期刊文献+

Use of photoelectron energy spectrum transfer equation for the measurement of a narrowband XUV pulse

Use of photoelectron energy spectrum transfer equation for the measurement of a narrowband XUV pulse
原文传递
导出
摘要 To study the time evolution of a molecular state in an ultra-fast chemical reaction,the use of shorter pulses with higher photon energy and narrower bandwidth for both pump and probe is necessary.However,quick and precise measurement of their detailed time structures is a challenge.Over the last decade,great efforts have been made to measure an attosecond extreme ultraviolet (XUV) pulse.To date,several methods have been developed to measure the pulse duration and completely reconstruct it.The attosecond spectral phase interferometry for direct electric field reconstruction (SPIDER) and attosecond frequency-resolved optical gating (FROG) techniques are often used.However,these methods use state-of-the-art experimental set-ups and complicated data analysis procedures.To develop attosecond metrology for practical use (e.g.timing,measurement,evaluation,calibration,optimization,pumping,probing),we propose a quick and analytical method to precisely observe an attosecond XUV pulse with laser-assisted photo-ionization.The method is based on determining the laser-related phase of each streaked electron and using a transfer equation for one-step pulse reconstruction without any time-resolved measurements,iterative calculations,or data fitting procedures.Temporal errors of the pulse reconstruction are calculated from the XUV bandwidth.Because the transfer equation establishes a direct connection between the XUV pulse properties,the crucial laser parameters (peak intensity,phase,carrier envelope phase),the atomic ionization potential,and the measured photoelectron energy spectrum,we can use it to study any one of these properties from other known information and probe the dynamic processes of an ultra-fast reaction. To study the time evolution of a molecular state in an ultrafast chemical reaction, the use of shorter pulses with higher photon energy and narrower bandwidth for both pump and probe is necessary. However, quick and precise measurement of their detailed time struc tures is a challenge. Over the last decade, great efforts have been made to measure an attosecond extreme ultraviolet (XUV) pulse. To date, several methods have been developed to measure the pulse duration and completely reconstruct it. The attosecond spectral phase interferometry for direct electric field reconstruction (SPIDER) and attosecond frequencyresolved optical gating (FROG) tech niques are often used. However, these methods use stateoftheart experimental setups and complicated data analysis procedures. To develop attosecond metrology for practical use (e.g. timing, measurement, evaluation, calibration, optimization, pumping, probing), we propose a quick and analytical method to precisely observe an attosecond XUV pulse with laserassisted photoionization. The method is based on determining the laserrelated phase of each streaked electron and using a transfer equation for onestep pulse re construction without any timeresolved measurements, iterative calculations, or data fitting procedures. Temporal errors of the pulse reconstruction are calculated from the XUV bandwidth. Because the transfer equation establishes a direct connection between the XUV pulse properties, the crucial laser parameters (peak intensity, phase, carrier envelope phase), the atomic ionization potential, and the measured photoelectron energy spectrum, we can use it to study any one of these properties from other known information and probe the dynamic processes of an ultrafast reaction.
出处 《Chinese Science Bulletin》 SCIE CAS 2012年第8期843-848,共6页
基金 supported by the National Natural Science Foundation of China (10827505 and 10675014)
关键词 时间分辨测量 光电子能谱 远紫外线 传输方程 短脉冲 窄带 超快化学反应 脉冲持续时间 attosecond measurement photoelectron energy spectrum laser phase determination method transfer equation
  • 相关文献

参考文献35

  • 1Drescher M, Hentschel M, Kienberger R, et al. X-ray pulses approaching the attosecond frontier. Science, 2001, 291:1923-1927.
  • 2Hentschel M, Kienberger R, Spielmann Ch, et al. Attosecond metrology. Nature, 2001, 414:509-513.
  • 3Drescher M, Hentschel M, Kienberger R, et al. Time-resolved atomic inner-shell spectroscopy. Nature, 2002, 419:803-807.
  • 4Kienberger R, Goulielmakies E, Uiberacker M, et al. Atomic transient recorder. Nature, 2004, 427:817-821.
  • 5Goulielmakis E, Uiberacker M, Kienberger R, et al. Direct measurement of light waves. Science, 2004, 305:1267-1269.
  • 6Sansone G, Benedetti E, Calegari F, et al. Isolated single-cycle attosecond pulses. Science, 2006, 314:443-446.
  • 7Spielmann Ch, Burnett N H. Generation of coherent X-rays in the water window using 5-femtosecond laser pulses. Science, 1997, 278: 661- 664.
  • 8Schnurer M, Spielmann Ch, Wobrauschek P, et al. Coherent 0.5-keV X-ray emission from helium driven by a sub-10-fs laser. Phys Rev Lett, 1998, 80:3236-3239.
  • 9Kienberger R, Goulielmakis E, Uiberacker M, et al. Single sub-fs soft- X-ray pulses: Generation and measurement with the atomic transient recorder. J Mod Opt, 2005, 52:261-275.
  • 10Mairesse Y, Bohan A D, Frasinski L J, et al. Optimization ofattosecond pulse generation. Phys Rev Lett, 2004, 93:163901-163904.

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部