Isolated single-cycle attosecond pulses

We generated single-cycle isolated attosecond pulses around approximately 36 electron volts using phase-stabilized 5-femtosecond driving pulses with a modulated polarization state. Using a complete temporal characterization technique, we demonstrated the compression of the generated pulses for as low as 130 attoseconds, corresponding to less than 1.2 optical cycles. Numerical simulations of the generation process show that the carrier-envelope phase of the attosecond pulses is stable. The availability of single-cycle isolated attosecond pulses opens the way to a new regime in ultrafast physics, in which the strong-field electron dynamics in atoms and molecules is driven by the electric field of the attosecond pulses rather than by their intensity profile.     

Observation of a train of attosecond pulses from high harmonic generation

In principle, the temporal beating of superposed high harmonics obtained by focusing a femtosecond laser pulse in a gas jet can produce a train of very short intensity spikes, depending on the relative phases of the harmonics. We present a method to measure such phases through two-photon, two-color photoionization. We found that the harmonics are locked in phase and form a train of 250-attosecond pulses in the time domain. Harmonic generation may be a promising source for attosecond time-resolved measurements.     

The future of attosecond spectroscopy

Attoscience is the study of physical processes that occur in less than a fraction of a cycle of visible light, in times less than a quadrillionth of a second. The motion of electrons inside atoms and molecules that are undergoing photoionization or chemical change falls within this time scale, as does the plasma motion that causes the reflectivity of metals. The techniques to study motion on this scale are based on careful control of strong-field laser-atom interactions. These techniques and new research opportunities in attosecond spectroscopy are reviewed.     

Ultrafast lasers. Strobe light breaks the attosecond barrier

On page 1689 of this issue, physicists report creating the fastest strobe light ever made, with individual pulses lasting just 220 attoseconds, or 220 billionths of a billionth of a second. These unimaginably short pulses are the first to be confirmed as breaking the attosecond barrier, a goal of high-speed-laser researchers for nearly a decade. Such pulses may one day serve as an ultrafast camera, allowing researchers to freeze action and perhaps to spot the gyrations of individual electrons whirling around an atomic nucleus.     

Harnessing attosecond science in the quest for coherent X-rays

Modern laser technology has revolutionized the sensitivity and precision of spectroscopy by providing coherent light in a spectrum spanning the infrared, visible, and ultraviolet wavelength regimes. However, the generation of shorter-wavelength coherent pulses in the x-ray region has proven much more challenging. The recent emergence of high harmonic generation techniques opens the door to this possibility. Here we review the new science that is enabled by an ability to manipulate and control electrons on attosecond time scales, ranging from new tabletop sources of coherent x-rays to an ability to follow complex electron dynamics in molecules and materials. We also explore the implications of these advances for the future of molecular structural characterization schemes that currently rely so heavily on scattering from incoherent x-ray sources.     

Information: the ultimate frontier

Although long-term forecasting is best left to science fiction writers, scientists can illumine basic technological trends, as in the 100-year scenario presented here. Computers will continue the "small is beautiful" trend, but they are not likely to follow the semilog trail because extrapolation from the current base would lead to absurdities such as a computer cost of 3/100 of a cent. To achieve inexpensive high speed and Lilliputian size, new techniques are likely to replace silicon technology. The ultimate computer might be biological and patterned on DNA. Future computers will reacquire information when needed rather than store it, and we will see personalized products at mass production prices. Light wave communication will broaden communications exchange, but software that is more friendly to human users will be needed. By taking over knowledge distribution, electronic information systems will let universities concentrate on new knowledge. More importantly, they will expand everyone's right to information and free expression through the existing media system and to protection from misuse of information by others.     

The approaching era of the tumor suppressor genes

Genes that can inhibit the expression of the tumorigenic phenotype have been detected by the fusion of normal and malignant cells, the phenotypic reversion of in vitro transformants, the induction of terminal differentiation of malignant cell lineages, the loss of "recessive cancer genes," the discovery of regulatory sequences in the immediate vicinity of certain oncogenes, and the inhibition of tumor growth by normal cell products. Such tumor suppressor genes will probably turn out to be as, if not more, diversified as the oncogenes. Consideration of both kinds of genes may reveal common or interrelated functional properties.     

Steering attosecond electron wave packets with light

Photoelectrons excited by extreme ultraviolet or x-ray photons in the presence of a strong laser field generally suffer a spread of their energies due to the absorption and emission of laser photons. We demonstrate that if the emitted electron wave packet is temporally confined to a small fraction of the oscillation period of the interacting light wave, its energy spectrum can be up- or downshifted by many times the laser photon energy without substantial broadening. The light wave can accelerate or decelerate the electron's drift velocity, i.e., steer the electron wave packet like a classical particle. This capability strictly relies on a sub-femtosecond duration of the ionizing x-ray pulse and on its timing to the phase of the light wave with a similar accuracy, offering a simple and potentially single-shot diagnostic tool for attosecond pump-probe spectroscopy.     

The next frontier

High-intensity lasers are opening up a new realm of light-matter interactions. In his Perspective, Yamanouchi reviews recent progress in this field, focusing on two intensity regimes: the Coulombic regime, which mostly deforms molecular structures and causes tunneling ionization, and the relativistic regime, where high-intensity lasers produce x-rays and high-energy particles and may cause nuclear fusion reactions. Efforts are under way to increase laser intensity further for accessing the next frontier.     

The multielectron ionization dynamics underlying attosecond strong-field spectroscopies

Subcycle strong-field ionization (SFI) underlies many emerging spectroscopic probes of atomic or molecular attosecond electronic dynamics. Extending methods such as attosecond high harmonic generation spectroscopy to complex polyatomic molecules requires an understanding of multielectronic excitations, already hinted at by theoretical modeling of experiments on atoms, diatomics, and triatomics. Here, we present a direct method which, independent of theory, experimentally probes the participation of multiple electronic continua in the SFI dynamics of polyatomic molecules. We use saturated (n-butane) and unsaturated (1,3-butadiene) linear hydrocarbons to show how subcycle SFI of polyatomics can be directly resolved into its distinct electronic-continuum channels by above-threshold ionization photoelectron spectroscopy. Our approach makes use of photoelectron-photofragment coincidences, suiting broad classes of polyatomic molecules.