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Giovanni Birarda

Publications and source records attributed to Giovanni Birarda.

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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

Addressable Graphene Encapsulation of Wet Specimens on a Chip for Combinatorial Optical, Electron, Infrared and X-ray based Spectromicroscopy Studies

Label-free spectromicroscopy methods offer the capability to examine complex cellular phenomena. Electron and X-ray-based spectromicroscopy methods, though powerful, have been hard to implement with hydrated objects due to the vacuum incompatibility of the samples and due to the parasitic signals from (or drastic attenuation by) the liquid matrix surrounding the biological object of interest. Similarly, for many techniques that operate at ambient pressure, such as Fourier Transform Infrared spectromicroscopy (FTIRM), the aqueous environment imposes severe limitations due to the strong absorption by liquid water in the infrared regime. Here we propose a microfabricated multi-compartmental and reusable hydrated sample platform suitable for use with several analytical techniques, which employs the conformal encapsulation of biological specimens by atomically thin graphene. Such an electron, X-ray, and infrared transparent, molecularly impermeable as well as mechanically robust enclosure preserve the hydrated environment around the object for a sufficient time to allow in-situ examination of hydrated bio-objects with techniques operating both in ambient or high vacuum conditions. An additional hydration source, made by hydrogel pads patterned near/around the specimen and co-encapsulated, has been added to further extend the hydration lifetime. Scanning electron and optical fluorescence microscopies, as well as synchrotron radiation-based FTIR and X-ray fluorescence microscopies, have been used to test the applicability of the platform and for its validation with yeast, A549 human carcinoma lung cells and micropatterned gels as biological object phantoms.

physics.ins-det