Is this you? As a journalist, you can create a free Muck Rack account to customize your profile, list your contact preferences, and upload a portfolio of your best work.
Claim your profile
Articles by Florian Trinter
Generative modeling enables molecular structure retrieval from Coulomb explosion imaging - Nature Communications
Abstract Capturing the structural changes that molecules undergo during chemical reactions in real space and time is a long-standing dream and an essential prerequisite for understanding and ultimately controlling femtochemistry. A key approach to tackle this challenging task is Coulomb explosion imaging, which has benefited decisively from recently emerging high-repetition-rate X-ray free-electron laser sources.
Tracking the Complex Dynamics of Electron-Transfer-Mediated Decay in Real Space and Time
I. Introduction Click to copy section linkSection link copied! In the late 20th century, Cederbaum et al. found that in loosely bound matter efficient nonlocal electronic decay processes can occur. In their work, they identified a general mechanism in which the energy freed by the electronic de-excitation of one molecule of a weakly bound cluster is transferred to a neighboring molecule, triggering its ionization. They termed this process interatomic Coulombic decay (ICD).
Tracking the Complex Dynamics of Electron-Transfer-Mediated Decay in Real Space and Time
Journal of the American Chemical Society Cite this: J. Am. Chem. Soc. 2026, XXXX, XXX Click to copy citationCitation copied! . This publication is licensed under CC-BY 4.0 . You are free to share (copy and redistribute) this article in any medium or format and to adapt (remix, transform, and build upon) the material for any purpose, even commercially within the parameters below: Creative Commons (CC): This is a Creative Commons license. Attribution (BY): Credit must be given to the creator.
Non-local X-ray intermolecular radiative decay probes solvation shell of ions in water - Nature Communications
Abstract Aqueous solutions are crucial in chemistry, biology, environmental science, and technology. The chemistry of solutes is influenced by the surrounding solvation shell of water molecules, which have different chemical properties than bulk water due to their different electronic and geometric structure. It is experimentally challenging to selectively investigate this property-determining electronic and geometric structure.
Imaging a light-induced molecular elimination reaction with an X-ray free-electron laser - Nature Communications
|
Abstract Tracking the motion of individual atoms during chemical reactions represents a severe experimental challenge, especially if several competing reaction pathways exist or if the reaction is governed by the correlated motion of more than two molecular constituents.
By Xiang Li, Rebecca Boll, Patricia Vindel-Zandbergen, Jesus Gonzalez-Vazquez, Daniel Rivas, Keyu Chen, Benjamin Erk, Alice Green, Markus Ilchen, Edwin Kukk, Tommaso Mazza, Terence Mullins, Björn Senfftleben, Florian Trinter, Sergey Usenko, Anbu Selvam Venkatachalam, Enliang Wang, James Cryan, Michael Meyer, Till Jahnke, Phay J. Ho, Daniel Rolles
|
Nature
Verified
Site- and Energy-Selective Low-Energy Electron Emission by X-rays in the Aqueous Phase
Introduction Click to copy section linkSection link copied! A major challenge in X-ray-based radiation therapies is to achieve the largest possible contrast between the doses of radiation deposited in the malignant versus the surrounding healthy tissue, which the radiation inevitably needs to pass through.
Site- and Energy-Selective Low-Energy Electron Emission by X-rays in the Aqueous Phase
Introduction Click to copy section linkSection link copied! A major challenge in X-ray-based radiation therapies is to achieve the largest possible contrast between the doses of radiation deposited in the malignant versus the surrounding healthy tissue, which the radiation inevitably needs to pass through.
Low-Energy Photoelectron Spectroscopy and Scattering from Aqueous Solutions and the Role of Solute Surface Activity
Introduction Click to copy section linkSection link copied! Differential valence-electron energetics in aqueous solutions provide the driving forces for a broad range of (bio)chemical and environmental processes. The accurate measurement of electron binding energies (BEs) of solutes and solvents – which reveal such electron energetics and are directly accessed using liquid-jet photoemission spectroscopy (LJ-PES) (1,2) – is correspondingly crucial.
Low-Energy Photoelectron Spectroscopy and Scattering from Aqueous Solutions and the Role of Solute Surface Activity
Introduction Click to copy section linkSection link copied! Differential valence-electron energetics in aqueous solutions provide the driving forces for a broad range of (bio)chemical and environmental processes. The accurate measurement of electron binding energies (BEs) of solutes and solvents – which reveal such electron energetics and are directly accessed using liquid-jet photoemission spectroscopy (LJ-PES) (1,2) – is correspondingly crucial.
Photoelectron circular dichroism of aqueous-phase alanine
Photoelectron circular dichroism of aqueous-phase alanine† Amino acids and other small chiral molecules play key roles in biochemistry. However, in order to understand how these molecules behave in vivo, it is necessary to study them under aqueous-phase conditions. Photoelectron circular dichroism (PECD) has emerged as an extremely sensitive probe of chiral molecules, but its suitability for application to aqueous solutions had not yet been proven.
Direct observation of ultrafast symmetry reduction during internal conversion of 2-thiouracil using Coulomb explosion imaging - Nature Communications
Abstract The photochemistry of heterocyclic molecules plays a decisive role for processes and applications like DNA photo-protection from UV damage and organic photocatalysis. The photochemical reactivity of heterocycles is determined by the redistribution of photoenergy into electronic and nuclear degrees of freedom, initially involving ultrafast internal conversion. Most heterocycles are planar in their ground state and internal conversion requires symmetry breaking.
Direct observation of the complex S(IV) equilibria at the liquid-vapor interface - Nature Communications
Abstract The multi-phase oxidation of S(IV) plays a crucial role in the atmosphere, leading to the formation of haze and severe pollution episodes. We here contribute to its understanding on a molecular level by reporting experimentally determined pKa values of the various S(IV) tautomers and reaction barriers for SO2 formation pathways.
The solvation shell probed by resonant intermolecular Coulombic decay - Nature Communications
Abstract Molecules involved in solvation shells have properties differing from those of the bulk solvent, which can in turn affect reactivity. Among key properties of these molecules are their nature and electronic structure. Widely used tools to characterize this type of property are X-ray-based spectroscopies, which, however, usually lack the capability to selectively probe the solvation-shell molecules.
X-ray radiation damage cycle of solvated inorganic ions - Nature Communications
Abstract X-ray-induced damage is one of the key topics in radiation chemistry. Substantial damage is attributed to low-energy electrons and radicals emerging from direct inner-shell photoionization or produced by subsequent processes.
Surface Accumulation and Acid-Base Equilibrium of Phenol at the Liquid-Vapor Interface
Surface Accumulation and Acid-Base Equilibrium of Phenol at the Liquid-Vapor Interface We have investigated the surfactant properties of phenol in aqueous solution as a function of pH and bulk concentration using liquid-jet photoelectron spectroscopy (LJ-PES) and surface tension measurements.
A setup for studies of photoelectron circular dichroism from chiral molecules in aqueous solution
A. General considerations Photoelectron spectroscopy (PES) studies from liquids and particularly from water and aqueous solutions, mostly in conjunction with a liquid microjet,1,21. B. Winter and M. Faubel, Chem. Rev. 106(4), 1176 (2006). https://doi.org/10.1021/cr040381p2. R. Dupuy, C. Richter, B. Winter, G. Meijer, R. Schlögl, and H. Bluhm, J. Chem. Phys. 154(6), 060901 (2021). https://doi.org/10.1063/5.0036178 have contributed tremendously to our current understanding of the aqueous-phase electronic structure.
Ultrafast Temporal Evolution of Interatomic Coulombic Decay in NeKr Dimers
This article is Open Access Please wait while we load your content... Something went wrong. Try again?
Accurate Vertical Ionization Energy and Work Function Determinations of Liquid Water and Aqueous Solutions
This article is Open Access Please wait while we load your content... Something went wrong. Try again?
Enabling time-resolved 2D spatial-coherence measurements using the Fourier-analysis method with an integrated curved-grating beam monitor
Author Affiliations Kai Bagschik,1,* Michael Schneider,2 Jochen Wagner,3 Ralph Buss,3,4 Matthias Riepp,1 Andre Philippi-Kobs,1 Leonard Müller,1,5 Wojciech Roseker,1 Florian Trinter,1,6 Moritz Hoesch,1 Jens Viefhaus,7 Stefan Eisebitt,2 Gerhard Grübel,1,4 Hans Peter Oepen,3,4 and Robert Frömter3,4 1Deutsches Elektronen-Synchrotron (DESY), Notkestraße 85, 22607 Hamburg, Germany 2Max-Born-Institut für Nichtlineare Optik und Kurzzeitspektroskopie, Max-Born-Straße 2a, 12489 Berlin, Germany...
Show More
loading
Actions
Is this you?
As a journalist, you can create a free Muck Rack account to customize your profile, list your contact preferences, and upload a portfolio of your best work.Get in touch with Florian
Contact Florian, search articles and posts on X, monitor coverage, and track replies from one place.
Learn more about Muck Rack