Observing electron localization in a dissociating H2+ molecule in real time.

Dissociation of diatomic molecules with odd number of electrons always causes the unpaired electron to localize on one of the two resulting atomic fragments. In the simplest diatomic molecule H2+ dissociation yields a hydrogen atom and a proton with the sole electron ending up on one of the two nuclei. That is equivalent to breaking of a chemical bond-the most fundamental chemical process. Here we observe such electron localization in real time by performing a pump-probe experiment. We demonstrate that in H2+ electron localization is complete in just 15 fs when the molecule's internuclear distance reaches 8 atomic units. The measurement is supported by a theoretical simulation based on numerical solution of the time-dependent Schrödinger equation. This observation advances our understanding of detailed dynamics of molecular dissociation.

Isotope Effect in Tunneling Ionization of Neutral Hydrogen Molecules.

It has been recently predicted theoretically that due to nuclear motion light and heavy hydrogen molecules exposed to strong electric field should exhibit substantially different tunneling ionization rates [O. I. Tolstikhin, H. J. Worner, and T. Morishita, Phys. Rev. A 87, 041401(R) (2013)]. We studied that isotope effect experimentally by measuring relative ionization yields for each species in a mixed H_{2}/D_{2} gas jet interacting with intense femtosecond laser pulses. In a reaction microscope apparatus, we detected ionic fragments from all contributing channels (single ionization, dissociation, and sequential double ionization) and determined the ratio of total single ionization yields for H_{2} and D_{2}. The measured ratio agrees quantitatively with the prediction of the generalized weak-field asymptotic theory in an apparent failure of the frozen-nuclei approximation.

The interaction of excited atoms and few-cycle laser pulses.

This work describes the first observations of the ionisation of neon in a metastable atomic state utilising a strong-field, few-cycle light pulse. We compare the observations to theoretical predictions based on the Ammosov-Delone-Krainov (ADK) theory and a solution to the time-dependent Schrödinger equation (TDSE). The TDSE provides better agreement with the experimental data than the ADK theory. We optically pump the target atomic species and measure the ionisation rate as the a function of different steady-state populations in the fine structure of the target state which shows significant ionisation rate dependence on populations of spin-polarised states. The physical mechanism for this effect is unknown.

Precise and Accurate Measurements of Strong-Field Photoionization and a Transferable Laser Intensity Calibration Standard.

Ionization of atoms and molecules in strong laser fields is a fundamental process in many fields of research, especially in the emerging field of attosecond science. So far, demonstrably accurate data have only been acquired for atomic hydrogen (H), a species that is accessible to few investigators. Here, we present measurements of the ionization yield for argon, krypton, and xenon with percent-level accuracy, calibrated using H, in a laser regime widely used in attosecond science. We derive a transferable calibration standard for laser peak intensity, accurate to 1.3%, that is based on a simple reference curve. In addition, our measurements provide a much needed benchmark for testing models of ionization in noble-gas atoms, such as the widely employed single-active electron approximation.

Transverse electron momentum distribution in tunneling and over the barrier ionization by laser pulses with varying ellipticity.

We study transverse electron momentum distribution in strong field atomic ionization driven by laser pulses with varying ellipticity. We show, both experimentally and theoretically, that the transverse electron momentum distribution in the tunneling and over the barrier ionization regimes evolves in a qualitatively different way when the ellipticity parameter describing polarization state of the driving laser pulse increases.

Experimental observation of the elusive double-peak structure in R-dependent strong-field ionization rate of H2(+).

When a diatomic molecule is ionized by an intense laser field, the ionization rate depends very strongly on the inter-nuclear separation. That dependence exhibits a pronounced maximum at the inter-nuclear separation known as the "critical distance". This phenomenon was first demonstrated theoretically in H2(+) and became known as "charge-resonance enhanced ionization" (CREI, in reference to a proposed physical mechanism) or simply "enhanced ionization"(EI). All theoretical models of this phenomenon predict a double-peak structure in the R-dependent ionization rate of H2(+). However, such double-peak structure has never been observed experimentally. It was even suggested that it is impossible to observe due to fast motion of the nuclear wavepackets. Here we report a few-cycle pump-probe experiment which clearly resolves that elusive double-peak structure. In the experiment, an expanding H2(+) ion produced by an intense pump pulse is probed by a much weaker probe pulse. The predicted double-peak structure is clearly seen in delay-dependent kinetic energy spectra of protons when pump and probe pulses are polarized parallel to each other. No structure is seen when the probe is polarized perpendicular to the pump.

Picosecond 554 nm yellow-green fiber laser source with average power over 1 W.

We demonstrate a source of 554 nm pulses with 2.7 ps pulse duration and 1.41 W average power, at a repetition rate of 300 MHz. The yellow-green pulse train is generated from the second harmonic of a 1.11 µm fiber laser source in periodically-poled stoichiometric LiTaO3. A total fundamental power of 2.52 W was used, giving a conversion efficiency of 56%.

Detection-enhanced steady state entanglement with ions.

Driven dissipative steady state entanglement schemes take advantage of coupling to the environment to robustly prepare highly entangled states. We present a scheme for two trapped ions to generate a maximally entangled steady state with fidelity above 0.99, appropriate for use in quantum protocols. Furthermore, we extend the scheme by introducing detection of our dissipation process, significantly enhancing the fidelity. Our scheme is robust to anomalous heating and requires no sympathetic cooling.

Controllable optical phase shift over one radian from a single isolated atom.

Fundamental optics such as lenses and prisms work by applying phase shifts of several radians to incoming light, and rapid control of such phase shifts is crucial to telecommunications. However, large, controllable optical phase shifts have remained elusive for isolated quantum systems. We have used a single trapped atomic ion to induce and measure a large optical phase shift of 1.3±0.1 radians in light scattered by the atom. Spatial interferometry between the scattered light and unscattered illumination light enables us to isolate the phase shift in the scattered component. The phase shift achieves the maximum value allowed by atomic theory over the accessible range of laser frequencies, pointing out new opportunities in microscopy and nanophotonics. Single-atom phase shifts of this magnitude open up new quantum information protocols, in particular long-range quantum phase-shift-keying cryptography.

Quantum interface between an electrical circuit and a single atom.

We show how to bridge the divide between atomic systems and electronic devices by engineering a coupling between the motion of a single ion and the quantized electric field of a resonant circuit. Our method can be used to couple the internal state of an ion to the quantized circuit with the same speed as the internal-state coupling between two ions. All the well-known quantum information protocols linking ion internal and motional states can be converted to protocols between circuit photons and ion internal states. Our results enable quantum interfaces between solid state qubits, atomic qubits, and light, and lay the groundwork for a direct quantum connection between electrical and atomic metrology standards.

Phase-coherent repetition rate multiplication of a mode-locked laser from 40 MHz to 1 GHz by injection locking.

We have used injection locking to multiply the repetition rate of a passively mode-locked femtosecond fiber laser from 40 MHz to 1 GHz while preserving optical phase coherence between the master laser and the slave output. The system is implemented almost completely in fiber and incorporates gain and passive saturable absorption. The slave repetition rate is set to a rational harmonic of the master repetition rate, inducing pulse formation at the least common multiple of the master and slave repetition rates.

Extreme ultraviolet interferometer using high-order harmonic generation from successive sources.

We present a new interferometer technique whereby multiple extreme ultraviolet light pulses are generated at different positions within a single laser focus (i.e., from successive sources) with a highly controllable time delay. The interferometer technique is tested with two generating media to create two extreme ultraviolet light pulses with a time delay between them. The delay is found to be a consequence of the Gouy phase shift. Ultimately the apparatus is capable of accessing unprecedented time scales by allowing stable and repeatable delays as small as 100 zs.

Experimental ionization of atomic hydrogen with few-cycle pulses.

We present experimental data on strong-field ionization of atomic hydrogen by few-cycle laser pulses. We obtain quantitative agreement at the 10% level between the data and an ab initio simulation over a wide range of laser intensities and electron energies.

Quantum optical waveform conversion.

Proposals for long-distance quantum communication rely on the entanglement of matter-based quantum nodes through optical communications channels, but the entangling light pulses have poor temporal behavior in current experiments. Here we show that nonlinear mixing of a quantum light pulse with a spectrally tailored classical field can compress the quantum pulse by more than a factor of 100 and flexibly reshape its temporal waveform while preserving all quantum properties, including entanglement. Our scheme paves the way for quantum communication at the full data rate of optical telecommunications.

Wavelength-scale imaging of trapped ions using a phase Fresnel lens.

A microfabricated phase Fresnel lens was used to image ytterbium ions trapped in a radio frequency Paul trap. The ions were laser cooled close to the Doppler limit on the 369.5 nm transition, reducing the ion motion so that each ion formed a near point source. By detecting the ion fluorescence on the same transition, near-diffraction-limited imaging with spot sizes of below 440 nm (FWHM) was achieved. To our knowledge, this is the first demonstration of wavelength-scale imaging of trapped ions and the highest imaging resolution ever achieved with atoms in free space.

Self-focusing in air with phase-stabilized few-cycle light pulses.

We investigate the nonlinear optical phenomenon of self-focusing in air with phase-stabilized few-cycle light pulses. This investigation looks at the role of the carrier-envelope phase by observing a filament in air, a nonlinear phenomenon that can be utilized for few-cycle pulse compression [Appl. Phys. B79, 673 (2004)]. We were able to measure the critical power for self-focusing in air to be 18+/-1 GW for a 6.3 fs pulse centered at 800 nm. Using this value and a basic first-order theory, we predicted that the self-focusing distance should deviate by 790 mum as the carrier-envelope phase is shifted from 0 to pi/2 rad. In contrast, the experimental results showed no deviation in the focus distance with a 3sigma upper limit of 180 mum. These counterintuitive results show the need for further study of self-focusing dynamics in the few-cycle regime.

Mode-locked picosecond pulse generation from an octave-spanning supercontinuum.

We generate mode-locked picosecond pulses near 1110 nm by spectrally slicing and reamplifying an octave-spanning supercontinuum source pumped at 1550 nm. The 1110 nm pulses are near transform-limited, with 1.7 ps duration over their 1.2 nm bandwidth, and exhibit high interpulse coherence. Both the supercontinuum source and the pulse synthesis system are implemented completely in fiber. The versatile source construction suggests that pulse synthesis from sliced supercontinuum may be a useful technique across the 1000 - 2000 nm wavelength range.

An automated submicron beam profiler for characterization of high numerical aperture optics.

An automated, interferometrically referenced scanning knife-edge beam profiler with submicron resolution is demonstrated by directly measuring the focusing properties of three aspheric lenses with numerical aperture (NA) between 0.53 and 0.68, with spatial resolution of 0.02 microm. The results obtained for two of the three lenses tested were in agreement with paraxial Gaussian beam theory. It was also found that the highest NA aspheric lens, which was designed for 830 nm, was not diffraction limited at 633 nm. This process was automated using motorized translation stages and provides a direct method for testing the design specifications of high numerical aperture optics.

Laser cooling of trapped ytterbium ions with an ultraviolet diode laser.

We demonstrate an ultraviolet diode laser system for cooling of trapped ytterbium ions. The laser power and linewidth are comparable to those of previous systems based on resonant frequency doubling, but the system is simpler, more robust, and less expensive. We use the laser system to cool small numbers of ytterbium ions confined in a linear Paul trap. From the observed spectra, we deduce final temperatures of < 270 mK.

Automatic feedback control of an Er-doped fiber laser with an intracavity loss modulator.

Suppression of Q-switching instabilities with an actively controlled intracavity loss modulator is demonstrated in an Er-doped waveguide laser that is mode locked with a slow saturable absorber at repetition rates of as much as 100 MHz. By automatic gain control in the feedback loop, stable mode locking is achieved over the entire parameter range of the laser. This approach renders laser stabilization independent of the characteristics of the gain medium and intracavity power. The pulse-shaping dynamics is not affected by the presence of the intracavity loss modulator.