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Noble metal nanoplates are a unique class of two-dimensional (2D) nanomaterials whose planar geometry serves as one of the most important nanoscale building blocks. Referred to by names such as nanoplates, nanodisks, nanoprisms, and nanotriangles, they offer a distinct and compelling set of physicochemical properties renowned for their plasmonic response and catalytic activity. When immobilized on substrates, these same structures are empowered with new capabilities triggered by synergistic interactions with their support and coupling phenomena activated when adjacent nanostructures are held in place with nanometer-scale spacings. In this review, we bring together an impressive literature dedicated to the synthesis, assembly, and application of substrate-immobilized noble metal nanoplates where we highlight the interplay between the nanostructures and their support as a means for deriving a distinct and diverse product. Methods for obtaining substrate-bound nanoplates rely on colloid-to-substrate transfers or syntheses occurring directly on the substrate-surface and span a wide range of techniques including chemisorption, solvent evaporation assembly, air–liquid interfacial assembly, substrate- and seed-mediated syntheses, electrochemical syntheses, vapor-phase depositions, DNA-assisted assembly, and capillary assembly. Collectively, these techniques realize nanoplate formations that are random, close-packed assemblies, periodic arrays, and three-dimensional superlattices. Nanoplate functionality is demonstrated in sensor applications with a broad range of analytes that include explosives, environmentally persistent pollutants, illicit drugs, and microRNA biomarkers for cancer and cardiovascular disease, with proof-of-concept demonstrations as active plasmonics, skin-mountable sensors, point-of-care diagnostics, and electrochemical reactors. Together, this work demonstrates substrate-immobilized nanoplates as a powerful platform for realizing photo- and chemically-active surfaces of technological relevance. 

With arms radiating from a central core, gold nanostars represent a unique and fascinating class of nanomaterials from which extraordinary plasmonic properties are derived. Despite their relevance to sensing applications, methods for fabricating homogeneous populations of nanostars on large-area planar surfaces in truly periodic arrays is lacking. Herein, the fabrication of nanostar arrays is demonstrated through the formation of hexagonal patterns of near-hemispherical gold seeds and their subsequent exposure to a liquid-state chemical environment that is conducive to colloidal nanostar formation. Three different colloidal nanostar protocols were targeted where HEPES, DMF, and ascorbic acid represent a key reagent in their respective redox chemistries. Only the DMF-driven synthesis proved readily adaptable to the substrate-based platform but nanostar-like structures emerged from the other protocols when synthetic controls such as reaction kinetics, the addition of Ag + ions, and pH adjustments were applied. Because the nanostars were derived from near-hemispherical seeds, they acquired a unique geometry that resembles a conventional nanostar that has been truncated near its midsection. Simulations of plasmonic properties of this geometry reveal that such structures can exhibit maximum near-field intensities that are as much as seven-times greater than the standard nanostar geometry, a finding that is corroborated by surface-enhanced Raman scattering (SERS) measurements showing large enhancement factors. The study adds nanostars to the library of nanostructure geometries that are amenable to large-area periodic arrays and provides a potential pathway for the nanofabrication of SERS substrates with even greater enhancements.