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Volker Engel

Researcher at University of Würzburg

Publications -  237
Citations -  5956

Volker Engel is an academic researcher from University of Würzburg. The author has contributed to research in topics: Wave packet & Excited state. The author has an hindex of 36, co-authored 227 publications receiving 5568 citations. Previous affiliations of Volker Engel include Heidelberg University.

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Photoluminescence and Conductivity of Self-Assembled π–π Stacks of Perylene Bisimide Dyes

TL;DR: In this article, the self-assembly of perylene bisimide dye 2 into pi stacks, both in solution and condensed phase, has been studied in detail by NMR spectroscopy, vapor pressure osmometry (VPO), UV/Vis and fluorescence analysis, differential scanning calorimetry (DSC), optical polarizing microscopy (OPM) and X-ray diffraction.
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Exciton Trapping in π-Conjugated Materials: A Quantum-Chemistry-Based Protocol Applied to Perylene Bisimide Dye Aggregates

TL;DR: A quantum-chemistry-based protocol that provides quantitative and qualitative insight into fluorescence spectra has been applied to perylene bisimide dimers and provides excellent agreement with measured fluorescence Spectra.
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Intense-Field Double Ionization of Helium: Identifying the Mechanism

TL;DR: It is provided strong evidence that rescattering is responsible for nonsequential ionization by calculating the momentum spectrum of the He2+ recoil ions and by analyzing the electronic center-of-mass motion via Wigner transforms.
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Femtosecond laser photoelectron spectroscopy on atoms and small molecules: prototype studies in quantum control.

TL;DR: At atoms and diatomics under gas-phase collision-free conditions to allow for a comparison between theory and experiment, atomic/molecular beam techniques are combined together with femtosecond laser techniques and energy-resolved photoelectron spectroscopy and ion detection.
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On the geometry dependence of molecular dimer spectra with an application to aggregates of perylene bisimide

TL;DR: In this paper, the spectroscopic properties of molecular dimers coupled by dipole-dipole interactions within the framework of time-dependent quantum mechanics were studied, where a systematic variation of the dimer geometry allows to establish relationships between the latter and structures in the absorption spectrum.