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Dylan A. Sherman

Publications and source records attributed to Dylan A. Sherman.

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Elucidating Guest-Host Mechanisms in ZIF-L for Tuneable Highly Luminescent 2D Materials

3D metal-organic frameworks (MOFs) are well known effective hosts for luminescent guests that improve tuneability, photostability and material fabricability. 2D guest@MOF systems, while less explored, offer competitive advantages over 3D guest@MOF systems due to their optical transparency, inter-layer spacing, and vertical thinness. This work examines luminescent organic dyes@ZIF-L to establish the underlying mechanisms of guest incorporation in ZIF-L and demonstrate the advantages of the 2D ZIF-L architecture for the material's functional luminescence. Analysing a case study system, fluorescein@ZIF-L (F@ZIF-L), using nanoscale FTIR, diffraction, and topology mapping, confirmed that fluorescein (F) resided in the ZIF-L framework cavities. Supported by surface energy simulations, the extent of guest incorporation was found to be indicated by a morphological continuum, from the characteristic leaf-shaped ZIF-L to rectangular F@ZIF-L. By modifying synthesis temperature and solvent ratios, the luminescent properties of F@ZIF-L could be rationally tuned in terms of guest loading (% mol) and arrangement (i.e. guest monomer to aggregate ratio). When optimised, F@ZIF-L exhibited tuneable emission chromaticity, 99.7% photoluminescent quantum yield, minimal guest leaching in solution over 12 months, and high photostability. Perylene@ZIF-L exhibited unique white light emitting properties, with CIE coordinates (0.33, 0.34) arising from a combination of yellow alpha-phase excimer and blue monomeric perylene emission. Finally, oriented luminescent thin films of guest@ZIF-L materials were grown on malleable Zn foils, demonstrating an in situ fabrication technique. Together, the work highlights the potential for luminescent dye@ZIF-L systems in developing tuneable and resilient luminescent components of next-generation optoelectronics, sensors, and lighting systems.

cond-mat.mtrl-sci

Quantifiably Tuneable Luminescence by Ultra-Thin Metal-Organic Nanosheets via Dual-Guest Energy Transfer

Luminescent metal-organic frameworks (LMOFs) are promising materials for organic light-emitting diode (OLED) alternatives to silicate-based LEDs due to their tuneable structure and programmability. Yet, the 3D nature of LMOFs creates challenges for stability, optical transparency, and device integration. Metal-organic nanosheets (MONs) potentially overcome these limitations by combining the benefits of MOFs with an atomically thin morphology of large planar dimensions. Here, we report the bottom-up synthesis of atomically thin ZIF-7-III MONs via facile low-energy salt-templating. Employing guest@MOF design, the fluorophores Rhodamine B and Fluorescein were intercalated into ZIF-7 nanosheets (Z7-NS) to form light emissive systems exhibiting intense and highly photostable fluorescence. Aggregation and Förster resonance energy transfer, enabled by the MON framework, were revealed as the mechanisms behind fluorescence. By varying guest concentration, these mechanisms provided predictable quantified control over emission chromaticity of a dual-guest Z7-NS material and the definition of an 'emission chromaticity fingerprint' - a unique subset of the visible spectrum which a material can emit by fluorescence.

physics.app-ph