Structural Diversity in Dimension-Controlled Assemblies of Tetrahedral Gold Nanocrystals.

Polyhedron packings have fascinated humans for centuries and continue to inspire scientists of modern disciplines. Despite extensive computer simulations and a handful of experimental investigations, understanding of the phase behaviors of synthetic tetrahedra has remained fragmentary largely due to the lack of tetrahedral building blocks with tunable size and versatile surface chemistry. Here, we report the remarkable richness of and complexity in dimension-controlled assemblies of gold nanotetrahedra. By tailoring nanocrystal interactions from long-range repulsive to hard-particle-like or to systems with short-ranged directional attractions through control of surface ligands and assembly conditions, nearly a dozen of two-dimensional and three-dimensional superstructures including the cubic diamond and hexagonal diamond polymorphs are selectively assembled. We further demonstrate multiply twinned icosahedral supracrystals by drying aqueous gold nanotetrahedra on a hydrophobic substrate. This study expands the toolbox of the superstructure by design using tetrahedral building blocks and could spur future computational and experimental work on self-assembly and phase behavior of anisotropic colloidal particles with tunable interactions.

Multistep Crystallization of Dynamic Nanoparticle Superlattices in Nonaqueous Solutions.

Crystallization is a universal phenomenon underpinning many industrial and natural processes and is fundamental to chemistry and materials science. However, microscopic crystallization pathways of nanoparticle superlattices have been seldom studied mainly owing to the difficulty of real-time observation of individual self-assembling nanoparticles in solution. Here, using in situ electron microscopy, we directly image the full self-assembly pathway from dispersed nanoparticles into ordered superlattices in nonaqueous solution. We show that electron-beam irradiation controls nanoparticle mobility, and the solvent composition largely dictates interparticle interactions and assembly behaviors. We uncover a multistep crystallization pathway consisting of four distinct stages through multi-order-parameter analysis and visualize the formation, migration, and annihilation of multiple types of defects in nanoparticle superlattices. These findings open the door for achieving independent control over imaging conditions and nanoparticle assembly conditions and will enable further study of the microscopic kinetics of assembly and phase transition in nanocolloidal systems.

Unraveling the Structural Sensitivity of CO2 Electroreduction at Facet-Defined Nanocrystals via Correlative Single-Entity and Macroelectrode Measurements.

The conversion of CO2 into value-added products is a compelling way of storing energy derived from intermittent renewable sources and can bring us closer to a closed-loop anthropogenic carbon cycle. The ability to synthesize nanocrystals of well-defined structure and composition has invigorated catalysis science with the promise of nanocrystals that selectively express the most favorable sites for efficient catalysis. The performance of nanocrystal catalysts for the CO2 reduction reaction (CO2RR) is typically evaluated with nanocrystal ensembles, which returns an averaged system-level response of complex catalyst-modified electrodes with each nanocrystal likely contributing a different (unknown) amount. Measurements at single nanocrystals, taken in the context of statistical analysis of a population, and comparison to macroscale measurements are necessary to untangle the complexity of the ever-present heterogeneity in nanocrystal catalysts, achieve true structure-property correlation, and potentially identify nanocrystals with outlier performance. Here, we employ environment-controlled scanning electrochemical cell microscopy to isolate and investigate the electrocatalytic CO2RR response of individual facet-defined gold nanocrystals. Using correlative microscopy approaches, we conclusively demonstrate that {110}-terminated gold rhombohedra possess superior activity and selectivity for CO2RR compared with {111}-terminated octahedra and high-index {310}-terminated truncated ditetragonal prisms, especially at low overpotentials where electrode kinetics is anticipated to dominate the current response. The methodology framework described here could inform future studies of complex electrocatalytic processes through correlative single-entity and macroscale measurement techniques.

Macromolecular Ligand Engineering for Programmable Nanoprism Assembly.

Ligands play a central role for the energetics and kinetics of nanocrystal assembly. Yet, the precise and simultaneous manipulation of ligands to dictate assembly outcome has proven difficult. Here, we present macromolecular ligand-engineering strategies to control, characterize, and model four molecular parameters of grafted polymer chains: chain length, chain dispersity, grafting density, and chain distribution. Direct ligand-exchange between nanoprisms and polymers functionalizes facets selectively and produces patchy nanocrystals. We develop a generalizable two-step ligand-exchange approach for the independent control of the two emergent brush parameters, brush thickness and brush softness. The resultant polymer-grafted prismatic nanocrystals with programmable ligand brushes self-assemble into thin-film superstructures of different wallpaper symmetries and faceted supracrystals. Our experiments are complemented by coarse-grained computer simulations of nanoprisms with directional, facet-specific interactions. This work paves the way for the precision synthesis of polymer-nanocrystal hybrid materials and enables the further refinement of theoretical models for particle brush materials.

Heterometallic Seed-Mediated Growth of Monodisperse Colloidal Copper Nanorods with Widely Tunable Plasmonic Resonances.

We report a heterometallic seed-mediated synthesis method for monodisperse penta-twinned Cu nanorods using Au nanocrystals as seeds. Elemental analyses indicate that resultant nanorods consist predominantly of copper with a gold content typically below 3 atom %. The nanorod aspect ratio can be readily adjusted from 2.8 to 13.1 by varying the molar ratio between Au seeds and Cu precursor, resulting in narrow longitudinal plasmon resonances tunable from 762 to 2201 nm. Studies of reaction intermediates reveal that symmetry-breaking is promoted by rapid nanoscale diffusion in Au-Cu alloys and the formation of a gold-rich surface. The growth pathway features coevolving shape and composition whereby nanocrystals become progressively enriched with Cu concomitant with nanorod growth. The availability of uniform colloidal Cu nanorods with widely tunable aspect ratios opens new avenues toward the synthesis of derivative one-dimensional metal nanostructures, and applications in surface-enhanced spectroscopy, bioimaging, and electrocatalysis, among others.

Broadband Tunable Mid-infrared Plasmon Resonances in Cadmium Oxide Nanocrystals Induced by Size-Dependent Nonstoichiometry.

A central theme of nanocrystal (NC) research involves synthesis of dimension-controlled NCs and studyof size-dependent scaling laws governing their optical, electrical, magnetic, and thermodynamic properties. Here, we describe the synthesis of monodisperse CdO NCs that exhibit high quality-factor (up to 5.5) mid-infrared (MIR) localized surface plasmon resonances (LSPR) and elucidate the inverse scaling relationship between carrier concentration and NC size. The LSPR wavelength is readily tunable between 2.4 and ∼6.0 µm by controlling the size of CdO NCs. Structural and spectroscopic characterization provide strong evidence that free electrons primarily originate from self-doping due to NC surface-induced nonstoichiometry. The ability to probe and to control NC stoichiometry and intrinsic defects will pave the way toward predictive synthesis of doped NCs with desirable LSPR characteristics.

Manipulating atomic defects in plasmonic vanadium dioxide for superior solar and thermal management.

Vanadium dioxide (VO2) is a unique active plasmonic material due to its intrinsic metal-insulator transition, remaining less explored. Herein, we pioneer a method to tailor the VO2 surface plasmon by manipulating its atomic defects and establish a universal quantitative understanding based on seven representative defective VO2 systems. Record high tunability is achieved for the localized surface plasmon resonance (LSPR) energy (0.66-1.16 eV) and transition temperature range (40-100 °C). The Drude model and density functional theory reveal that the charge of cations plays a dominant role in the numbers of valence electrons to determine the free electron concentration. We further demonstrate their superior performances in extensive unconventional plasmonic applications including energy-saving smart windows, wearable camouflage devices, and encryption inks.

Tuning infrared plasmon resonances in doped metal-oxide nanocrystals through cation-exchange reactions.

Metal-oxide nanocrystals doped with aliovalent atoms can exhibit tunable infrared localized surface plasmon resonances (LSPRs). Yet, the range of dopant types and concentrations remains limited for many metal-oxide hosts, largely because of the difficulty in establishing reaction kinetics that favors dopant incorporation by using the co-thermolysis method. Here we develop cation-exchange reactions to introduce p-type dopants (Cu+, Ag+, etc.) into n-type metal-oxide nanocrystals, producing programmable LSPR redshifts due to dopant compensation. We further demonstrate that enhanced n-type doping can be realized via sequential cation-exchange reactions mediated by the Cu+ ions. Cation-exchange transformations add a new dimension to the design of plasmonic nanocrystals, allowing preformed nanocrystals to be used as templates to create compositionally diverse nanocrystals with well-defined LSPR characteristics. The ability to tailor the doping profile postsynthetically opens the door to a multitude of opportunities to deepen our understanding of the relationship between local structure and LSPR properties.

Thermosensitive polymer controlled morphogenesis and phase discrimination of calcium carbonate.

Homogeneous aragonite flowers with controlled surface structures can be synthesized by using a thermosensitive polymer, i.e. poly (ethylene glycol)-poly(N-isopropyl acrylamide)-poly(acrylamido methyl propane sulfonate) (PEG-PNIPAM-PAMPS), as a crystal growth modifier in the mineralization of calcium carbonate.