By using octahedral gold nanocrystals with sizes of approximately 50 nm as the structure-directing cores for the overgrowth of Pd shells, Au-Pd core-shell heterostructures with systematic shape evolution can be directly synthesized. Core-shell octahedra, truncated octahedra, cuboctahedra, truncated cubes, and concave cubes were produced by progressively decreasing the amount of the gold nanocrystal solution introduced into the reaction mixture containing cetyltrimethylammonium bromide (CTAB), H(2)PdCl(4), and ascorbic acid. The core-shell structure and composition of these nanocrystals has been confirmed. Only the concave cubes are bounded by a variety of high-index facets. This may be a manifestation of the release of lattice strain with their thick shells at the corners. Formation of the [CTA](2)[PdBr(4)] complex species has been identified spectroscopically. Time-dependent UV-vis absorption spectra showed faster Pd source consumption rates in the growth of truncated cubes and concave cubes, while a much slower reduction rate was observed in the generation of octahedra. The concave cubes and octahedra were used as catalysts for a Suzuki coupling reaction. They can all serve as effective and recyclable catalysts, but the concave cubes gave higher product yields with a shorter reaction time attributed to their high-index surface facets. The concave cubes can also catalyze a wide range of Suzuki coupling reactions using aryl iodides and arylboronic acids with electron-donating and -withdrawing substituents.

AC O 2-mediated hydrogen storage energy cycle is ap romising wayt oi mplement ah ydrogen economy,b ut the exploration of efficient catalysts to achieve this process remains challenging.H erein, sub-nanometer Pd-Mn clusters were encaged within silicalite-1 (S-1) zeolites by al igand-protected method under direct hydrothermal conditions.T he obtained zeolite-encaged metallic nanocatalysts exhibited extraordinary catalytic activity and durability in both CO 2 hydrogenation into formate and formic acid (FA) dehydrogenation backt oC O 2 and hydrogen. Thanks to the formation of ultrasmall metal clusters and the synergic effect of bimetallic components,t he PdMn 0.6 @S-1 catalyst afforded af ormate generation rate of 2151 mol formate mol Pd À1 h À1 at 353 K, and an initial turnover frequency of 6860 mol H 2 mol Pd À1 h À1 for CO-free FA decomposition at 333 Kw ithout any additive.B oth values represent the top levels among state-of-the-art heterogeneous catalysts under similar conditions.This work demonstrates that zeoliteencaged metallic catalysts hold great promise to realizeC O 2mediated hydrogen energy cycles in the future that feature fast charge and release kinetics.

This study reports a systematic approach to synthesize ultralong gold nanorods and nanowires using a seed-mediated growth approach. In the first series, the effect of growth solution pH on the lengths of nanorods prepared was investigated. Interestingly, although shorter rods (230-310 nm) were produced in a basic solution environment than in an acidic condition (330-410 nm), the nanorod yield is greatly improved with relatively few nanoplate byproducts formed. Nanorod growth proceeds quickly in a basic solution as evidenced by the fast solution color changes. By adjusting several experimental parameters with the aim to elongate the nanorod length in a tunable fashion, gold nanorods and nanowires with average lengths from 580 to 2850 nm can be synthesized by progressively increasing the HNO3 concentration in the final growth solution. Nanowire growth in a highly acidic solution is slower, and a substantially longer time is needed to reach long lengths. Further extension of the nanowire length can be achieved simply by reducing the volume of second growth solution transferred to the final growth solution. Nanorods and nanowires with lengths spanning from 700 nm to 4.5 μm were prepared in this series of experimental conditions. The longest nanowires can reach a length of up to 6 μm. The nanowires still maintain thin average diameters of 33-53 nm. The ability to make gold nanorods and nanowires over this exceptionally wide and useful length range is exciting because applications and demonstrations using ultralong gold nanorods and nanowires of most suitable lengths are now possible.

Gold supercrystals with polyhedral morphologies can be prepared from the ordered packing of octahedral and rhombic dodecahedral nanocrystals in the presence of a sufficient amount of surfactant by slow water droplet evaporation. The whole supercrystal formation process has been video-recorded using a specially designed chamber to enclose a substrate containing the nanocrystal droplet in a moist environment. Supercrystal growth from the assembly of octahedra is completed within a shorter time. The presence of cetyltrimethylammonium chloride (CTAC) within the supercrystals has been confirmed by small-angle X-ray diffraction analysis. Transmission electron microscopy examination reveals the tendency of two gold octahedra with face contact to fuse, a process frequently observed in the formation of octahedron-assembled supercrystals. Remarkably, we have developed a diffusional surfactant transport approach to make freestanding supercrystals in bulk aqueous solution by adding a concentrated CTAC solution to a concentrated particle solution with a lower CTAC concentration in an Eppendorf tube. Gradual diffusion of CTAC to the lower nanocrystal solution promotes the growth of polyhedral supercrystals. A solution with a sufficiently high surfactant concentration has been shown to be necessary for particle aggregation and supercrystal formation. This method allows the deposition of dense but evenly distributed supercrystals on a substrate. Supercrystals were also used to make a modified electrode for electro-oxidation of glucose. This simple and organic solvent-free approach to making a large quantity of supercrystals allows an ample supply of supercrystals for studies of densely assembled nanocrystal systems and for biomedical applications.

Au-Pd core-shell nanocrystals with cubic, truncated cubic, cuboctahedral, truncated octahedral, and octahedral structures have been employed to form micrometer-sized polyhedral supercrystals by both the droplet evaporation method and novel surfactant diffusion methods. Observation of cross-sectional samples indicates shape preservation of interior nanocrystals within a supercrystal. Low-angle X-ray diffraction techniques and electron microscopy have been used to confirm the presence of surfactant between contacting nanocrystals. By diluting the nanocrystal concentration or increasing the solution temperature, supercrystal size can be tuned gradually to well below 1 μm using the surfactant diffusion method. Rectangular supercrystal microbars were obtained by increasing the amounts of cubic nanocrystals and surfactant used. Au-Ag core-shell cubes and PbS cubes with sizes of 30-40 nm have also been fabricated into supercrystals, showing the generality of the surfactant diffusion approach to form supercrystals with diverse composition. Electrical conductivity measurements on single Au-Pd supercrystals reveal loss of metallic conductivity due to the presence of insulating surfactant. Cubic Au-Pd supercrystals show infrared absorption at 3.2 μm due to extensive plasmon coupling. Mie-type resonances centered at 9.8 μm for the Au-Pd supercrystals disappear once the Pd shells are converted into PdH after hydrogen absorption.