No abstract

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.