...
首页> 外文期刊>The Journal of Chemical Physics >Two-dimensional Fourier transform electronic spectroscopy at a conical intersection
【24h】

Two-dimensional Fourier transform electronic spectroscopy at a conical intersection

机译:圆锥形相交处的二维傅立叶变换电子光谱

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

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 twodimensional 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. ? 2014 Author(s). All article content, except where otherwise noted, is licensed under a Creative Commons Attribution 3.0 Unported License.
机译:我们报告了对苯甲腈中的硅萘酞菁(SiNc)的二维(2D)电子光谱的测量和建模,该系统的极化各向异性揭示了在约100 fs内通过正方形对称的Jahn-Teller圆锥形交叉点[D. A. Farrow,W。Qian,E。R. Smith,A。A. Ferro和D. M. Jonas,J。Chem。物理128,144510(2008)]。测得的2D傅里叶变换(FT)光谱表明在类似的时间尺度上电子相干性的损失。飞秒振动通过圆锥形漏斗产生的2D光谱是通过对耦合的电子和振动动力学进行完全非绝热处理来建模的,这两个对振子既引起电子退相干又发生了人口迁移,但未衰减。通过仅将简并的振动本征态分配给两个电子态之一的对称响应函数,就可以将分析阻尼函数纳入其他仅能引起退相干或种群转移的阻尼Jahn-Teller主动模式。弗兰克-康登主动完全对称模式被纳入分析。计算结果表明,仅这些圆锥形相交动力学就无法破坏在实验观察到的时标上最初准备的波包的相干性,并且无法预测到约200 fs的光子回波切片会出现未观测到的复发。与实验二维电子光谱的一致性要求完全对称的振动动力学在使回波切片在约100 fs的时标上衰减方面发挥作用。当包含一个稳定能量为〜2 cm〜(?1)的“不对称溶剂化模式”时,该扩展模型还重现了SiNc中约100 fs的超快电子各向异性衰减。尽管计算表明激发态之间的能隙不均匀可以加宽对角线2D线形,但对角线宽度由SiNc中完全对称的振动运动控制。对于此浅圆锥形相交点,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。 ? 2014年作者。除另有说明外,所有文章内容均根据知识共享署名3.0未移植许可证进行许可。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号