Vibrational Sum Frequency Generation Spectroscopy of Surface Hydroxyls on Nickel Phyllosilicate Nanoscrolls.

Phyllosilicate clays are layered structures with diverse nanoscale morphology depending on the composition. Size mismatch between the sheets can cause them to form nanoscrolls, a spiral structure with different inner and outer surface charges. The hydroxyls on the exposed surface of the nanoscrolls determine the adsorption properties and hydrophilicity of the surface. Vibrational sum frequency generation (VSFG) spectroscopy was applied to study the surface hydroxyls of nickel phyllosilicate (Ni3Si2O5(OH)4), revealing three distinct in-phase OH-stretch modes: 3642, 3645, and 3653 cm-1. The relative signs of the peaks allow their assignment as "outward" and "inward" pointing hydroxyls on the opposite sides of the scrolled sheet, consistent with the crystal structure. Orientational analysis of polarization-selected VSFG spectra is consistent with a broad (140-164°) step-function distribution of the OH-stretch tilt angles, which we attribute to the uncompensated portion of the scroll rolled more than a whole number of full turns.

Re-orientation of water molecules in response to surface charge at surfactant interfaces.

We present a measurement of molecular orientation of water at charged surfactant aqueous interfaces as a function of surface charge density. The polarization dependent spectral line shapes of the water bend mode were measured by vibrational sum-frequency generation at the positively charged surfactant cetyltrimethylammonium bromide (CTAB)/water interface and negatively charged surfactant sodium dodecyl sulfate/water interface. Orientational analysis using the water bend mode as a vibrational probe, within the electric dipole approximation, reveals structural differences between these surfaces and quantifies how different hydrogen bonded species re-orient around the surfactant head groups as the surface charge density changes. As the concentration of the positively charged surfactant (CTAB) increases, the surface water molecules with free-OH groups reorient their hydrogen away from the bulk water and the C2v axis closer to the surface normal. This suggests that these free-OH molecules are in general located above the positively charged head groups of CTAB, and thus, the charge-dipole interaction pulls their oxygen "down" and pushes hydrogen "up." On the contrary, water molecules with two donor hydrogen bonds re-orient their hydrogen toward the bulk water, likely because most of these molecules are below the CTAB surfactant head groups.

Molecular Orientation of Poly-3-hexylthiophene at the Buried Interface with Fullerene.

Molecular orientation at the donor-acceptor interface plays a crucial role in determining the efficiency of organic semiconductor materials. We have used vibrational sum frequency generation spectroscopy to determine the orientation of poly-3-hexylthiophene (P3HT) at the planar buried interface with fullerene (C60). The thiophene rings of P3HT have been found to tilt significantly toward C60, making an average angle θ ≈ 49° ± 10° between the plane of the ring and the interface. Such tilt may be attributed to π-π stacking interactions between P3HT and C60 and may facilitate efficient charge transfer between donor and acceptor. Upon annealing, the thiophene rings tilt away from the interface by Δθ = 12-19°. This may be attributed to higher crystallinity of annealed P3HT that propagates all the way to the interface, resulting in more "edge-on" orientation, which is consistent with the observed red-shift by ∼6 cm-1 and spectral narrowing of the C=C stretch bands.

Insight into Water Structure at the Surfactant Surfaces and in Microemulsion Confinement.

Interactions with surfactant molecules can significantly alter the structure of interfacial water. We present a comparative study of water-surfactant interactions using two different spectroscopic approaches: water at planar surfactant monolayers by sum frequency generation (SFG) spectroscopy and interfacial water confined in reverse micelles formed by the same surfactants using IR absorption spectroscopy. We report spectral features in the OH-stretching region (3200-3700 cm-1) that are observed in both IR and SFG spectra, albeit with different relative amplitudes, for ionic surfactant sodium 1,4-bis-2-ethylhexylsulfosuccinate (AOT) and nonionic surfactant polyoxyethylene(4)lauryl ether (Brij L-4) reverse micelles in hexane and the corresponding monolayers at the air/water interface. A prominent feature in the SFG spectra of the OH stretch at 3560 cm-1 is attributed to water molecules that have a weak donor hydrogen bond to the surfactant headgroup. The same feature is observed in the IR spectra of reverse micelles after deconvoluting the interfacial versus bulk spectral contributions. We performed an orientational analysis of these water molecules utilizing the polarization-dependent SFG spectra, which shows an average tilt angle of the OH stretch of surfactant-bound water molecules of ∼155° with respect to the surface normal.

Dynamics of vortex assisted metal condensation in superfluid helium.

Laser ablation of copper and silver targets immersed in bulk normal and superfluid (4)He was studied through time-resolved shadowgraph photography. In normal fluid, only a sub-millimeter cavitation bubble is created and immediate formation of metal clusters is observed within a few hundred microseconds. The metal clusters remain spatially tightly focused up to 15 ms, and it is proposed that this observation may find applications in particle image velocimetry. In superfluid helium, the cavitation bubble formation process is distinctly different from the normal fluid. Due to the high thermal conductivity and an apparent lag in the breakdown of superfluidity, about 20% of the laser pulse energy was transferred directly into the liquid and a large gas bubble, up to several millimeters depending on laser pulse energy, is created. The internal temperature of the gas bubble is estimated to exceed 9 K and the following bubble cool down period therefore includes two separate phase transitions: gas-normal liquid and normal liquid-superfluid. The last stage of the cool down process was assigned to the superfluid lambda transition where a sudden formation of large metal clusters is observed. This is attributed to high vorticity created in the volume where the gas bubble previously resided. As shown by theoretical bosonic density functional theory calculations, quantized vortices can trap atoms and dimers efficiently, exhibiting static binding energies up to 22 K. This, combined with hydrodynamic Bernoulli attraction, yields total binding energies as high as 35 K. For larger clusters, the static binding energy increases as a function of the volume occupied in the liquid to minimize the surface tension energy. For heliophobic species an energy barrier develops as a function of the cluster size, whereas heliophilics show barrierless entry into vortices. The present theoretical and experimental observations are used to rationalize the previously reported metal nanowire assembly in both superfluid bulk liquid helium and helium droplets, both of which share the common element of a rapid passage through the lambda point. The origin of vorticity is tentatively assigned to the Zurek-Kibble mechanism. Implications of the large gas bubble formation by laser ablation to previous experiments aimed at implanting atomic and dimeric species in bulk superfluid helium are also discussed, and it is proposed that the developed visualization method should be used as a diagnostic tool in such experiments to avoid measurements in dense gaseous environments.