Molecular structure, binding, and disorder in TDBC-Ag plexcitonic assemblies

Plexcitonic assemblies are hybrid materials composed of a plasmonic nanoparticle and molecular or semiconducting emitters whose electronic transitions are strongly coupled to the plasmonic mode. This coupling hybridizes the system modes into upper and lower polariton branches. The strength of the interaction depends on the number of emitters and on their orientation and spatial arrangement relative to the metallic surface. These structural factors have profound consequences for the ensuing photoexcited dynamics. Despite the extensive spectroscopic work on plexcitonic systems, direct understanding of the molecular geometry at the metal interface remains limited. In this work, we present a comprehensive structural characterization of one of the most widely studied plexcitons formed by the cyanine dye 5,5',6,6'-tetrachloro-1,1'-diethyl-3,3'-di(4-sulfobutyl)-benzimidazolocarbocyanine (TDBC) and silver nanoprisms using a combination of NMR, THz-Raman spectroscopy, and DFT calculations. By comparing the signals from the monomeric and aggregated forms of TDBC with that of the plexciton, we identify shared spectral fingerprints that reveal how molecular packing is modified when the aggregate adsorbs on the silver surface. We observe Raman modes specific to plexciton systems, and identify NOESY cross-peaks in the aliphatic region, that along with THz-Raman modes in the 10-400 cm$^{-1}$ region are sensitive indicators of aggregation geometry and adsorption. We find that isolated TDBC monomers adopt an asymmetric conformation in which both sulfobutyl chains lie on the same side of the chromophore, while J-aggregates adopt a symmetric up-down alternation of the chains from molecule to molecule. This work establishes the molecular geometry of a prototypical TDBC-silver plexciton, providing a structural benchmark for understanding geometry-dependent photophysics in hybrid exciton-plasmon systems.

Source: arXiv:2601.22022v1 - http://arxiv.org/abs/2601.22022v1 PDF: https://arxiv.org/pdf/2601.22022v1 Original Link: http://arxiv.org/abs/2601.22022v1