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Multidimensional X-Ray Spectroscopy of Valence and Core Excitations in Cysteine

TLDR
The coupling between valence- and core-excited states can be visualized in three-dimensional plots, revealing the origin of the polarizability that controls the simpler pump-probe SXRS signals.
Abstract
Several nonlinear spectroscopy experiments which employ broadband x-ray pulses to probe the coupling between localized core and delocalized valence excitation are simulated for the amino acid cysteine at the K-edges of oxygen and nitrogen and the K and L-edges of sulfur. We focus on two dimensional (2D) and 3D signals generated by two- and three-pulse stimulated x-ray Raman spectroscopy (SXRS) with frequency-dispersed probe. We show how the four-pulse x-ray signals $\boldsymbol{k}_\mathrm{I}=-\boldsymbol{k}_1+\boldsymbol{k}_2+\boldsymbol{k}_3$ and $\boldsymbol{k}_\mathrm{II}=\boldsymbol{k}_1-\boldsymbol{k}_2+\boldsymbol{k}_3$ can give new 3D insight into the SXRS signals. The coupling between valence- and core-excited states can be visualized in three dimensional plots, revealing the origin of the polarizability that controls the simpler pump-probe SXRS signals.

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Ab initio calculation of vibrational absorption and circular dichroism spectra using density functional force fields

TL;DR: In this paper, the unpolarized absorption and circular dichroism spectra of the fundamental vibrational transitions of the chiral molecule, 4-methyl-2-oxetanone, are calculated ab initio using DFT, MP2, and SCF methodologies and a 5S4P2D/3S2P (TZ2P) basis set.
Journal ArticleDOI

Recent experimental and theoretical developments in time-resolved X-ray spectroscopies

TL;DR: In this paper, the authors discuss recent experimental and theoretical developments in ultrafast X-ray absorption spectroscopies (XAS) and explore the new opportunities they offer, as well as the driving force for new theoretical methods permitting a detailed interpretation of the spectra in terms of the geometrical and electronic properties of the system.
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Photochemical Processes Revealed by X-ray Transient Absorption Spectroscopy

TL;DR: In this paper, the authors reviewed current achievements and capabilities in chemical dynamics from XTA spectroscopy based mainly on studies by the authors, collaborators, and cousers of the same facility and then outlined some future challenges and impacts in chemical sciences using pulsed X-rays from the third-generation synchrotron and the fourth-generation X-ray free-electron light sources.
Journal ArticleDOI

Watching energy transfer in metalloporphyrin heterodimers using stimulated X-ray Raman spectroscopy

TL;DR: This work shows how ultrafast hard X-ray pulses may be used to create localized electronic wavepackets in a metalloporphyrin dimer by combining the broad bandwidth of attosecond pulses with the localized nature of core orbitals results in a much higher degree of localization and temporal resolution than is possible with optical pulses.
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Multidimensional resonant nonlinear spectroscopy with coherent broadband x-ray pulses

TL;DR: Bennett et al. as mentioned in this paper survey various possible types of multidimensional x-ray spectroscopy techniques and demonstrate the novel information they can provide about molecules, such as core-electronic structure and couplings, real-time tracking of impulsively created valence-electronics wavepackets and electronic coherences, and monitoring ultrafast processes such as nonadiabatic electron-nuclear dynamics near conical-intersection crossings.
References
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Journal ArticleDOI

Probing interactions between core-electron transitions by ultrafast two-dimensional x-ray coherent correlation spectroscopy.

TL;DR: Two-dimensional x-ray correlation spectra obtained by varying two delay periods in a time-resolved coherent all-x-ray four-wave-mixing measurement are simulated for the N 1s and O 1s transitions of aminophenol.
Journal ArticleDOI

Manipulating one- and two-dimensional stimulated-x-ray resonant-Raman signals in molecules by pulse polarizations

TL;DR: In this article, a super magic angle (SMA) combination of two measurements with specific pulse polarization configurations was used to simplify the interpretation of spontaneous (RIXS) and stimulated x-ray Raman scattering (SXRS).
Journal ArticleDOI

Two-color phase-sensitive x-ray pump-probe spectroscopy

TL;DR: X-ray pump-probe spectroscopy is studied theoretically in this paper, where it is shown that two-color-optical+x-ray-excitation with constant phase of the pump radiation exhibits strong interference between the one-colour and one-ray spectra.
Journal Article

Two-color phase-sensitive x-ray pump-probe spectroscopy (9 pages)

F. F. Guimaraes
- 01 Jan 2004 - 
TL;DR: X-ray pump-probe spectroscopy is studied theoretically in this paper, where it is shown that two-color-optical+x-ray-excitation with constant phase of the pump radiation exhibits strong interference between the one-colour and one-ray spectra.
Journal ArticleDOI

Probe of the electron correlation in sequential double ionization of helium by two-color attosecond pulses

TL;DR: In this paper, the authors theoretically study the sequential double ionization of He by two-color attosecond pulses and show that, for short time delays between the two pulses, the ionization spectra cannot be explained by an independent model based on the time-dependent perturbation theory.
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