SearcharxivSearch

arXiv subjects

Sumea Klokic

Publications and source records attributed to Sumea Klokic.

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

Multi-wavelength transparent microfluidics for UV-visible spectroscopy and X-ray scattering studies of photoactive systems

Microfluidic devices are increasingly used in synchrotron-based experiments to deliver and probe liquid samples, offering advantages such as minimal sample consumption and reduced radiation damage. Despite their growing use, few devices have been specifically designed for monitoring liquids under photoexcitation, a promising approach for fast structural transitions. Here, a microfluidic device that is transparent to X-rays in one direction, and simulaneously transmits UV and visible light in the perpendicular direction is presented. The device is fabricated using lamination and UV lithography on a dry-film resist, eliminating the need for cleanroom facilities and simplifying production. Its multi-wavelength transparency was validated through UV-visible spectroscopy, where photoexcitation at different wavelengths induced reversible trans-to-cis isomerization of azobenzene and fluoro-azobenzene. X-ray transparency was validated through Small Angle X-ray Scattering (SAXS) measurements on hemoglobin and CO-ligated hemoglobin sensitive to quaternary structural changes. These resusts confirm the suitability of the device for resolving protein structures and photoinduced conformational dynamics. The design further supports, as some proof of concept results show, temperature-jump and time resolved pump-probe experiments, providing a versatile platform for studying structural evolution in liquid samples using synchrotron SAXS.

physics.app-ph