Controlling attosecond electron dynamics by phase-stabilized polarization gating

被引:385
作者
Sola, I. J.
Mevel, E.
Elouga, L.
Constant, E.
Strelkov, V.
Poletto, L.
Villoresi, P.
Benedetti, E.
Caumes, J. -P.
Stagira, S.
Vozzi, C.
Sansone, G.
Nisoli, M.
机构
[1] Univ Bordeaux 1, Ctr Lasers Intenses & Applicat, CEA, CNRS,UMR 5107, F-33405 Talence, France
[2] Russian Acad Sci, Inst Gen Phys, Moscow 119991, Russia
[3] Univ Padua, Dept Informat Engn, Lab Ultraviolet & Xray Opt Res, CNR,INFM, I-35131 Padua, Italy
[4] Politecn Milan, Dept Phys, Natl Lab Ultrafast & Ultraintense Opt Sci, CNR,INFM, I-20133 Milan, Italy
关键词
D O I
10.1038/nphys281
中图分类号
O4 [物理学];
学科分类号
0702 ;
摘要
Attosecond electron wavepackets are produced when an intense laser field ionizes an atom or a molecule(1). 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 possible(2,3), an isolated attosecond pulse is generated. Here we demonstrate that by modulating the polarization of a carrier-envelope phase-stabilized short laser pulse(4), 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 wavefunctions(5,6) and ultrafast dynamics.
引用
收藏
页码:319 / 322
页数:4
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