首页> 外文学位 >Femtosecond Multidimensional Electronic and Raman Spectroscopy towards the Study of Mn Complexes and the Oxygen Evolving Complex: Developing Understanding of Femtosecond Light Generation and Applying Femtosecond Multidimensional Electronic and Raman Spectroscopies to Model Systems.
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Femtosecond Multidimensional Electronic and Raman Spectroscopy towards the Study of Mn Complexes and the Oxygen Evolving Complex: Developing Understanding of Femtosecond Light Generation and Applying Femtosecond Multidimensional Electronic and Raman Spectroscopies to Model Systems.

机译:飞秒多维电子和拉曼光谱研究锰配合物和析氧复合物:发展对飞秒光产生的理解,并将飞秒多维电子和拉曼光谱学应用于模型系统。

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摘要

The oxygen evolving complex of photosystem II is a tetramanganese complex that catalyzes the oxidation of water to dioxygen. Many experimental methods have been employed to study this complex, including a variety of spectroscopic methods. The complexity of the surrounding protein environment challenges reliable interpretation of the spectral features and discrimination between changes in the complex and the many cofactors of photosystem II. We have proposed coherent multidimensional spectroscopy in the mixed time-/frequency-domain as a strategy for exploring the spectroscopy of this important system. Coherent multidimensional spectroscopy is performed by the temporal synchronization and spatial overlap of a sequence of fields to induce a polarization in the material. The fields induced by polarizations meeting certain energy- and momentum-criteria are sampled; the intensity of the fields as functions of frequency and time elucidate the spectral and temporal characteristics of the sample's quantum states. Here, we describe efforts to extend the spectroscopy of model transition metal complexes to the femtosecond regime. We present the implementation of white-light transient absorption and demonstrate our ability to reproduce the spectroscopic behavior of manganese (III) tetraphenylporphine with improved time resolution over previously published results; we discuss the limitations encountered when extending this spectroscopy to homodyne-detected transient grating methods. We have implemented a strategy for broadband coherent anti-Stokes Raman spectroscopy, showing the results of these efforts. A theoretical background into the pulse propagation effects in the ultrafast regime of femtosecond spectroscopy has been compiled. We have found these propagation effects to have profound importance in the tuning and amplification of femtosecond pulses, and we present the results of simulations exploring how these effects manifest and influence the behavior of a particular process employed in light generation in a commercial traveling-wave optical parametric amplifier.
机译:光系统II的放氧配合物是四锰配合物,可催化水氧化成双氧。已经采用了许多实验方法来研究这种复合物,包括各种光谱方法。周围蛋白质环境的复杂性挑战光谱特征的可靠解释以及光系统II的复杂因素和许多辅助因素之间的区别。我们已经提出了时域/频域混合的相干多维光谱作为探索这一重要系统光谱的策略。相干多维光谱通过一系列场的时间同步和空间重叠来执行,以在材料中引起极化。满足特定能量和动量标准的极化引起的磁场被采样。场强作为频率和时间的函数阐明了样品量子态的光谱和时间特性。在这里,我们描述了将模型过渡金属配合物的光谱扩展到飞秒范围的工作。我们介绍了白光瞬态吸收的实现,并证明了我们能够再现锰(III)四苯基卟啉的光谱行为,并具有比先前发表的结果更高的时间分辨率;我们讨论了将此光谱扩展到零差检测瞬态光栅方法时遇到的局限性。我们已经实施了宽带相干反斯托克斯拉曼光谱的策略,显示了这些努力的结果。飞秒光谱的超快状态下脉冲传播效应的理论背景已经被汇编。我们发现这些传播效应在飞秒脉冲的调谐和放大中具有极其重要的意义,并且我们给出了模拟结果,以探索这些效应如何体现和影响商用行波光学系统中光产生中使用的特定过程的行为。参数放大器。

著录项

  • 作者

    Hebert, Paul C.;

  • 作者单位

    The University of Wisconsin - Madison.;

  • 授予单位 The University of Wisconsin - Madison.;
  • 学科 Chemistry.
  • 学位 Ph.D.
  • 年度 2016
  • 页码 406 p.
  • 总页数 406
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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