C. Hutchison

Femtosecond structural dynamics drives the trans/cis isomerization in photoactive yellow protein.

Visualizing a response to light Many biological processes depend on detecting and responding to light. The response is often mediated by a structural change in a protein that begins when absorption of a photon causes isomerization of a chromophore bound to the protein. Pande et al. used x-ray pulses emitted by a free electron laser source to conduct time-resolved serial femtosecond crystallography in the time range of 100 fs to 3 ms. This allowed for the real-time tracking of the trans-cis isomerization of the chromophore in photoactive yellow protein and the associated structural changes in the protein. Science, this issue p. 725 The trans-to-cis isomerization of a key chromophore is characterized on ultrafast time scales. A variety of organisms have evolved mechanisms to detect and respond to light, in which the response is mediated by protein structural changes after photon absorption. The initial step is often the photoisomerization of a conjugated chromophore. Isomerization occurs on ultrafast time scales and is substantially influenced by the chromophore environment. Here we identify structural changes associated with the earliest steps in the trans-to-cis isomerization of the chromophore in photoactive yellow protein. Femtosecond hard x-ray pulses emitted by the Linac Coherent Light Source were used to conduct time-resolved serial femtosecond crystallography on photoactive yellow protein microcrystals over a time range from 100 femtoseconds to 3 picoseconds to determine the structural dynamics of the photoisomerization reaction.

High-order harmonic generation in graphite plasma plumes using ultrashort laser pulses: a systematic analysis of harmonic radiation and plasma conditions

High-order harmonic generation in graphite-ablated plasmas was systematically studied using ultrashort (3.5 and 30 fs) laser pulses. We observed the efficient frequency conversion of 3.5 fs Ti:sapphire laser pulses in the range of 15-26 eV. Stabilization of the harmonic yield at a 1 kHz pulse repetition rate was accomplished using a rotating graphite target. We also show the results of harmonic generation in carbon plasma using 1300 nm, 40 ps pulses, which allowed the extension of the harmonic cutoff while maintaining a comparable conversion efficiency to the case of 780 nm driving radiation. The time-of-flight mass spectrometric analysis of the plasma components and the scanning electron microscopy of plasma debris under optimal conditions for harmonic generation suggest the presence of small carbon clusters (C10-C30 )i n the plasma plume at the moment of femtosecond pulse propagation, which further aggregate on nearby substrates. We present the results of plasma spectroscopy obtained under unoptimized plasma conditions that elucidate the reduction in harmonic signal. We also present calculations of plasma concentration under different excitation conditions of the ablated graphite target. (Some figures may appear in colour only in the online journal)

Stable generation of high-order harmonics of femtosecond laser radiation from laser produced plasma plumes at 1 kHz pulse repetition rate.

We present a method for the creation of stable weakly ionized plasmas from laser ablation of solid targets using a 1 kHz pulse repetition rate laser, which can be used for stable high-order harmonic generation from plasma plumes. The plasma plumes were generated from cylindrical rotating targets. Without target rotation the intensity of harmonics in the 40-80 nm range drops by more than one order of magnitude during less than 10(3) shots, while, with rotation of the target at typically 30 revolutions per minute, stable emission of high-order harmonics from aluminum plasma plumes with variation of less than 10% was maintained for >10(6) laser shots.

Enhancement of high harmonics from plasmas using two-color pump and chirp variation of 1 kHz Ti:sapphire laser pulses

We have investigated resonance effects in high-order harmonic generation (HHG) within laser-produced plasmas. We demonstrate a significantly improved harmonic yield by using two-color pump-induced enhancement and a 1 kHz pulse repetition rate. Together with an increased HHG output, the even harmonics in the cutoff region were enhanced with respect to odd harmonics. We report the observation of a resonance-induced growth in intensity of 20th harmonic in silver plasma (2×), 26th harmonic in vanadium plasma (4×), and 28th harmonic in chromium plasma (5×).

Isolated sub-fs XUV pulse generation in Mn plasma ablation

We report studies of high-order harmonic generation in laser-produced manganese plasmas using sub-4-fs drive laser pulses. The measured spectra exhibit resonant enhancement of a small spectral region of about 2.5 eV width around the 31st harmonic (~50eV). The intensity contrast relative to the directly adjacent harmonics exceeds one order of magnitude. This finding is in sharp contrast to the results reported previously for multi-cycle laser pulses [Physical Review A 76, 023831 (2007)]. Theoretical modelling suggests that the enhanced harmonic emission forms an isolated sub-femtosecond pulse.

Comparison of high-order harmonic generation in uracil and thymine ablation plumes

We present studies of high-order harmonic generation (HHG) in laser ablation plumes of the ribonucleic acid nucleobase uracil and its deoxyribonucleic acid counterpart thymine. Harmonics were generated using 780 nm, 30 fs and 1300 nm, 40 fs radiation upon ablation with 1064 nm, 10 ns or 780 nm, 160 ps pulses. Strong HHG signals were observed from uracil plumes with harmonics emitted with photon energies >55 eV. Results obtained in uracil plumes were compared with those from thymine, which did not yield signs of harmonic generation. The ablation plumes of the two compounds were examined by collection of the ablation debris on a silicon substrate placed in close proximity to the target and by time-of-flight mass spectrometry. From this evidence we conclude that the differences in HHG signal are due to the different fragmentation dynamics of the molecules in the plasma plume. These studies constitute the first attempt to analyse differences in structural properties of complex molecules through plasma ablation-induced HHG spectroscopy.

Spatial coherence measurements of non-resonant and resonant high harmonics generated in laser ablation plumes

We present measurements of the spatial coherence of the high-order harmonics generated in laser-produced ablation plumes. Harmonics were generated using 4 fs, 775 nm pulses with peak intensity 3 × 1014 W cm−2. Double-slit fringe visibilities in the range of ≈0.6–0.75 were measured for non-resonant harmonics in carbon and resonantly enhanced harmonics in zinc and indium. These are somewhat higher than the visibility obtained for harmonics generated in argon gas under similar conditions. This is attributed to lower time-dependent ionization of the plasma ablation targets compared to argon during the high harmonics generation process.

High-order harmonic generation from metal plasmas using 1 kHz laser pulses

High-order harmonic generation in laser-produced plasma was demonstrated on metal surfaces using a high pulse repetition rate laser (1 kHz). It was found that if sufficiently thick bulk targets were used thermal conduction was sufficient to prevent any deterioration in the metal plasma plume production at this repetition rate. Under appropriate conditions harmonic yields were found to remain stable for >105 laser shots without the need to move the target. The high repetition rate allowed both short and long electron trajectories to be clearly identified during harmonic generation from the metal plasmas.

Molecular internal dynamics studied by quantum path interferences in high order harmonic generation

Abstract We investigate how short and long electron trajectory contributions to high harmonic emission and their interferences give access to information about intra-molecular dynamics. In the case of unaligned molecules, we show experimental evidence that the long trajectory contribution is more dependent upon the molecular species than the short one, providing a high sensitivity to cation nuclear dynamics from 100’s of as to a few fs after ionisation. Using theoretical approaches based on the strong field approximation and numerical integration of the time dependent Schrodinger equation, we examine how quantum path interferences encode electronic motion when the molecules are aligned. We show that the interferences are dependent upon which ionisation channels are involved and any superposition between them. In particular, quantum path interferences can encode signatures of electron dynamics if the laser field drives a coupling between the channels. Hence, molecular quantum path interferences are a promising method for attosecond spectroscopy, allowing the resolution of ultra-fast charge migration in molecules after ionisation in a self-referenced manner.

Electron trajectory control of odd and even order harmonics in high harmonic generation using an orthogonally polarised second harmonic field

We investigate quantum trajectory control in high-order harmonic generation using an additional orthogonally polarised second harmonic field. By controlling the relative phase between this field and the fundamental, we are able to suppress and enhance particular electron trajectories which results in a modulation of the harmonic emission. We observe a phase shift of the modulation between the short and long trajectories that is different for adjacent odd and even harmonics. These results show qualitative agreement with a full propagation calculation where the single atom response was obtained from the strong field approximation and the main results are explained by consideration of a single atom quantum orbit picture.