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In this article we show that linear nanoantennas can be used as shared substrates for surface-enhanced Raman and infrared spectroscopy (SERS and SEIRS, respectively). This is done by engineering the plasmonic properties of the nanoantennas, so to make them resonant in both the visible (transversal resonance) and the infrared (longitudinal resonance), and by rotating the excitation field polarization to selectively take advantage of each resonance and achieve SERS and SEIRS on the same nanoantennas. As a proof of concept, we have fabricated gold nanoantennas by electron beam lithography on calcium difluoride (1-2 μm long, 60 nm wide, 60 nm high) that exhibit a transverse plasmonic resonance in the visible (640 nm) and a particularly strong longitudinal dipolar resonance in the infrared (tunable in the 1280-3100 cm(-1) energy range as a function of the length). SERS and SEIRS detection of methylene blue molecules adsorbed on the nanoantenna's surface is accomplished, with signal enhancement factors of 5×10(2) for SERS (electromagnetic enhancement) and up to 10(5) for SEIRS. Notably, we find that the field enhancement provided by the transverse resonance is sufficient to achieve SERS from single nanoantennas. Furthermore, we show that by properly tuning the nanoantenna length the signals of a multitude of vibrational modes can be enhanced with SEIRS. This simple concept of plasmonic nanosensor is highly suitable for integration on lab-on-a-chip schemes for label-free chemical and biomolecular identification with optimized performances.

Here we report on the complex nature of the phase diagram of N-alkyl-N-methylpiperidinium bis(trifluoromethanesulfonyl)imide ionic liquids using several complementary techniques and on their structural order in the molten state using small-wide angle x-ray scattering. The latter study indicates that the piperidinium aliphatic alkyl chains tend to aggregate, forming alkyl domains embedded into polar regions, similar to what we recently highlighted in the case of other ionic liquids.

Fourier-transform infrared and Raman spectroscopies have been used to investigate the role played by water on the structural organization of 1-butyl-3-methyl-imidazolium tetrafluoroborate and H 2 O mixtures, over a wide composition range at room temperature. Our measurements provide clear experimental evidence of the prompt association between 'free' water molecules and anions at very small water contents. Moreover, in the case of higher water contents, we obtain indications of the local aggregation of water molecules in the network. Such an aggregation is found to occur even before the saturation of all the anions that are available for H-bonding. We propose that the water clusters favour the organization of ionic liquid in the polar network, where they are embedded, and the aggregation of hydrophobic alkyl tails in a micelle-like structure. When mixtures with water molar fraction exceeding 0.7 are considered, this local organization starts to weaken owing to the gradual break up of the ion-pair interactions.

Strategies for in-liquid molecular detection via Surface Enhanced Raman Scattering (SERS) are currently based on chemically-driven aggregation or optical trapping of metal nanoparticles in presence of the target molecules. Such strategies allow the formation of SERS-active clusters that efficiently embed the molecule at the “hot spots” of the nanoparticles and enhance its Raman scattering by orders of magnitude. Here we report on a novel scheme that exploits the radiation pressure to locally push gold nanorods and induce their aggregation in buffered solutions of biomolecules, achieving biomolecular SERS detection at almost neutral pH. The sensor is applied to detect non-resonant amino acids and proteins, namely Phenylalanine (Phe), Bovine Serum Albumin (BSA) and Lysozyme (Lys), reaching detection limits in the μg/mL range. Being a chemical free and contactless technique, our methodology is easy to implement, fast to operate, needs small sample volumes and has potential for integration in microfluidic circuits for biomarkers detection.

We explore the effect of re-radiation in surface-enhanced Raman scattering (SERS) through polarization-sensitive experiments on self-organized gold nanowires on which randomly oriented Methylene Blue molecules are adsorbed. We provide the exact laws ruling the polarized, unpolarized, and parallel- and cross-polarized SERS intensity as a function of the field polarizations. We show that SERS is polarized along the wire-to-wire nanocavity axis, independently from the excitation polarization. This proves the selective enhancement of the Raman dipole component parallel to the nanocavity at the single molecule level. Introducing a field enhancement tensor to account for the anisotropic polarization response of the nanowires, we work out a model that correctly predicts the experimental results for any excitation/detection polarization and goes beyond the E(4) approximation. We also show how polarization-sensitive SERS experiments permit one to evaluate independently the excitation and the re-radiation enhancement factors accessing the orientation-averaged non-diagonal components of the molecular Raman polarizability tensor.

A novel synthesis route driving redox-precipitation reactions among MnVII, CeIII, and MnII precursors in basic aqueous solution yields MnCeO x catalysts (Mnat/Ceat, 0.33−2.0) with a (quasi)molecular dispersion of the active phase and enhanced textural properties in comparison to the conventional coprecipitation method. The basic characteristics of the redox-precipitation process leading to a solid architecture missing a substantial “long-range” crystalline order are discussed. With an excellent reproducibility and irrespective of the Mnat/Ceat ratio, the redox-precipitation method also ensures unchanged textural, structural, and chemical properties of the MnCeO x catalysts. As a much improved dispersion of the active phase, the redox-precipitation route greatly promotes the redox behavior and the surface affinity toward gas-phase oxygen of the MnCeO x system.

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