arXiv subjects

M. Dürr

Publications and source records attributed to M. Dürr.

5 recordsLinked to original sources

arXiv2026

Demonstrating CBM Capabilities by $Λ$ Baryon Reconstruction in Ni+Ni Collisions with the mCBM Experiment at SIS18 of GSI/FAIR

The Compressed Baryonic Matter (CBM) experiment at the upcoming Facility for Antiproton and Ion Research (FAIR) is a high-rate fixed-target experiment designed to investigate nuclear matter at extreme baryon densities in relativistic nucleus-nucleus collisions. To enable high-statistics measurements of rare probes, CBM is designed to operate at event rates up to 10 MHz. This necessitates the development of fast and radiation-tolerant detectors, self-triggered front-end electronics, a free-streaming data acquisition architecture, and real-time event reconstruction capabilities. Prototype versions and pre-series productions of the CBM detector systems have been deployed in the mini-CBM demonstrator setup mCBM - an experimental precursor comprising sub-components of all major CBM systems, installed at the SIS18 facility of GSI/FAIR within the FAIR Phase-0 program. In 2024, Ni+Ni collisions at a kinetic beam energy of 1.93 AGeV and an average interaction rate of about 250 kHz were successfully recorded. This dataset enables a detailed evaluation of the operational performance of the detector systems as well as the complete CBM data chain, while the reconstruction of rare $Λ$ baryons serves as a natural benchmark. This paper presents the first results on $Λ$ signal reconstruction with the mCBM experiment, demonstrating the readiness of the detector technologies and the data chain for the upcoming full-scale CBM experiment.

physics.ins-det↗

arXiv2021

Tip-Induced $β$-Hydrogen Dissociation in an Alkyl Group Bound on Si(001)

Atomic-scale chemical modification of surface-adsorbed ethyl groups on Si(001) was induced and studied by means of scanning tunneling microscopy. Tunneling at sample bias > +1.5V leads to tip-induced C-H cleavage of a $β$-hydrogen of the covalently bound ethyl configuration. The reaction is characterized by the formation of an additional Si-H and a Si-C bond. The reaction probability shows a linear dependence on the tunneling current at 300 K; the reaction is largely suppressed at 50 K. The observed tip-induced surface reaction at room temperature is thus attributed to a one-electron excitation in combination with thermal activation.

cond-mat.mtrl-sci↗

arXiv2020

Solution-based alkyne-azide coupling on functionalized Si(001) prepared under UHV conditions

Synthesis of organic bi-layers on silicon was realized by a combination of surface functionalization under ultra-high vacuum (UHV) conditions and solution-based click chemistry. The silicon (001) surface was prepared with a high degree of perfection in UHV and functionalized via chemoselective adsorption of ethinyl cyclopropyl cyclooctyne from the gas phase. A second organic layer was then coupled in acetonitrile via the copper-catalyzed alkyne azide click reaction. The samples were directly transferred from UHV via the vapour phase of the solvent into the solution of reactants and back to UHV without contact to ambient conditions. Each reaction step was monitored by means of X-ray photoelectron spectroscopy in UHV; the N 1s spectra clearly indicated the click reaction of the azide group in the two test molecules employed, i.e., methyl-subsituted benzylazide and azide substituted pyrene. In both cases, up to 50 - 60 % of the ethinyl cyclopropyl cyclooctyne molecules on the surface were reacted.

cond-mat.mtrl-sci↗

arXiv2020

Click chemistry in ultra-high vacuum - tetrazine coupling with methyl enol ether covalently linked to Si(001)

The additive-free tetrazine/enol ether click reaction was performed in ultra-high vacuum (UHV) with an enol ether group covalently linked to a silicon surface: Dimethyl 1,2,4,5-tetrazine-3,6-dicarboxylate molecules were coupled to the enol ether group of a functionalized cyclooctyne which was adsorbed on the silicon (001) surface via the strained triple bond of cyclooctyne. The reaction was observed at a surface temperature of 380 K by means of X-ray photoelectron spectroscopy (XPS). No indications for tetrazine molecules which bind directly to the Si(001) surface via the nitrogen atoms were detected. A moderate energy barrier was deduced for this click reaction in vacuum by means of density functional theory based calculations, in good agreement with the experimental results. This UHV-compatible click reaction thus opens a new, flexible route for synthesizing covalently bound organic architectures.

cond-mat.mtrl-sci↗

arXiv2018

Second-harmonic generation as probe for structural and electronic properties of buried GaP/Si(001) interfaces

Optical second-harmonic generation is demonstrated to be a sensitive probe of the buried interface between the lattice matched semiconductors gallium phosphide and silicon with (001) orientation. Rotational anisotropy measurements of SHG from GaP/Si show a strong isotropic component of the response not present for pure Si(001) or GaP(001). The strength of the overlaying anisotropic response directly correlates with the quality of the interface as determined by atomically resolved scanning transmission electron microscopy.Optical second-harmonic generation is demonstrated to be a sensitive probe of the buried interface between the lattice matched semiconductors gallium phosphide and silicon with (001) orientation. Rotational anisotropy measurements of SHG from GaP/Si show a strong isotropic component of the response not present for pure Si(001) or GaP(001). The strength of the overlaying anisotropic response directly correlates with the quality of the interface as determined by atomically resolved scanning transmission electron microscopy. Systematic comparison of samples fabricated with different growth modes in metal organic vapor phase epitaxy reveals that the anisotropy for different polarization combinations can be used as a selective fingerprint for the occurrence of anti-phase domains and twins. This all-optical technique can be applied as an {\it in-situ} and non-invasive monitor even during growth. Systematic comparison of samples fabricated with different growth modes in metal organic vapor phase epitaxy reveals that the anisotropy for different polarization combinations can be used as a selective fingerprint for the occurrence of anti-phase domains and twins. This all-optical technique can be applied as an {\it in-situ} and non-invasive monitor even during growth.

cond-mat.mes-hall↗