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Rolf Breinbauer

Publications and source records attributed to Rolf Breinbauer.

2 recordsLinked to original sources

Automated Spin-Assisted Layer-by-Layer Epitaxy Produces Highly Oriented Mixed-Linker MOF Thin Films

Control over crystallographic orientation in metal-organic framework (MOF) thin films is crucial for exploiting their anisotropic properties in sensing, catalysis, and separation. Achieving reproducible, highly oriented films remains challenging, especially for mixed-linker, pillared-layered frameworks. Here we present an automated, spin-assisted layer-by-layer liquid-phase epitaxy (LbL-LPE) strategy that enables rapid, ambient-condition fabrication of highly oriented, mixed-linker MOF thin films, demonstrated for Zn2BDC2DABCO (BDC = terephthalate, DABCO = 1,4-diazabicyclo[2.2.2]octane). Correlative process monitoring by grazing-incidence wide-angle X-ray scattering (GIWAXS), grazing-angle infrared (GI-IR) and UV-Vis spectroscopy, contact-angle measurements, scanning electron microscopy (SEM), and time-of-flight secondary ion mass spectrometry (ToF-SIMS) ensure formation of uniform films with exceptional out-of-plane (001) orientation (degree of orientation >85%, Hermans parameter ~0.95) and excellent reproducibility. This strategy enables highly reproducible, high-throughput fabrication of orientation-controlled MOF thin films, providing a generalizable alternative to conventional LbL approaches. By enabling reproducible and entirely automated fabrication of highly anisotropic architectures, this work establishes a platform for integrating oriented MOFs into next-generation optoelectronic, sensing, and membrane devices where directional transport and ordered pore alignment are essential.

cond-mat.mtrl-sci

Ultra-resolution photochemical sensing

Photochemistry in the earth's atmosphere is driven by the sun, continuously altering the concentration and spatial distribution of pollutants. Precisely monitoring their atmospheric abundance relies predominantly on optical sensing, which requires the knowledge of exact absorption cross sections. One key pollutant which impacts many photochemical reaction-pathways is formaldehyde. Agreement on formaldehyde absolute absorption cross section remains elusive in the photochemically-relevant ultraviolet spectral region, hampering sensitive concentration tracking. Here, we introduce free-running ultraviolet dual comb spectroscopy, combining high spectral resolution (1 GHz), broad spectral coverage (12 THz), and fast acquisition speed (500 ms), as a novel method for absolute absorption cross section determination with unprecedented fidelity. Within this bandwidth, our method uncovers almost one order of magnitude more rovibrational transitions than detected before which leads to refined rotational constants for high-level quantum simulations of molecular eigenstates. This ultra-resolution method can be generalized to provide a universal tool for fast electronic fingerprinting of atmospherically-relevant species, both for sensing applications and to benchmark improvements of ab-initio quantum theory.

physics.optics