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Salvatore Stagira

Other affiliations: University of Padua, National Research Council, Leonardo  ...read more
Bio: Salvatore Stagira is an academic researcher from Polytechnic University of Milan. The author has contributed to research in topics: High harmonic generation & Laser. The author has an hindex of 39, co-authored 308 publications receiving 7801 citations. Previous affiliations of Salvatore Stagira include University of Padua & National Research Council.


Papers
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Journal ArticleDOI
20 Oct 2006-Science
TL;DR: 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 attose Cond pulses rather than by their intensity profile.
Abstract: We generated single-cycle isolated attosecond pulses around ∼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.

1,386 citations

Journal ArticleDOI
08 Nov 2001-Nature
TL;DR: Here, a technique that does not require phase stabilization is used to demonstrate experimentally the influence of the absolute phase of a short laser pulse on the emission of photoelectrons.
Abstract: Currently, the shortest laser pulses1 that can be generated in the visible spectrum consist of fewer than two optical cycles (measured at the full-width at half-maximum of the pulse's envelope). The time variation of the electric field in such a pulse depends on the phase of the carrier frequency with respect to the envelope—the absolute phase. Because intense laser–matter interactions generally depend on the electric field of the pulse, the absolute phase is important for a number of nonlinear processes2,3,4,5,6,7,8. But clear evidence of absolute-phase effects has yet to be detected experimentally, largely because of the difficulty of stabilizing the absolute phase in powerful laser pulses. Here we use a technique that does not require phase stabilization to demonstrate experimentally the influence of the absolute phase of a short laser pulse on the emission of photoelectrons. Atoms are ionized by a short laser pulse, and the photoelectrons are recorded with two opposing detectors in a plane perpendicular to the laser beam. We detect an anticorrelation in the shot-to-shot analysis of the electron yield.

570 citations

Journal ArticleDOI
TL;DR: In this article, the polarization of a carrier-envelope phase-stabilized short laser pulse is modulated to fine control the electron-wavepacket dynamics, and the signature of a single return of the electron wavepacket over a large range of energies is observed.
Abstract: Attosecond electron wavepackets are produced when an intense laser field ionizes an atom or a molecule1. When the laser field drives the wavepackets back to the parent ion, they interfere with the bound wavefunction, producing coherent subfemtosecond extreme-ultraviolet light bursts. When only a single return is possible2,3, an isolated attosecond pulse is generated. Here we demonstrate that by modulating the polarization of a carrier-envelope phase-stabilized short laser pulse4, we can finely control the electron-wavepacket dynamics. We use high-order harmonic generation to probe these dynamics. Under optimized conditions, we observe the signature of a single return of the electron wavepacket over a large range of energies. This temporally confines the extreme-ultraviolet emission to an isolated attosecond pulse with a broad and tunable bandwidth. Our approach is very general, and extends the bandwidth of attosecond isolated pulses in such a way that pulses of a few attoseconds seem achievable. Similar temporal resolution could also be achieved by directly using the broadband electron wavepacket. This opens up a new regime for time-resolved tomography of atomic or molecular wavefunctions5,6 and ultrafast dynamics.

410 citations

Journal ArticleDOI
TL;DR: In this article, a review of recent advances in attosecond science is reported and important applications are discussed, with a brief presentation of various techniques that can be employed for the generation and diagnosis of sub-femtosecond pulses.
Abstract: Attosecond science offers formidable tools for the investigation of electronic processes at the heart of important physical processes in atomic, molecular and solid-state physics. In the last 15 years impressive advances have been obtained from both the experimental and theoretical points of view. Attosecond pulses, in the form of isolated pulses or of trains of pulses, are now routinely available in various laboratories. In this review recent advances in attosecond science are reported and important applications are discussed. After a brief presentation of various techniques that can be employed for the generation and diagnosis of sub-femtosecond pulses, various applications are reported in atomic, molecular and condensed-matter physics.

351 citations

Journal ArticleDOI
TL;DR: In this article, a technique that can be applied to more complicated molecules is presented, which can be used to map electron orbitals and provide information about the inner workings of the molecules.
Abstract: Atomic and molecular gases generate extreme ultraviolet light when excited by pulses of intense laser light. This emission provides information about the inner workings of the molecules and even enables us to map electron orbitals. However, so far molecular orbital tomography has been restricted to simple molecules. A technique that can be applied to more complicated molecules is now unveiled.

302 citations


Cited by
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Journal ArticleDOI

[...]

08 Dec 2001-BMJ
TL;DR: There is, I think, something ethereal about i —the square root of minus one, which seems an odd beast at that time—an intruder hovering on the edge of reality.
Abstract: There is, I think, something ethereal about i —the square root of minus one. I remember first hearing about it at school. It seemed an odd beast at that time—an intruder hovering on the edge of reality. Usually familiarity dulls this sense of the bizarre, but in the case of i it was the reverse: over the years the sense of its surreal nature intensified. It seemed that it was impossible to write mathematics that described the real world in …

33,785 citations

Journal ArticleDOI
TL;DR: The interest in nanoscale materials stems from the fact that new properties are acquired at this length scale and, equally important, that these properties are equally important.
Abstract: The interest in nanoscale materials stems from the fact that new properties are acquired at this length scale and, equally important, that these properties * To whom correspondence should be addressed. Phone, 404-8940292; fax, 404-894-0294; e-mail, mostafa.el-sayed@ chemistry.gatech.edu. † Case Western Reserve UniversitysMillis 2258. ‡ Phone, 216-368-5918; fax, 216-368-3006; e-mail, burda@case.edu. § Georgia Institute of Technology. 1025 Chem. Rev. 2005, 105, 1025−1102

6,852 citations

Journal Article
TL;DR: In this article, a fast Fourier transform method of topography and interferometry is proposed to discriminate between elevation and depression of the object or wave-front form, which has not been possible by the fringe-contour generation techniques.
Abstract: A fast-Fourier-transform method of topography and interferometry is proposed. By computer processing of a noncontour type of fringe pattern, automatic discrimination is achieved between elevation and depression of the object or wave-front form, which has not been possible by the fringe-contour-generation techniques. The method has advantages over moire topography and conventional fringe-contour interferometry in both accuracy and sensitivity. Unlike fringe-scanning techniques, the method is easy to apply because it uses no moving components.

3,742 citations

Journal ArticleDOI
TL;DR: Some of the observed new chemical, optical, and thermal properties of metallic nanocrystals when their size is confined to the nanometer length scale and their dynamical processes are observed on the femto- to picosecond time scale are described.
Abstract: The properties of a material depend on the type of motion its electrons can execute, which depends on the space available for them (i.e., on the degree of their spatial confinement). Thus, the properties of each material are characterized by a specific length scale, usually on the nanometer dimension. If the physical size of the material is reduced below this length scale, its properties change and become sensitive to its size and shape. In this Account we describe some of the observed new chemical, optical, and thermal properties of metallic nanocrystals when their size is confined to the nanometer length scale and their dynamical processes are observed on the femto- to picosecond time scale.

2,655 citations

Journal ArticleDOI
14 Mar 2002-Nature
TL;DR: The ability to count optical oscillations of more than 1015 cycles per second facilitates high-precision optical spectroscopy, and has led to the construction of an all-optical atomic clock that is expected eventually to outperform today's state-of-the-art caesium clocks.
Abstract: Extremely narrow optical resonances in cold atoms or single trapped ions can be measured with high resolution. A laser locked to such a narrow optical resonance could serve as a highly stable oscillator for an all-optical atomic clock. However, until recently there was no reliable clockwork mechanism that could count optical frequencies of hundreds of terahertz. Techniques using femtosecond-laser frequency combs, developed within the past few years, have solved this problem. The ability to count optical oscillations of more than 1015 cycles per second facilitates high-precision optical spectroscopy, and has led to the construction of an all-optical atomic clock that is expected eventually to outperform today's state-of-the-art caesium clocks.

2,612 citations