Ningmu Zou

This review discusses the latest advances in using single-molecule microscopy of fluorogenic reactions to examine and understand the spatiotemporal catalytic behaviors of single metal nanoparticles of various shapes including pseudospheres, nanorods, and nanoplates. Real-time single-turnover kinetics reveal size-, catalysis-, and metal-dependent temporal activity fluctuations of single pseudospherical nanoparticles (<20 nm in diameter). These temporal catalytic dynamics can be related to nanoparticles' dynamic surface restructuring whose timescales and energetics can be quantified. Single-molecule super-resolution catalysis imaging further enables the direct quantification of catalytic activities at different surface sites (i.e., ends vs. sides, or corner, edge vs. facet regions) on single pseudo 1-D and 2-D nanocrystals, and uncovers linear and radial activity gradients within the same surface facets. These spatial activity patterns within single nanocrystals can be attributed to the inhomogeneous distributions of low-coordination surface sites, including corner, edge, and defect sites, among which the distribution of defect sites is correlated with the nanocrystals' morphology and growth mechanisms. A brief discussion is given on the extension of the single-molecule imaging approach to catalysis that does not involve fluorescent molecules.

Surface-plasmon (SP) enhanced catalysis on plasmonic nanostructures brings opportunities to increase catalytic efficiency and alter catalytic selectivity. Understanding the underlying mechanism requires quantitative measurements of catalytic enhancement on these nanostructures, whose intrinsic structural heterogeneity presents experimental challenges. Using correlated super-resolution fluorescence microscopy and electron microscopy, here we report a quantitative visualization of SP-enhanced catalytic activity at the nanoscale within single plasmonic nanostructures. We focus on two Au- and Ag-based linked nanostructures that present plasmonic hotspots at nanoscale gaps. Spatially localized higher reaction rates at these gaps vs nongap regions report the SP-induced catalytic enhancements, which show direct correlations with the nanostructure geometries and local electric field enhancements. Furthermore, the catalytic enhancement scales quadratically with the local actual light intensity, attributable to hot electron involvement in the catalytic enhancement mechanism. These discoveries highlight the effectiveness of correlated super-resolution and electron microscopy in interrogating nanoscale catalytic properties.