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首页> 外文期刊>The Journal of Chemical Physics >Experimental distinction between phase shifts and time delays: Implications for femtosecond spectroscopy and coherent control of chemical reactions
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Experimental distinction between phase shifts and time delays: Implications for femtosecond spectroscopy and coherent control of chemical reactions

机译:相移和时延之间的实验区别:飞秒光谱学和化学反应的相干控制的意义

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Two different definitions of phase shifts and time delays are contrasted and shown to match different experimental methods of generating delayed pulses. Phase shifts and time delays are usually defined in terms of a carrier wave in magnetic resonance, but definitions based on the envelope of a single pulse are useful in optics. It is demonstrated experimentally that a frequency domain measurement using spectral interferometry can simultaneously measure phase shifts with an accuracy of 0.1 rad (2#sigma#) and time delays with a precision of 40 attoseconds (2#sigma#) for 25 femtosecond optical pulses. Envelope time delays are generated by pathlength differences in an interferometer. Constant spectral phase shifts are demonstrated by diffracting pulses from a variable phase volume diffraction grating. Experimental requirements for phase-resolved spectroscopy are outlined. The theory of phase-locked pulse pair techniques is reexamined, and it is concluded that linear experiments with phase-locked pulse pairs are completely equivalent to Fourier transform absorption spectroscopy and do not measure the refractive index or real part of the susceptibility. It is shown that Fourier sine and cosine transformations of truncated time domain signals which do not match the symmetry of the complete signal can produce a false dispersive susceptibility because they are equivalent to Kramers-Kronig inversion of finite bandwidth absorption data. A procedure for shifting #pi#/2 phase-locked transients by a quarter cycle of delay to generate a transient with a #pi#/2 spectral phase shift is given. Equations used to calculate femtosecond nonlinear optical signals have assumed carrier wave delays. Modifications to these equations are required when envelope delays are generated by interferometer pathlength differences and modified equations are given. The modified equations yield significantly different results for phase-resolved or interferometric experiments. In particular, the modified equations are needed to calculate indirectly (interferometrically) detected frequencies and the real and imaginary parts of two-dimensional Fourier transform spectra. The role of the refractive index and real part of the frequency domain susceptibility in nonlinear experiments with phase-locked pulse pairs is explored. It is concluded that experiments such as the heterodyne detected stimulated photon echo are insensitive to nonlinear refractive index changes under some circumstances. Finally, modifications of some equations used in the theory of coherent control are needed to match theory with experimental practice.
机译:对相移和时间延迟的两种不同定义进行了对比,并显示为与生成延迟脉冲的不同实验方法相匹配。通常根据磁共振中的载波来定义相移和时间延迟,但是基于单个脉冲的包络的定义在光学中很有用。实验证明,使用频谱干涉术的频域测量可以同时测量25飞秒光脉冲的相移,精度为0.1 rad(2#sigma#),时延的精度为40阿秒(2#sigma#)。包络时间延迟是由干涉仪中的光程差产生的。恒定的光谱相移由来自可变相体积衍射光栅的脉冲衍射证明。概述了相分辨光谱的实验要求。重新研究了锁相脉冲对技术的理论,得出的结论是,使用锁相脉冲对的线性实验完全等同于傅立叶变换吸收光谱,并且不测量折射率或磁化率的实部。结果表明,与完整信号的对称性不匹配的截断时域信号的傅立叶正弦和余弦变换会产生错误的色散敏感性,因为它们等效于有限带宽吸收数据的Kramers-Kronig反演。给出了将#pi#/ 2锁相瞬变移位四分之一延迟周期以生成具有#pi#/ 2频谱相移的瞬变的过程。用于计算飞秒非线性光信号的方程式假定了载波延迟。当通过干涉仪光程差产生包络延迟并给出修改后的方程时,需要对这些方程进行修改。对于相位分辨实验或干涉测量实验,修改后的方程会产生明显不同的结果。特别地,需要修改后的方程式来间接地(干涉地)计算检测到的频率以及二维傅立叶变换谱的实部和虚部。探索了在具有锁相脉冲对的非线性实验中折射率和频域磁化率实部的作用。结论是,在某些情况下,诸如外差检测到的受激光子回波之类的实验对非线性折射率变化不敏感。最后,需要对相干控制理论中使用的一些方程进行修改,以使理论与实验实践相匹配。

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