arXiv subjects

Jonas Tauch

Publications and source records attributed to Jonas Tauch.

3 recordsLinked to original sources

arXiv2026

Pressure-tuning of electronic structure of CeTe3 probed by femtosecond collective mode spectroscopy

We use femtosecond optical spectroscopy to study the evolution of coherent order-parameter dynamics in the prototypical charge-density-wave (CDW) system CeTe3 under hydrostatic pressure. The CDW transition temperature decreases from approximately 570 K at ambient pressure to near room temperature at approximately 6 GPa. The pressure dependence of the order-parameter recovery dynamics indicates enhanced electron-phonon coupling with increasing pressure, implying that CDW suppression is driven predominantly by the reduction in Fermi-surface nesting. Above 7 GPa, no evidence of CDW order is observed down to cryogenic temperatures. Concurrently, the relaxation dynamics exhibit significant slowing down at low-temperatures, consistent with emerging heavy-electron behaviour due to pressure-enhanced hybridization between localized Ce 4f levels and itinerant carriers.

cond-mat.str-el↗

arXiv2022

Laser-induced forced evaporative cooling of molecular anions below 4 Kelvin

The study of cold and controlled molecular ions is pivotal for fundamental research in modern physics and chemistry. Investigations into cooling molecular anions, in particular, have proven to be of key consequence for the production of cold antihydrogen, the creation, and study of anionic Coulomb crystals as well as in atmospheric research and astrochemistry. The commonly used anion cooling technique via collisions with a buffer gas is limited by the temperature of the used cryogenic cooling medium. Here, we demonstrate forced evaporative cooling of anions via a laser beam with photon energies far above the photodetachment threshold of the anion. We reach runaway evaporative cooling of an anionic OH$^{-}$ ensemble from an initial temperature of 370(12) K down to 2.2(8) K. This corresponds to three orders of magnitude increase in the ions' phase space density approaching the near-strong Coulomb coupling regime. A quantitative analysis of the experimental results, via a full thermodynamic model including the role of intrinsic collisional heating, represents the anion cooling dynamics without any fitting parameters. This technique can be used to cool, in principle, any anionic species below liquid helium temperature, providing a novel tool to push the frontiers of anion cooling to much lower than the state-of-the-art temperature regimes.

physics.atom-ph↗

arXiv2022

Associative detachment in anion-atom reactions involving a dipole-bound electron

Associative electronic detachment (AED) between anions and neutral atoms leads to the detachment of the anion's electron resulting in the formation of a neutral molecule. It plays a key role in chemical reaction networks, like the interstellar medium, the Earth's ionosphere and biochemical processes. Here, a class of AED involving a closed-shell anion (OH^-) and alkali atoms (rubidium) is investigated by precisely controlling the fraction of electronically excited rubidium. Reaction with the ground state atom gives rise to a stable intermediate complex with an electron solely bound via dipolar forces. The stability of the complex is governed by the subtle interplay of diabatic and adiabatic couplings into the autodetachment manifold. The measured rate coefficients are in good agreement with ab initio calculations, revealing pronounced steric effects. For excited state rubidium, however, a lower reaction rate is observed, indicating dynamical stabilization processes suppressing the coupling into the autodetachment region. Our work provides a stringent test of ab initio calculations on anion-neutral collisions and constitutes a generic, conceptual framework for understanding electronic state dependent dynamics in AEDs.

physics.chem-ph↗