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  • 1
    Publication Date: 2014-08-29
    Description: Author(s): E. Balogh, B. Bódi, V. Tosa, E. Goulielmakis, K. Varjú, and P. Dombi Optimization of attosecond pulse generation and pulse shaping can result in the generation of ultrashort single and double attosecond pulses with controllable delay which is extremely useful for pump-probe spectroscopy. [Phys. Rev. A 90, 023855] Published Thu Aug 28, 2014
    Keywords: Quantum optics, physics of lasers, nonlinear optics, classical optics
    Print ISSN: 1050-2947
    Electronic ISSN: 1094-1622
    Topics: Physics
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  • 2
    Publication Date: 2015-05-29
    Description: Extreme ultraviolet (EUV) high-harmonic radiation emerging from laser-driven atoms, molecules or plasmas underlies powerful attosecond spectroscopy techniques and provides insight into fundamental structural and dynamic properties of matter. The advancement of these spectroscopy techniques to study strong-field electron dynamics in condensed matter calls for the generation and manipulation of EUV radiation in bulk solids, but this capability has remained beyond the reach of optical sciences. Recent experiments and theoretical predictions paved the way to strong-field physics in solids by demonstrating the generation and optical control of deep ultraviolet radiation in bulk semiconductors, driven by femtosecond mid-infrared fields or the coherent up-conversion of terahertz fields to multi-octave spectra in the mid-infrared and optical frequencies. Here we demonstrate that thin films of SiO2 exposed to intense, few-cycle to sub-cycle pulses give rise to wideband coherent EUV radiation extending in energy to about 40 electronvolts. Our study indicates the association of the emitted EUV radiation with intraband currents of multi-petahertz frequency, induced in the lowest conduction band of SiO2. To demonstrate the applicability of high-harmonic spectroscopy to solids, we exploit the EUV spectra to gain access to fine details of the energy dispersion profile of the conduction band that are as yet inaccessible by photoemission spectroscopy in wide-bandgap dielectrics. In addition, we use the EUV spectra to trace the attosecond control of the intraband electron motion induced by synthesized optical transients. Our work advances lightwave electronics in condensed matter into the realm of multi-petahertz frequencies and their attosecond control, and marks the advent of solid-state EUV photonics.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Luu, T T -- Garg, M -- Kruchinin, S Yu -- Moulet, A -- Hassan, M Th -- Goulielmakis, E -- England -- Nature. 2015 May 28;521(7553):498-502. doi: 10.1038/nature14456.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Max-Planck-Institut fur Quantenoptik, Hans-Kopfermann-Strasse 1, D-85748 Garching, Germany.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/26017451" target="_blank"〉PubMed〈/a〉
    Print ISSN: 0028-0836
    Electronic ISSN: 1476-4687
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
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  • 3
    Publication Date: 2011-09-10
    Description: Manipulation of electron dynamics calls for electromagnetic forces that can be confined to and controlled over sub-femtosecond time intervals. Tailored transients of light fields can provide these forces. We report on the generation of subcycle field transients spanning the infrared, visible, and ultraviolet frequency regimes with a 1.5-octave three-channel optical field synthesizer and their attosecond sampling. To demonstrate applicability, we field-ionized krypton atoms within a single wave crest and launched a valence-shell electron wavepacket with a well-defined initial phase. Half-cycle field excitation and attosecond probing revealed fine details of atomic-scale electron motion, such as the instantaneous rate of tunneling, the initial charge distribution of a valence-shell wavepacket, the attosecond dynamic shift (instantaneous ac Stark shift) of its energy levels, and its few-femtosecond coherent oscillations.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Wirth, A -- Hassan, M Th -- Grguras, I -- Gagnon, J -- Moulet, A -- Luu, T T -- Pabst, S -- Santra, R -- Alahmed, Z A -- Azzeer, A M -- Yakovlev, V S -- Pervak, V -- Krausz, F -- Goulielmakis, E -- New York, N.Y. -- Science. 2011 Oct 14;334(6053):195-200. doi: 10.1126/science.1210268. Epub 2011 Sep 8.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Max-Planck-Institut fur Quantenoptik (MPQ), Garching, Germany.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/21903778" target="_blank"〉PubMed〈/a〉
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 4
    Publication Date: 2004-08-31
    Description: The electromagnetic field of visible light performs approximately 10(15) oscillations per second. Although many instruments are sensitive to the amplitude and frequency (or wavelength) of these oscillations, they cannot access the light field itself. We directly observed how the field built up and disappeared in a short, few-cycle pulse of visible laser light by probing the variation of the field strength with a 250-attosecond electron burst. Our apparatus allows complete characterization of few-cycle waves of visible, ultraviolet, and/or infrared light, thereby providing the possibility for controlled and reproducible synthesis of ultrabroadband light waveforms.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Goulielmakis, E -- Uiberacker, M -- Kienberger, R -- Baltuska, A -- Yakovlev, V -- Scrinzi, A -- Westerwalbesloh, Th -- Kleineberg, U -- Heinzmann, U -- Drescher, M -- Krausz, F -- New York, N.Y. -- Science. 2004 Aug 27;305(5688):1267-9.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Institut fur Photonik, Technische Universitat Wien, Gusshausstrasse 27, A-1040 Wien, Austria.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15333834" target="_blank"〉PubMed〈/a〉
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 5
    Publication Date: 2010-08-06
    Description: The superposition of quantum states drives motion on the atomic and subatomic scales, with the energy spacing of the states dictating the speed of the motion. In the case of electrons residing in the outer (valence) shells of atoms and molecules which are separated by electronvolt energies, this means that valence electron motion occurs on a subfemtosecond to few-femtosecond timescale (1 fs = 10(-15) s). In the absence of complete measurements, the motion can be characterized in terms of a complex quantity, the density matrix. Here we report an attosecond pump-probe measurement of the density matrix of valence electrons in atomic krypton ions. We generate the ions with a controlled few-cycle laser field and then probe them through the spectrally resolved absorption of an attosecond extreme-ultraviolet pulse, which allows us to observe in real time the subfemtosecond motion of valence electrons over a multifemtosecond time span. We are able to completely characterize the quantum mechanical electron motion and determine its degree of coherence in the specimen of the ensemble. Although the present study uses a simple, prototypical open system, attosecond transient absorption spectroscopy should be applicable to molecules and solid-state materials to reveal the elementary electron motions that control physical, chemical and biological properties and processes.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Goulielmakis, Eleftherios -- Loh, Zhi-Heng -- Wirth, Adrian -- Santra, Robin -- Rohringer, Nina -- Yakovlev, Vladislav S -- Zherebtsov, Sergey -- Pfeifer, Thomas -- Azzeer, Abdallah M -- Kling, Matthias F -- Leone, Stephen R -- Krausz, Ferenc -- England -- Nature. 2010 Aug 5;466(7307):739-43. doi: 10.1038/nature09212.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Max-Planck-Institut fur Quantenoptik, Hans-Kopfermann-Strasse 1, D-85748 Garching, Germany. elgo@mpq.mpg.de〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/20686571" target="_blank"〉PubMed〈/a〉
    Print ISSN: 0028-0836
    Electronic ISSN: 1476-4687
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
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  • 6
    Publication Date: 2007-08-11
    Description: Electrons emit light, carry electric current, and bind atoms together to form molecules. Insight into and control of their atomic-scale motion are the key to understanding the functioning of biological systems, developing efficient sources of x-ray light, and speeding up electronics. Capturing and steering this electron motion require attosecond resolution and control, respectively (1 attosecond = 10(-18) seconds). A recent revolution in technology has afforded these capabilities: Controlled light waves can steer electrons inside and around atoms, marking the birth of lightwave electronics. Isolated attosecond pulses, well reproduced and fully characterized, demonstrate the power of the new technology. Controlled few-cycle light waves and synchronized attosecond pulses constitute its key tools. We review the current state of lightwave electronics and highlight some future directions.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Goulielmakis, E -- Yakovlev, V S -- Cavalieri, A L -- Uiberacker, M -- Pervak, V -- Apolonski, A -- Kienberger, R -- Kleineberg, U -- Krausz, F -- New York, N.Y. -- Science. 2007 Aug 10;317(5839):769-75.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Max-Planck-Institut fur Quantenoptik, Hans-Kopfermann-Strasse 1, D-85748 Garching, Germany.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17690286" target="_blank"〉PubMed〈/a〉
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 7
    Publication Date: 2008-06-21
    Description: Nonlinear optics plays a central role in the advancement of optical science and laser-based technologies. We report on the confinement of the nonlinear interaction of light with matter to a single wave cycle and demonstrate its utility for time-resolved and strong-field science. The electric field of 3.3-femtosecond, 0.72-micron laser pulses with a controlled and measured waveform ionizes atoms near the crests of the central wave cycle, with ionization being virtually switched off outside this interval. Isolated sub-100-attosecond pulses of extreme ultraviolet light (photon energy approximately 80 electron volts), containing approximately 0.5 nanojoule of energy, emerge from the interaction with a conversion efficiency of approximately 10(-6). These tools enable the study of the precision control of electron motion with light fields and electron-electron interactions with a resolution approaching the atomic unit of time ( approximately 24 attoseconds).〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Goulielmakis, E -- Schultze, M -- Hofstetter, M -- Yakovlev, V S -- Gagnon, J -- Uiberacker, M -- Aquila, A L -- Gullikson, E M -- Attwood, D T -- Kienberger, R -- Krausz, F -- Kleineberg, U -- New York, N.Y. -- Science. 2008 Jun 20;320(5883):1614-7. doi: 10.1126/science.1157846.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Max-Planck-Institut fur Quantenoptik, Hans-Kopfermann-Strasse 1, D-85748 Garching, Germany. elgo@mpq.mpg.de〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/18566281" target="_blank"〉PubMed〈/a〉
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 8
    Publication Date: 2010-06-26
    Description: Photoemission from atoms is assumed to occur instantly in response to incident radiation and provides the basis for setting the zero of time in clocking atomic-scale electron motion. We used attosecond metrology to reveal a delay of 21 +/- 5 attoseconds in the emission of electrons liberated from the 2p orbitals of neon atoms with respect to those released from the 2s orbital by the same 100-electron volt light pulse. Small differences in the timing of photoemission from different quantum states provide a probe for modeling many-electron dynamics. Theoretical models refined with the help of attosecond timing metrology may provide insight into electron correlations and allow the setting of the zero of time in atomic-scale chronoscopy with a precision of a few attoseconds.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Schultze, M -- Fiess, M -- Karpowicz, N -- Gagnon, J -- Korbman, M -- Hofstetter, M -- Neppl, S -- Cavalieri, A L -- Komninos, Y -- Mercouris, Th -- Nicolaides, C A -- Pazourek, R -- Nagele, S -- Feist, J -- Burgdorfer, J -- Azzeer, A M -- Ernstorfer, R -- Kienberger, R -- Kleineberg, U -- Goulielmakis, E -- Krausz, F -- Yakovlev, V S -- New York, N.Y. -- Science. 2010 Jun 25;328(5986):1658-62. doi: 10.1126/science.1189401.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department fur Physik, Ludwig-Maximilians-Universitat, Am Coulombwall 1, D-85748 Garching, Germany. Martin.Schultze@mpq.mpg.de〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/20576884" target="_blank"〉PubMed〈/a〉
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 9
    Publication Date: 2016-02-06
    Description: The time it takes a bound electron to respond to the electromagnetic force of light sets a fundamental speed limit on the dynamic control of matter and electromagnetic signal processing. Time-integrated measurements of the nonlinear refractive index of matter indicate that the nonlinear response of bound electrons to optical fields is not instantaneous; however, a complete spectral characterization of the nonlinear susceptibility tensors--which is essential to deduce the temporal response of a medium to arbitrary driving forces using spectral measurements--has not yet been achieved. With the establishment of attosecond chronoscopy, the impulsive response of positive-energy electrons to electromagnetic fields has been explored through ionization of atoms and solids by an extreme-ultraviolet attosecond pulse or by strong near-infrared fields. However, none of the attosecond studies carried out so far have provided direct access to the nonlinear response of bound electrons. Here we demonstrate that intense optical attosecond pulses synthesized in the visible and nearby spectral ranges allow sub-femtosecond control and metrology of bound-electron dynamics. Vacuum ultraviolet spectra emanating from krypton atoms, exposed to intense waveform-controlled optical attosecond pulses, reveal a finite nonlinear response time of bound electrons of up to 115 attoseconds, which is sensitive to and controllable by the super-octave optical field. Our study could enable new spectroscopies of bound electrons in atomic, molecular or lattice potentials of solids, as well as light-based electronics operating on sub-femtosecond timescales and at petahertz rates.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Hassan, M Th -- Luu, T T -- Moulet, A -- Raskazovskaya, O -- Zhokhov, P -- Garg, M -- Karpowicz, N -- Zheltikov, A M -- Pervak, V -- Krausz, F -- Goulielmakis, E -- England -- Nature. 2016 Feb 4;530(7588):66-70. doi: 10.1038/nature16528.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Max-Planck-Institut fur Quantenoptik, Hans-Kopfermann-Strasse 1, D-85748 Garching, Germany. ; Department fur Physik, Ludwig-Maximilians-Universitat, Am Coulombwall 1, D-85748 Garching, Germany. ; Department of Physics and Astronomy, Texas A&M University, College Station, Texas 77843, USA. ; Physics Department, International Laser Center, M.V. Lomonosov Moscow State University, 119992 Moscow, Russia.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/26842055" target="_blank"〉PubMed〈/a〉
    Print ISSN: 0028-0836
    Electronic ISSN: 1476-4687
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
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  • 10
    Publication Date: 2016-10-20
    Description: Multi-petahertz electronic metrology Nature 538, 7625 (2016). doi:10.1038/nature19821 Authors: M. Garg, M. Zhan, T. T. Luu, H. Lakhotia, T. Klostermann, A. Guggenmos & E. Goulielmakis The frequency of electric currents associated with charge carriers moving in the electronic bands of solids determines the speed limit of electronics and thereby that of information and signal processing. The use of light fields to drive electrons promises access to vastly higher frequencies than conventionally used, as electric currents can be induced and manipulated on timescales faster than that of the quantum dephasing of charge carriers in solids. This forms the basis of terahertz (1012 hertz) electronics in artificial superlattices, and has enabled light-based switches and sampling of currents extending in frequency up to a few hundred terahertz. Here we demonstrate the extension of electronic metrology to the multi-petahertz (1015 hertz) frequency range. We use single-cycle intense optical fields (about one volt per ångström) to drive electron motion in the bulk of silicon dioxide, and then probe its dynamics by using attosecond (10−18 seconds) streaking to map the time structure of emerging isolated attosecond extreme ultraviolet transients and their optical driver. The data establish a firm link between the emission of the extreme ultraviolet radiation and the light-induced intraband, phase-coherent electric currents that extend in frequency up to about eight petahertz, and enable access to the dynamic nonlinear conductivity of silicon dioxide. Direct probing, confinement and control of the waveform of intraband currents inside solids on attosecond timescales establish a method of realizing multi-petahertz coherent electronics. We expect this technique to enable new ways of exploring the interplay between electron dynamics and the structure of condensed matter on the atomic scale.
    Print ISSN: 0028-0836
    Electronic ISSN: 1476-4687
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Published by Springer Nature
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