Spatial Variations in Hydrogen Bonding Interaction within Polymer Blends Revealed by Infrared Nanoimaging.

Hydrogen bonding plays a crucial role in enhancing the miscibility of polymer blends, allowing for the tailoring of their physicochemical properties to meet diverse application demands. However, nanoscale imaging of its impact on the phase-separation behavior of multicomponent polymeric materials remains largely unexplored. In this work, we introduce scattering-type scanning near-field optical microscopy (s-SNOM) equipped with a broadly tunable quantum cascade laser as a tool for investigating spatial variations in hydrogen-bonding interactions within blends of polyvinyl acetate (PVAc) and polyvinylphenol (PVPh), spin-coated from tetrahydrofuran solution.

Scouting for strong light-matter coupling signatures in Raman spectra.

Strong coupling between vibrational transitions and a vacuum field of a cavity mode leads to the formation of vibrational polaritons. These hybrid light-matter states have been widely explored because of their potential to control chemical reactivity. However, the possibility of altering Raman scattering through the formation of vibrational polaritons has been rarely reported.

Multimode Vibrational Strong Coupling of Methyl Salicylate to a Fabry-Pérot Microcavity.

The strong coupling of an IR-active molecular transition with an optical mode of the cavity results in vibrational polaritons, which opens a new way to control chemical reactivity via confined electromagnetic fields of the cavity. In this study, we design a voltage-tunable open microcavity and we show the formation of multiple vibrational polaritons in methyl salicylate. A Rabi splitting and polariton anticrossing behavior is observed when the cavity mode hybridizes with the C═O stretching vibration of methyl salicylate.