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Register a new userSelf-referenced coherent diffraction x-ray movie of Angstrom- and femtosecond-scale atomic motion
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Time-resolved femtosecond x-ray diffraction patterns from laser-excited molecular iodine are used to create a movie of intramolecular motion with time and space resolution of $30~$fs and $0.3$ AA . The high spatial fidelity is due to interference between the moving excitation and the static initial charge distribution. This x-ray interference has not been employed to image internal motion in molecules before. The initial state is used as the local oscillator for heterodyne amplification of the excited charge distribution to retrieve real-space movies of atomic motion on AA ngstrom and femtosecond scales. Coherent vibrational motion and dispersion, dissociation, and rotational dephasing are all clearly visible in the data, thereby demonstrating the stunning sensitivity of heterodyne methods.
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The capability of generating two intense, femtosecond x-ray pulses with controlled time delay opens the possibility of performing time-resolved experiments for x-ray induced phenomena. We have applied this capability to study the photoinduced dynamics in diatomic molecules. In molecules composed of low-Z elements, textit{K}-shell ionization creates a core-hole state in which the main decay mode is an Auger process involving two electrons in the valence shell. After Auger decay, the nuclear wavepackets of the transient two-valence-hole states continue evolving on the femtosecond timescale, leading either to separated atomic ions or long-lived quasi-bound states. By using an x-ray pump and an x-ray probe pulse tuned above the textit{K}-shell ionization threshold of the nitrogen molecule, we are able to observe ion dissociation in progress by measuring the time-dependent kinetic energy releases of different breakup channels. We simulated the measurements on N$_2$ with a molecular dynamics model that accounts for textit{K}-shell ionization, Auger decay, and the time evolution of the nuclear wavepackets. In addition to explaining the time-dependent feature in the measured kinetic energy release distributions from the dissociative states, the simulation also reveals the contributions of quasi-bound states.
We demonstrate how to use feedback to control the internal states of trapped coherent ensembles of two-level atoms, and to protect a superposition state against the decoherence induced by a collective noise. Our feedback scheme is based on weak optical measurements with negligible back-action and coherent microwave manipulations. The efficiency of the feedback system is studied for a simple binary noise model and characterized in terms of the trade-off between information retrieval and destructivity from the optical probe. We also demonstrate the correction of more general types of collective noise. This technique can be used for the operation of atomic interferometers beyond the standard Ramsey scheme, opening the way towards improved atomic sensors.
Atoms trapped in the evanescent field around a nanofiber experience strong coupling to the light guided in the fiber mode. However, due to the intrinsically strong positional dependence of the coupling, thermal motion of the ensemble limits the use of nanofiber trapped atoms for some quantum tasks. We investigate the thermal dynamics of such an ensemble by using short light pulses to make a spatially inhomogeneous population transfer between atomic states. As we monitor the wave packet of atoms created by this scheme, we find a damped oscillatory behavior which we attribute to sloshing and dispersion of the atoms. Oscillation frequencies range around 100 kHz, and motional dephasing between atoms happens on a timescale of 10 $mu$s. Comparison to Monte Carlo simulations of an ensemble of 1000 classical particles yields reasonable agreement for simulated ensemble temperatures between 25 $mu$K and 40 $mu$K.
Short wavelength Free-Electron Lasers (FELs) are the newest light sources available to scientists to probe a wide range of phenomena, with chemical, physical and biological applications, using soft and hard X-rays. These sources include the currently most powerful light sources in the world (hard X-ray sources) and are characterised by extremely high powers and high transverse coherence, but the first FELs had reduced longitudinal coherence. Now it is possible to achieve good longitudinal coherence (narrow bandwidth in the frequency domain) and here we discuss and illustrate a range of experiments utilising this property, and their underlying physics. The primary applications are those which require high resolution (for example resonant experiments), or temporal coherence (for example coherent control experiments). The currently available light sources extend the vast range of laboratory laser techniques to short wavelengths.
The counting and control of optical cycles of light has become common with modelocked laser frequency combs. But even with advances in laser technology, modelocked laser combs remain bulk-component devices that are hand-assembled. In contrast, a frequency comb based on the Kerr-nonlinearity in a dielectric microresonator will enable frequency comb functionality in a micro-fabricated and chip-integrated package suitable for use in a wide-range of environments. Such an advance will significantly impact fields ranging from spectroscopy and trace gas sensing, to astronomy, communications, atomic time keeping and photonic data processing. Yet in spite of the remarkable progress shown over the past years, microresonator frequency combs (microcombs) have still been without the key function of direct f-2f self-referencing and phase-coherent frequency control that will be critical for enabling their full potential. Here we realize these missing elements using a low-noise 16.4 GHz silicon chip microcomb that is coherently broadened from its initial 1550 nm wavelength and subsequently f-2f self-referenced and phase-stabilized to an atomic clock. With this advance, we not only realize the highest repetition rate octave-span frequency comb ever achieved, but we highlight the low-noise microcomb properties that support highest atomic clock limited frequency stability.
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