometers. Further improvement of spatial resolution requires higher image brightness which is ultimately limited by bleaching effects of the sample. We compared snapshots from individual 100 nm Xe nanoparticles as a function of the X-ray pulse duration and incoming X-ray intensity in the vicinity of the Xe M-shell resonance. Surprisingly, images recorded with few femtosecond and sub-femtosecond pulses are up to 10 times brighter than the static linear model predicts. Our Monte-Carlo simulation and statistical analysis of the entire data set confirms these findings and attributes the effect to transient resonances. Our simulation suggests that ultrafast form factor changes during the exposure can increase the brightness of X-ray images by several orders of magnitude. Our study guides the way towards imaging with unprecedented combination of spatial and temporal resolution at the nanoscale