Structural characterization and plasmonic properties of manganese oxide-coated gold nanorods.

The preparation of metal@(dielectric or semiconductor) core@shell hybrid materials have been shown promising for both SERS and SEF applications due to improved stability in the presence of ions and the adsorbate compared to non-covered metallic nanoparticles. However, fine control over the thickness of the covering layer is essential to maximize the intrinsic trade-off between the plasmonic enhancement and the chemical stability improvement. Here, the preparation of manganese dioxide ultrathin layers covered gold nanorods (AuNR@MnO2) with varying thicknesses of the MnO2 layer is reported, and the characterization and evaluation of the resulting materials as SERS and SEF substrate. The MnO2 layer over the AuNR was prepared by reducing potassium permanganate by sodium oxalate in a basic medium. The AuNR@MnO2 hybrid material was characterized by UV-Vis spectroscopy, transmission electron microscopy, X-ray powder diffraction, and cyclic voltammetry. It was studied the SEF effect of the cyanine dye IR-820 excited at 785 nm with high performance for several thicknesses of the MnO2 ultrathin film. The enhancement factor increased for thicker oxide layers. The SERS effect of the IR-820 dye excited at 633 nm showed the most significant enhancement factor for thinner layers. The seemly opposite behavior of the two plasmonic effects may be assigned to the distance dependence of the electromagnetic field generated in the AuNR, which results in decreasing SERS performance. For SEF, the thinner layers resulted in the Au nanoparticles' emission quenching, so a more significant distance was necessary to observe enhancement.

Impact of nanoconfinement on acetylacetone Equilibria in Ordered Mesoporous Silicates.

Nanoconfinement is one of the most intriguing nanoscale effects and affects several physical and chemical properties of molecules and materials, including viscosity, reaction kinetics, and glass transition temperature. In this work, liquid nuclear magnetic resonance (NMR) was used to analyze the behavior of 2,4-pentadienone in ordered mesoporous materials with a pore diameter of between 3 and 10 nm. The liquid NMR results showed meaningful changes in the hydrogen chemical shift and the keto-enol chemical equilibrium, which were associated with the pore diameter, allowing the authors to observe the effects of nanoconfinement. An interesting phenomenon was observed where the chemical equilibria of 2,4-pentadienone confined in a mesoporous material with a pore diameter of 3.5 nm was similar to that obtained with free (bulk) 2,4-pentadienone in larger pore materials. Another interesting result was observed for the enthalpy and entropy of the tautomeric equilibria of 2,4-pentadienone confined in mesoporous materials with a 5.5 nm pore diameter being -7.9 kJ mol-1 and -15.9 J mol-1.K. These values are similar to those obtained by dimethyl sulfoxide. This phenomenon indicates the possible use of ordered mesoporous materials as a reaction substitute in organic solvents. It was further observed that while the values of enthalpy (ΔH) and entropy (ΔS) had been modified by confinement, the Gibbs free energy (ΔG) value remained closer to that observed in free (bulk) 2,4-pentadienone. It is expected that this study will help in understanding the effects of nanoconfinement and provide a simple method to employ NMR techniques to analyze these phenomena.