Showing posts with label Thomas Elsaesser. Show all posts
Showing posts with label Thomas Elsaesser. Show all posts

Sunday, September 10, 2017

Abstract-Strong Local-Field Enhancement of the Nonlinear Soft-Mode Response in a Molecular Crystal


Giulia Folpini, Klaus Reimann, Michael Woerner, Thomas Elsaesser, Johannes Hoja,  Alexandre Tkatchenko,

https://journals.aps.org/prl/abstract/10.1103/PhysRevLett.119.097404


The nonlinear response of soft-mode excitations in polycrystalline acetylsalicylic acid (aspirin) is studied with two-dimensional terahertz spectroscopy. We demonstrate that the correlation of CH3rotational modes with collective oscillations of π electrons drives the system into the nonperturbative regime of light-matter interaction, even for a moderate strength of the THz driving field on the order of 50kV/cm. Nonlinear absorption around 1.1 THz leads to a blueshifted coherent emission at 1.7 THz, revealing the dynamic breakup of the strong electron-phonon correlations. The observed behavior is reproduced by theoretical calculations including dynamic local-field correlations.
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Sunday, August 6, 2017

Abstract-Strong local-field enhancement of the nonlinear softmode response in a molecular crystal


Giulia Folpini, Klaus Reimann, Michael Woerner, Thomas Elsaesser, Johannes Hoja, and Alexandre Tkatchenko

https://journals.aps.org/prl/accepted/ae076Yc0Mb51db56829d2d3865649318b071feee8

The nonlinear response of softmode excitations in polycrystalline acetylsalicylic acid (aspirin) is studied with two-dimensional terahertz spectroscopy. We demonstrate that the correlation of CH3 rotational modes with collective oscillations of \pi electrons drives the system into the nonperturbative regime of light-matter interaction, even for a moderate strength of the THz driving field on the order of 50~kV/cm. Nonlinear absorption around 1.1~THz leads to a blueshifted coherent emission at 1.7~THz, revealing the dynamic breakup of the strong electron-phonon correlations. The observed behavior is reproduced by theoretical calculations including dynamic local-field correlations.

Friday, May 13, 2016

Abstract-Phase-resolved two-dimensional terahertz spectroscopy including off-resonant interactions beyond the χ(3) limit


http://scitation.aip.org/content/aip/journal/jcp/144/18/10.1063/1.4948639

We present the first two-dimensional (2D) terahertz (THz) experiment with three phase-locked THz pulses and a fully phase-resolved detection of the nonlinearly emitted field by electrooptic sampling. In a prototype experiment we study the ultrafast dynamics of nonlinear two-phonon and two-photon interbandcoherences in the narrow-gap semiconductor InSb. Due to the extraordinarily large optical interband dipole of InSb the experiments were performed in the strongly nonperturbative regime of light-matter interaction allowing for impulsive off-resonant excitation of both two-phonon coherences and two-photoninterband coherences, the ultrafast dynamics of which is experimentally observed as a function of the waiting time in the three-pulse 2D experiment. Our novel three-pulse 2D THz spectroscopy paves the way for the detailed investigation of nonlinear quantum coherences in solids and holds potential for an extension to other systems.

Tuesday, December 15, 2015

Isolating water's impact on vibrations within DNA


http://phys.org/news/2015-12-isolating-impact-vibrations-dna.html

In a biological system, the ratio of water-to-non-water molecules, known as the hydration level, influences both the arrangement of biomolecules and the strength of the electric interactions that occur between biomolecules, free ions, and functional groups, which are groups of atoms within molecules that strongly influence the molecules' chemical properties. To isolate the contribution of water to the vibrational fluctuations that occur between DNA, bulk water, and the charged biomolecular interface between the two, researchers at the Max-Born Institute for Nonlinear Optics and Short Pulse Spectroscopy in Berlin have performed two-dimensional spectroscopic analyses on double-stranded DNA helices at different hydration levels.

The analysis gives insight into the way  and DNA interact, which could ultimately help scientists understand how biological systems function at the molecular level and what goes wrong when adverse conditions cause the systems to fail.

Two-dimensional infrared spectroscopy is a laser technique used to map correlated vibrations, the basic oscillatory motions of atoms, and their fluctuations into observable data.
The researchers used an amplified titanium-sapphire laser system to generate a sequence of four femtosecond infrared pulses in the low-frequency range that corresponds to the vibrational modes of DNA's sugar-phosphate backbones between 920 and 1120 cm-1. They found that the spectra give evidence of both ultrafast structural fluctuations and a broadening of vibrational transitions, which reflects the structural disorder and variation of hydrogen bonding at the DNA-water interface.
"We were looking for probes which are most sensitive to dynamics at the [DNA-water] interface and noninvasive, leaving the structure of the interface unchanged," said Thomas Elsaesser, director of the institute and a professor of experimental physics at Humboldt University of Berlin. "We concluded that [DNA] backbone modes would be interesting candidates, as their elongations are at the interface and they should be sensitive to local electric fields."
Elsaesser and his colleagues at the Max-Born Institute detail their investigations this week in Structural Dynamics.
Their current work builds on a seminal paper published in Nature in 2005 - with the collaboration of Dwayne Miller's group at the University of Toronto - which reported the first two-dimensional spectra of bulk water and established the basic time scales of the structural fluctuations that determine the lineshapes of vibrations.
For DNA, dehydration induces a transition from the traditional B-helix form to the A-helix form, the second most common shape. To determine the vibrational contribution of a system's hydration level, Elsaesser and his colleagues spectroscopically examined DNA strands at 0% humidity and 92% humidity, which correspond to around 2 and 20 water molecules per base pair, respectively.
By analyzing the two-dimensional spectral lineshapes, the researchers found that the hydrated DNA strands display structural fluctuations on a sub-picosecond time scale - less than a trillionth of a second - and that the structural disorder of local arrangements of water and DNA functional groups persists for time scales longer than 10 picoseconds, leaving water-DNA hydrogen bonds intact. Additionally, they found that although the arrangement of interfacial water molecules fluctuates at a slower rate compared to bulk water, it makes a substantial contribution to the sub-picosecond fluctuations, along with the low-frequency motions of the DNA helix.
They also noticed a pronounced coupling of the different, partly delocalized backbone modes. According to Elsaesser, this results in an energy transfer between the modes on a time scale of a few picoseconds.
Future work for Elsaesser and his colleagues includes extending their investigation toward longer natural DNA and RNA systems, such as DNA from salmon testes in a full water environment, as well as investigating the terahertz spectroscopy of low frequency motions and electric interactions.
More information: Biswajit Guchhait et al. Ultrafast vibrational dynamics of the DNA backbone at different hydration levels mapped by two-dimensional infrared spectroscopy, Structural Dynamics (2016). DOI: 10.1063/1.4936567


Sunday, July 12, 2015

Abstract-Ultra-broadband terahertz pulses generated in the organic crystal DSTMS



Carmine Somma, Giulia Folpini, Jyotsana Gupta, Klaus Reimann, Michael Woerner, and Thomas Elsaesser
https://www.osapublishing.org/ol/abstract.cfm?uri=ol-40-14-3404#Abstract

Electric-field transients covering the extremely wide frequency range from 0.5 to 26 THz are generated in the organic nonlinear crystal 4-N,N-dimethylamino-4-N-methylstilbazolium 2,4,6-trimethylbenzenesulfonate (DSTMS). Parametric difference frequency mixing within the spectrum of 25-fs amplified pulses centered at 800 nm provides a highly stable broadband output with an electric-field amplitude of up to several hundred kilovolts/cm. The high stability of the terahertz pulse parameters allows for sensitive phase-resolved broadband spectroscopy of optically thick crystalline samples.
© 2015 Optical Society of America
Full Article  |  PDF Article

Tuesday, March 5, 2013

Abstract-Ultrafast two-dimensional terahertz spectroscopy of elementary excitations in solids



Michael Woerner, Wilhelm Kuehn, Pamela Bowlan, Klaus Reimann and Thomas Elsaesser
http://iopscience.iop.org/1367-2630/15/2/025039

Recent experimental progress has allowed for the implementation of nonlinear two-dimensional (2D) terahertz (THz) spectroscopy in the ultrafast time domain. We discuss the principles of this technique based on multiple phase-locked electric field transients interacting in a collinear geometry with a solid and the phase-resolved detection of the THz fields after interaction with the sample. To illustrate the potential of this new method, 2D correlation spectra of coupled intersubband-longitudinal optical phonon excitations in a double quantum well system and a study of ultrafast carrier dynamics in graphene are presented.