Molecular Decoupling and Surface Coverage Synergistically Contribute to the Volcano-Shaped Probability of Single-Molecule-Level Chemical Reactions at the Surface

Deciphering single-molecule-level chemical reactions at surfaces requires elucidating the synergistic effect of molecular decoupling and spatial distribution. However, this can only be achieved using a limited number of experimental techniques. Here, we demonstrate for the first time that nanocavity-enhanced sum-frequency generation vibrational imaging provides a powerful tool for visualizing both molecular decoupling and spatial distribution of ultralow-concentration molecules in plasmonic nanocavities. Using 4-nitrothiophenol as a model system, we observed a pronounced aggregation effect in molecular self-assembly and a volcano-shaped reaction probability curve in interfacial single-molecule-level chemical reactions. This volcano shape arises from the balance between two competing factors: enhanced reactivity due to molecular decoupling and decreased reaction probability due to reduced molecular availability. This study establishes a molecular-level correlation between intermolecular coupling, surface coverage, and reactivity, thereby paving the way for investigating and manipulating interfacial single-molecule-level chemical reactions.