Abstract
Solar-driven plasmonic photocatalysis has emerged as a powerful tool to enhance chemical reactivity, improving the efficiency and selectivity in a large number of transformations. Plasmonic nanoparticles are often implemented in photocatalysis as colloidal dispersions but they face issues related to the reduced photoactivation of the metallic surface in concentrated solutions and poor long-term colloidal stability. To overcome these limitations, we introduce 3D plasmonic supercrystals created through the depletion- and evaporation-induced self-assembly of metal nanoparticles as novel heterogeneous plasmonic photocatalysts. They present large electromagnetic field enhancements associated to the formation of regular arrays of plasmonic hot spots, leading to improved chemical reactivities through the generation of hot charge carriers. To demonstrate this, we chose two challenging organic transformations, an oxidative polymerization and different C‒C cross-coupling reactions, that can be activated by modifying the chemical composition of the assemblies. Interestingly, the anisotropic shapes of the building blocks lead to the formation of 3D supercrystals exposing different crystalline facets. Importantly, by performing operando Surface-Enhanced Raman Spectroscopy at the single supercrystal level, we unveil the face-dependent reactivity of each individual plasmonic superstructure. Our combined experimental and theoretical approach provides with key insights into structure-function correlations and offers guidelines for the rational design of versatile supercrystal photocatalysts.