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Yovan de Coene

Publications and source records attributed to Yovan de Coene.

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Characterization of Photopolymerized Microscopic Chiral Structures Using Photonic Orbital Angular Momentum

The controlled fabrication and chiroptical characterization of microscale chiral structures remain central challenges in photonics, sensing, and metamaterial engineering. Here we demonstrate an accessible, low-cost platform that combines digital micromirror device-enabled maskless photolithography with capillarity-induced self-assembly to produce polymer chiral microstructures of deterministic handedness, and a liquid-crystal spatial light modulator to generate vortex beams for their characterization via helical dichroism (HD). Using a standard 532 nm laser, we observe HD signals of approximately 30% for microstructures with a characteristic diameter of about 15 micrometers. Rigorous finite-difference time-domain simulations performed on three-dimensional geometries reconstructed from high-resolution Scanning Electron Microscopy data reproduce the experimental HD spectra and confirm the role of structural handedness in driving the differential orbital angular momentum (OAM) response. Near-mirror-symmetric HD spectra for opposite-handed enantiomers, combined with a vanishing response for achiral controls, establish OAM as a robust and spatially selective chiral probe at the microscale. Crucially, both fabrication and characterization rely on equipment standard in an optics laboratory, without recourse to femtosecond sources, plasmonic substrates, or costly photoresists. These results open practical pathways toward OAM-driven chiral sensing, enantioselective detection, and photonic logic devices.

physics.optics

Amorphous to Crystalline Transformation: How Cluster Aggregation Drives the Multistep Nucleation of ZIF-8

Nucleation, the pivotal first step of crystallization, governs essential characteristics of crystallization products, including size distribution, morphology, and polymorphism. While understanding this process is paramount to the design of chemical, pharmaceutical and industrial production processes, major knowledge gaps remain, especially with respect to the crystallization of porous solids. Also for nanocrystalline ZIF-8, one of the most widely studied metal-organic frameworks, questions regarding the species involved in the nucleation pathway and their structural and chemical transformations remain unanswered. By combining harmonic light scattering, inherently sensitive to structural changes, with NMR spectroscopy, which reveals molecular exchanges between particles and solution, we were able to capture the crystallization mechanism of ZIF-8 in unprecedented detail. This dual approach provides concurrent structural and chemical insights, revealing key processes not previously observed in ZIF crystallization. Upon mixing small charged prenucleation clusters (PNCs) are formed, exhibiting an excess of ligands and net positive charge. We show that nucleation is initiated by aggregation of PNCs, through the release of ligands and associated protons to the liquid. This leads to the formation of charge neutral amorphous precursor particles (APPs) which incorporate neutral monomers from solution, and crystallize ZIF-8. Our work highlights chemical dynamics as a vital, yet often overlooked, dimension in the multi-stage structural evolution of MOFs. By establishing the critical role of PNCs in the nucleation of ZIF-8, new pathways open up for controlling crystallization of metal-organic frameworks through targeted chemical interactions with these species.

cond-mat.mtrl-sci