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在圆锥交叉点处的二维傅里叶变换电子光谱学。

Two-dimensional Fourier transform electronic spectroscopy at a conical intersection.

机构信息

Department of Chemistry and Biochemistry, University of Colorado, 215 UCB, Boulder, Colorado 80309, USA.

出版信息

J Chem Phys. 2014 Mar 28;140(12):124312. doi: 10.1063/1.4867996.

Abstract

We report measurement and modeling of two-dimensional (2D) electronic spectra of a silicon naphthalocyanine (SiNc) in benzonitrile, a system for which the polarization anisotropy reveals passage through a square-symmetric Jahn-Teller conical intersection in ∼100 fs [D. A. Farrow, W. Qian, E. R. Smith, A. A. Ferro, and D. M. Jonas, J. Chem. Phys. 128, 144510 (2008)]. The measured 2D Fourier transform (FT) spectra indicate loss of electronic coherence on a similar timescale. The 2D spectra arising from femtosecond vibronic dynamics through the conical funnel are modeled by full non-adiabatic treatment of the coupled electronic and vibrational dynamics for a pair of un-damped Jahn-Teller active vibrations responsible for both electronic decoherence and population transfer. Additional damped Jahn-Teller active modes that can cause only decoherence or population transfer are treated with analytical response functions that can be incorporated into the numerical non-adiabatic calculation by exploiting symmetry assignment of degenerate vibronic eigenstates to one of two electronic states. Franck-Condon active totally symmetric modes are incorporated analytically. The calculations reveal that these conical intersection dynamics alone are incapable of destroying the coherence of the initially prepared wavepacket on the experimentally observed timescale and predict an unobserved recurrence in the photon echo slice at ∼200 fs. Agreement with the experimental two-dimensional electronic spectra necessitates a role for totally symmetric vibrational dynamics in causing the echo slice to decay on a ∼100 fs timescale. This extended model also reproduces the ∼100 fs ultrafast electronic anisotropy decay in SiNc when an "asymmetric solvation mode" with a small stabilization energy of ∼2 cm(-1) is included. Although calculations show that inhomogeneities in the energy gap between excited states can broaden the anti-diagonal 2D lineshape, the anti-diagonal width is dominated by totally symmetric vibrational motions in SiNc. For this shallow conical intersection, the non-adiabatic dynamics destroy electronic coherence more slowly than they destroy electronic alignment.

摘要

我们报告了硅萘酞菁(SiNc)在苯腈中的二维(2D)电子光谱的测量和建模,该系统的极化各向异性表明在大约 100fs 内通过了一个正方形对称的 Jahn-Teller 锥形交叉[D. A. Farrow、W. Qian、E. R. Smith、A. A. Ferro 和 D. M. Jonas,J. Chem. Phys. 128,144510(2008)]。测量的 2D 傅里叶变换(FT)光谱表明电子相干性在类似的时间尺度上丧失。通过锥形漏斗的飞秒振动态动力学产生的 2D 光谱通过对一对非阻尼 Jahn-Teller 活性振动的电子和振动动力学进行全非绝热处理来建模,这对振动负责电子去相干和种群转移。通过利用简并振动态的对称分配将额外的阻尼 Jahn-Teller 活性模式(只能导致去相干或种群转移)处理为解析响应函数,可以将其合并到数值非绝热计算中两个电子态之一的简并振动态。Franck-Condon 活性全对称模式通过解析方法进行合并。该计算表明,这些锥形交叉动力学本身无法在实验观察到的时间尺度上破坏初始制备的波包的相干性,并预测在大约 200fs 处未观察到光子回波切片的重现。与实验二维电子光谱的一致性要求全对称振动动力学在大约 100fs 的时间尺度上使回波切片衰减。当包含具有约 2cm(-1)的小稳定能的“不对称溶剂化模式”时,这种扩展模型还可以再现 SiNc 中约 100fs 的超快电子各向异性衰减。尽管计算表明,在激发态之间的能量间隙中的不均匀性可以加宽反对角线 2D 线宽,但 SiNc 中的反对角线宽度主要由全对称振动运动决定。对于这种浅锥形交叉,非绝热动力学破坏电子相干性的速度比破坏电子对准的速度慢。

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