The tuning of the optical properties of pyrene, immobilized on alumina nanoparticle surfaces, is demonstrated. To this end, phosphonic acid functionalized pyrene derivatives are shown to self‐assemble into stoichiometrically mixed monolayers featuring hydrophilic, hydrophobic, or fluorophilic phosphonic acid ligands and to form defined core–shell hybrids depending on the molecular mixing ratio and the nature of the ligand monomer, excimer, or mutual emission of both evolved. The spectroscopic observations are explained by the respective mobility of the dye molecules with respect to their fixed, specific anchor points and the resulting probability to form excimers and are supported by molecular dynamic simulations, X‐ray reflectivity measurements, and temperature‐dependent steady‐state fluorescence assays. In terms of an additional tuning of the emission color change and/or the on‐off switching of the fluorescence, the formation of core–shell–shell system is carried out by applying amphiphiles. The general concept is fully transferable to demobilized films of nanoparticles, thereby enabling a switchable solid‐state surface.

Solid catalysts with ionic liquid layers (SCILLs) are heterogeneous catalysts coated with a thin layer of an ionic liquid (IL) to improve their selectivity. In this study, we investigated the interplay of the room-temperature IL 1-butyl-1-methylpyrrolidinium bis(trifluoromethylsulfonyl)imide [C 4 C 1 Pyr][NTf 2 ] with transition metal surfaces of both Pd(111) single crystals and Pd nanoparticles (NPs) supported on highly oriented pyrolytic graphite (HOPG). To this end, we combine theoretical insights obtained by density functional theory (DFT) and molecular dynamics (MD) calculations with experimental data acquired via time-resolved infrared reflection absorption spectroscopy (TR-IRAS) performed under ultrahigh vacuum (UHV) conditions. IL monolayer films formed on Pd(111) and Pd NPs are strongly bound to the surface via the SO 2 moiety of the [NTf 2 ] − anion. By combination of IRAS, DFT, and MD, we identify the most common adsorption motifs. Most importantly, the binding motif of the anion changes as a function of the IL coverage. On supported Pd NPs, additional effects arise from the particle morphology and from the diffusion of carbon from the support to the Pd NPs. Our results suggest that the effect of the IL film on the catalytic activity should strongly depend on the local coverage and the morphology of the catalyst NPs.

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In this study, the syntheses of edge-functionalized hexa-peri-hexabenzocoronene and investigations by steady-state and time-resolved photospectroscopic techniques, which are completed by electron density distribution calculations, are reported.