Hydration and Orientation of Carbonyl Groups in Oppositely Charged Lipid Monolayers on Water.

The carbonyl groups of glycerolipid monolayers on water play an important role in the formation of the interfacial hydrogen bond network, which in turn influences the interactions of lipids with, for example, metabolites. As the frequency of the carbonyl absorption band strongly depends on the hydration state of the lipid headgroups, the carbonyl band is a sensitive reporter of changes in the headgroup environment. Here, we use phase-resolved sum frequency generation spectroscopy to obtain information about the orientation and hydration of the carbonyl groups in lipid monolayers. We find that there are two distinct carbonyl moieties in the lipid monolayers, oppositely oriented relative to the surface plane, that experience substantially different hydrogen-bonding environments.

Surface-Specific Spectroscopy of Water at a Potentiostatically Controlled Supported Graphene Monolayer.

Knowledge of the structure of interfacial water molecules at electrified solid materials is the first step toward a better understanding of important processes at such surfaces, in, e.g., electrochemistry, atmospheric chemistry, and membrane biophysics. As graphene is an interesting material with multiple potential applications such as in transistors or sensors, we specifically investigate the graphene-water interface. We use sum-frequency generation spectroscopy to investigate the pH- and potential-dependence of the interfacial water structure in contact with a chemical vapor deposited (CVD) grown graphene surface. Our results show that the SFG signal from the interfacial water molecules at the graphene layer is dominated by the underlying substrate and that there are water molecules between the graphene and the (hydrophilic) supporting substrate.

Surface Potential of a Planar Charged Lipid-Water Interface. What Do Vibrating Plate Methods, Second Harmonic and Sum Frequency Measure?

The interfacial electrical potential is an important parameter influencing, for instance, electrochemical reactions and biomolecular interactions at membranes. A deeper understanding of different methods that measure quantities related to the surface potential is thus of great scientific and technological relevance. We use lipid monolayers with varying charge density and thoroughly compare the results of surface potential measurements performed with the vibrating plate capacitor method and second harmonic generation spectroscopy. The two techniques provide very different results as a function of surface charge. Using the molecular information on lipid alkyl chain, lipid headgroup, and interfacial water provided by sum frequency generation spectroscopy, we disentangle the different contributions to the surface potential measured by the different techniques. Our results show that the two distinct approaches are dominated by different molecular moieties and effects. While the shape of the SPOT method response as a function of charge density is dominated by the lipid carbonyl groups, the SHG results contain contributions from the interfacial water molecules, the lipids and hyper-Rayleigh scattering.