We apply ultrafast pump-push-photocurrent and pump-push-photoluminescence spectroscopies to polyfluorene organic diode to track in time the bound exciton formation. ‘Cold’-excitons become bound within 10-fs while ‘hot’-excitons can dissociate spontaneously within 50-fs before acquiring bound character.

Fundamental mechanisms underlying exciton formation in organic semiconductors are complex and elusive as it occurs on ultrashort sub-100-fs timescales. Some fundamental aspects of this process, such as the evolution of exciton binding energy, have not been resolved in time experimentally. Here, we apply a combination of sub-10-fs Pump-Push-Photocurrent, Pump-Push-Photoluminescence, and Pump-Probe spectroscopies to polyfluorene devices to track the ultrafast formation of excitons. While Pump-Probe is sensitive to the total concentration of excited states, Pump-Push-Photocurrent and Pump-Push-Photoluminescence are sensitive to bound states only, providing access to exciton binding dynamics. We find that excitons created by near-absorption-edge photons are intrinsically bound states, or become such within 10 fs after excitation. Meanwhile, excitons with a modest >0.3 eV excess energy can dissociate spontaneously within 50 fs before acquiring bound character. These conclusions are supported by excited-state molecular dynamics simulations and a global kinetic model which quantitatively reproduce experimental data.

The possibility of suddenly ionized molecules undergoing extremely fast electron hole dynamics prior to significant structural change was first recognized more than 20 years ago and termed charge migration. The accurate probing of ultrafast electron hole dynamics requires measurements that have both sufficient temporal resolution and can detect the localization of a specific hole within the molecule. We report an investigation of the dynamics of inner valence hole states in isopropanol where we use an x-ray pump/x-ray probe experiment, with site and state-specific probing of a transient hole state localized near the oxygen atom in the molecule, together with an ab initio theoretical treatment. We record the signature of transient hole dynamics and make the first observation of dynamics driven by frustrated Auger-Meitner transitions. We verify that the hole lifetime is consistent with our theoretical prediction. This state-specific measurement paves the way to widespread application for observations of transient hole dynamics localized in space and time in molecules and thus to charge transfer phenomena that are fundamental in chemical and material physics.

Here, using single-material OPV device and laser system with sub-10fs time resolution, we track in time the formation of localised excitonic states. For this we employ a combination of pump-probe (PP) spectroscopy, sensitive to concentration of excited states, and pump-push-photocurrent (PPPC) technique, sensitive to the state localisation. Combining both methods to monitor charge dynamics at real operation condition allows to separate and track the evolution of strongly bound and spontaneously dissociating excited states. Our data show that PP and PPPC measurement do not follow the same trend, and the discrepancy between the states probed by PP and PPPC indicates that excitons acquire localised character within first 50fs after formation. Results may be useful for a new realisation of efficient donor-acceptor OPV design.

We have generated isolated attosecond pulses and performed attosecond streaking measurements using a two-colour synthesized laser field consisting of a strong near-infrared few-cycle pulse and a weaker multi-cycle pulse centred at 400 nm. An actively stabilized interferometer was used to coherently combine the two pulses. Using attosecond streaking we characterised the electric fields of the two pulses and accurately retrieved the spectrum of the multi-cycle pulse. We demonstrated a two-fold increase in the flux of isolated attosecond pulses produced and show that their duration was minimally affected by the presence of the weaker field due to spectral filtering by a multilayer mirror.

High-harmonic radiation in the extreme ultraviolet and soft X-ray spectral regions can be used to generate attosecond pulses and to obtain structural and dynamic information in atoms and molecules. However, these sources typically suffer from a limited photon flux. An additional issue at lower photon energies is the appearance of satellites in the time domain, stemming from insufficient temporal gating and the spectral filtering required for the isolation of attosecond pulses. Such satellites limit the temporal resolution. The use of multi-colour driving fields has been proven to enhance the harmonic yield and provide additional control, using the relative delays between the different spectral components for waveform shaping. We describe here a two-colour high-harmonic source that combines a few-cycle near-infrared pulse with a multi-cycle second harmonic pulse, with both relative phase and carrier-envelope phase stabilization. We observe strong modulations in the harmonic flux, and present simulations and experimental results supporting the suppression of satellites in sub-femtosecond pulses at 20 eV compared to the single colour field case, an important requirement for attosecond pump-probe measurements.

Recent studies confirmed that the materials used in the extreme UV and soft X-ray regime for precise characterization of intense free-electron laser pulses (e.g., Si3N4) do not work efficiently in the hard X-ray regime, which is due to the fact that the impact of a hard X-ray photon is followed by a series of electron cascading processes. Following theoretical indication, we show that this limitation can be circumvented and the cascading time can be significantly reduced if the X-ray photon energy is double the ionization energy. We investigate an alternative material for pulse diagnostics, SnO2, using the Linac Coherent Light Source at photon energies of 5 keV and 9 keV. We prove the validity of the concept and show that it has a large potential for practical applications. By applying the proposed criteria, the temporal accuracy of the non-invasive pulse diagnostic tools can be improved in current and emerging hard X-ray facilities.

We have studied high-order harmonic generation (HHG) in an indium ablation plume driven by intense few-cycle laser pulses centered at 775 nm as a function of the frequency chirp of the laser pulse. We found experimentally that resonant emission lines between 19.7 eV and 22.3 eV (close to the 13th and 15th harmonic of the laser) exhibit a strong, asymmetric chirp dependence, with pronounced intensity modulations. The chirp dependence is reproduced by our numerical time-dependent Schrödinger equation simulations of a resonant HHG by the model indium ion. As demonstrated with our separate simulations of HHG within the strong field approximation, the resonance can be understood in terms of the chirp-dependent HHG photon energy coinciding with the energy of an autoionizing state to ground state transition with high oscillator strength. This supports the validity of the general theory of resonant four-step HHG in the few-cycle limit.

Pulse characterization technology to characterize space-time couplings exists but most technqiues are not suiatable for few-cycle pulses. A lot of recent work has been focussed on combining modern few-cycle pulse characterization methods with spatial phase measurements based on a filtered reference pulse.This work reviews current state of the art in this field and also show recent results and progress in the self-referenced characterization of near single cycle pulses with space-time couplings. Using SEA-F-SPIDER the spatio-temporal electric field of a laser pulse can be reconstructed without the need for a reference pulse. In the current implementation we can recover the field E(x,t) in one spatial dimension. Measurements of ultrafast wavefront rotation and pulse front tilt in pulses generated in hollow fiber compressors are presented. The paper also discusses application in OPCPA and NOPA systems where the amplified pulses are expected to carry a significant amount of space-time couplings. Furthermore, avenues towards the extension of the technique to both spatial dimensions for a complete reconstruction of E(x,y,t) are discussed.

Non-linear photoionization of molecules in the 10-50 eV range is a prerequisite for pump-probe measurements with sub-femtosecond resolution, but hitherto has been limited to femtosecond resolution, low repetition rate and high photon flux laser systems. We demonstrate two-photon single ionization of helium atoms using 100 pJ, 1.34 fs pulses (main peak FWHM = 680 as) at 1 kHz repetition rate with a central photon energy of 19.6 eV. We obtained an exponent of 2.27 +/- 0.21 for the intensity dependence of the signal and a two-photon ionization cross-section of 5.0 +/- 0.5 x 10(-50) cm(4) s. Our work opens the possibility of attosecond pump-probe measurements of ultrafast molecular processes. (C) 2017 Published by Elsevier B.V.

Free-electron lasers providing ultra-short high-brightness pulses of X-ray radiation have great potential for a wide impact on science, and are a critical element for unravelling the structural dynamics of matter. To fully harness this potential, we must accurately know the X-ray properties: intensity, spectrum and temporal profile. Owing to the inherent fluctuations in free-electron lasers, this mandates a full characterization of the properties for each and every pulse. While diagnostics of these properties exist, they are often invasive and many cannot operate at a high-repetition rate. Here, we present a technique for circumventing this limitation. Employing a machine learning strategy, we can accurately predict X-ray properties for every shot using only parameters that are easily recorded at high-repetition rate, by training a model on a small set of fully diagnosed pulses. This opens the door to fully realizing the promise of next-generation high-repetition rate X-ray lasers.

We show the application of time-domain ptychography for the self-referenced characterization of near single-cycle laser pulses. Using spatial multiplexing spatio-temporal pulse characterization is demonstrated.

We report, to the best of our knowledge, the first application of time-domain ptychography for the characterization of few-cycle laser pulses. Our method enables zero-additional phase measurements of over-octave-spanning laser pulses in the single cycle regime. The spectral phase is recovered using a robust ptychography algorithm that requires no input apart from the measured data trace. In addition to numerical tests, we validate our new device experimentally by reconstructing the complex electric field of a 1.5 cycle laser pulse with a bandwidth spanning 490 to 1060 nm. We further check the accuracy of our device by comparing the measured phases of octave-spanning chirped pulses to the known dispersion of fused silica glass.

We report on the characterization of space-time couplings in high-energy sub-2-cycle 770 nm laser pulses using a self-referencing single-frame method. Using spatially encoded arrangement filter-based spectral phase interferometry for direct electric field reconstruction, we characterize few-cycle pulses with a wavefront rotation of 2.8×1011  rev/s (1.38 mrad per half-cycle) and pulses with pulse front tilts ranging from -0.33  fs/μm to -3.03  fs/μm in the focus.

We report the first measurement of the near oxygen K-edge auger spectrum of the glycine molecule. Our work employed an x-ray free electron laser as the photon source operated with input photon energies tunable between 527 and 547 eV. Complete electron spectra were recorded at each photon energy in the tuning range, revealing resonant and non-resonant auger structures. Finally ab initio theoretical predictions are compared with the measured above the edge auger spectrum and an assignment of auger decay channels is performed.

Rapid proton migration is a key process in hydrocarbon photochemistry. Charge migration and subsequent proton motion can mitigate radiation damage when heavier atoms absorb X-rays. If rapid enough, this can improve the fidelity of diffract-before-destroy measurements of biomolecular structure at X-ray-free electron lasers. Here we study X-ray-initiated isomerization of acetylene, a model for proton dynamics in hydrocarbons. Our time-resolved measurements capture the transient motion of protons following X-ray ionization of carbon K-shell electrons. We Coulomb-explode the molecule with a second precisely delayed X-ray pulse and then record all the fragment momenta. These snapshots at different delays are combined into a 'molecular movie' of the evolving molecule, which shows substantial proton redistribution within the first 12 fs. We conclude that significant proton motion occurs on a timescale comparable to the Auger relaxation that refills the K-shell vacancy.

Researchers have synchronized XUV and VUV attosecond pulses simultaneously generated by high-harmonic generation. Such pulses with different photon energies may be useful for pump–probe experiments. The development of attosecond pulses across different photon energies is an essential precursor to performing pump–probe attosecond experiments in complex systems, where the potential of attosecond science1 can be further developed2,3. We report the generation and characterization of synchronized extreme ultraviolet (90 eV) and vacuum ultraviolet (20 eV) pulses, generated simultaneously via high-harmonic generation. The vacuum ultraviolet pulses are well suited for pump–probe experiments that exploit the high photo-ionization cross-sections of many molecules in this spectral region4 as well as the higher photon flux due to the higher conversion efficiency of the high harmonic generation process at these energies5. We temporally characterized all pulses using the attosecond streaking technique6 and the FROG-CRAB retrieval method7. We report 576 ± 16 as pulses at 20 eV and 257 ± 21 as pulses at 90 eV. Our demonstration of synchronized attosecond pulses at different photon energies, which are inherently jitter-free due to the common-path geometry implemented, offers unprecedented possibilities for pump–probe studies.

Synchronised pulses generated at 20 eV and 90 eV for attosecond pump probe experiments D. Fabris, T. Witting, W. A. Okell, D. J. Walke, P. Matia-Hernando, J. Henkel, T. R. Barillot, M. Lein, J. P. Marangos, J. W. G. Tisch 1 Blackett Laboratory, Imperial College, London SW7 2AZ, UK 2 Institut für Theoretische Physik and Centre for Quantum Engineering and Space-Time Research, Leibniz Universität Hannover, Appelstraße 2, D-30167 Hannover, Germany Corresponding author: d.fabris11@imperial.ac.uk