In this work, a pioneering study on the electrical properties of composite carbon nanofibres (CNFs) using current-sensitive atomic force microscopy (CS-AFM) has been demonstrated.

Vibrational sum frequency spectra (vSFS) of 4-nitrothiophenol (4-NTP) have been utilized to study plasmonic effects arising from its interaction with gold nanoparticles (Au NPs). To this end three systems have been studied: 4-NTP adsorbed on deposited Au nanoparticles, a self-assembled monolayer of 4-NTP on flat Au with dispersed Au NPs atop and, as reference, a self-assembled monolayer of 4-NTP. For 4-NTP on 50 and 80 nm Au NPs an enhancement of the SF intensity due to plasmonic effects by less than 1 order of magnitude is inferred in comparison to the monolayer system after taking the particle density into account. The addition of Au NPs to the monolayer system on flat Au also selectively enhances the response to an in-plane field component of the 532 nm upconversion light.

Surface-sensitive vibrational sum frequency spectroscopy (vSFS) has been utilized to study the adsorption chemistry of small alcohols, namely, methanol, ethanol, 1propanol, and 2-propanol on TiO 2 thin films under near-ambient conditions. The vSF spectra in the C−H region reveal that methanol and ethanol adsorb both molecularly and dissociatively, while 1-propanol and 2-propanol are solely detected in the molecular form. The different adsorption behavior suggests that the extent of dissociation decreases from methanol to propanol. Moreover, polarization analysis of the spectra reveals that the methyl groups are preferentially oriented with their symmetry axis pointing in a direction close to the surface normal for methanol, ethanol, and 1-propanol. However, for 2-propanol, the methyl groups exhibit a larger tilt angle.

A detailed study of the adsorption structure of self-assembled monolayers of 4-nitrothiophenol on the Au(111) surface was performed from a theoretical perspective via first-principles density functional theory calculations and experimentally by Raman and vibrational sum frequency spectroscopy (vSFS) with an emphasis on the molecular orientation. Simulations—including an explicit van der Waals (vdW) description—for different adsorbate structures, namely, for (3×3), (2 × 2), and (3 × 3) surface unit cells, reveal a significant tilting of the molecules toward the surface with decreasing coverage from 75° down to 32° tilt angle. vSFS suggests a tilt angle of 50°, which agrees well with the one calculated for a structure with a coverage of 0.25. Furthermore, calculated vibrational eigenvectors and spectra allowed us to identify characteristic in-plane (NO2 scissoring) and out-of-plane (C–H wagging) modes and to predict their strength in the spectrum in dependence of the adsorption geometry. We additionally performed calculations for biphenylthiol and terphenylthiol to assess the impact of multiple aromatic rings and found that vdW interactions are significantly increasing with this number, as evidenced by the absorption energy and the molecule adopting a more upright-standing geometry.

The interaction of 2-propanol with Co3O4(001) was studied by vibrational sum frequency spectroscopy and ab initio molecular dynamics simulations of 2-propanol dissolved in a water film to gain an insight, at the molecular level, into the pathways of catalytic oxidation. The experimental study has been performed under near ambient conditions, where the presence of water vapor is unavoidable, resulting in a water film on the sample and, thereby, allowing us to mimic the solution–water interface. Both experiment and theory conclude that 2-propanol adsorbs molecularly. The lack of dissociation is attributed to the adsorption geometry of 2-propanol in which the O–H bond does not point toward the surface. Furthermore, the copresent water not only competitively adsorbs on the surface but also inhibits 2-propanol deprotonation. The calculations reveal that the presence of water deactivates the lattice oxygen, thereby reducing the surface activity. This finding sheds light on the multifaceted role of water at the interface for the electrochemical oxidation of 2-propanol in aqueous solution as recently reported [Falk et al., ChemCatChem 13, 2942–2951 (2021)]. At higher temperatures, 2-propanol remains molecularly adsorbed on Co3O4(001) until it desorbs with increasing surface temperature.