Monolithic Nanoporous Gold Foams with Catalytic Activity for Chemical Vapor Deposition Growth of Carbon Nanostructures.

While bulk gold is generally considered to be a catalytically inactive material, nanostructured forms of gold can in fact be highly catalytically active. However, few methods exist for preparing high-purity macroscopic forms of catalytically active gold. In this work, we describe the synthesis of catalytically active macroscopic nanoporous gold foams via combustion synthesis of gold bis(tetrazolato)amine complexes. The resulting metallically pure porous gold nanoarchitectures exhibit bulk densities of <0.1 g/cm3 and Brunauer-Emmett-Teller (BET) surface areas as high as 10.9 m2/g, making them among the lowest-density and highest-surface-area monolithic forms of gold produced to date. Thanks to the presence of a highly nanostructured gold surface, such gold nanofoams have also been found to be highly catalytically active toward thermal chemical vapor deposition (CVD) growth of carbon nanotubes, providing a novel method for direct synthesis of carbon nanostructures on macroscopic gold substrates. In contrast, analogous copper nanofoams were found to be catalytically inactive toward the growth of graphitic nanostructures under the same synthesis conditions, highlighting the unusually high catalytic propensity of this form factor of gold. The combustion synthesis process described herein represents a never-wet approach for directly synthesizing macroscopic catalytically active gold. Unlike sol-gel and dealloying approaches, combustion synthesis eliminates the time-consuming diffusion-mediated steps associated with previous methods and offers multiple degrees of freedom for tuning morphology, electrical conductivity, and mechanical properties.

The SuperCam Instrument Suite on the NASA Mars 2020 Rover: Body Unit and Combined System Tests.

The SuperCam instrument suite provides the Mars 2020 rover, Perseverance, with a number of versatile remote-sensing techniques that can be used at long distance as well as within the robotic-arm workspace. These include laser-induced breakdown spectroscopy (LIBS), remote time-resolved Raman and luminescence spectroscopies, and visible and infrared (VISIR; separately referred to as VIS and IR) reflectance spectroscopy. A remote micro-imager (RMI) provides high-resolution color context imaging, and a microphone can be used as a stand-alone tool for environmental studies or to determine physical properties of rocks and soils from shock waves of laser-produced plasmas. SuperCam is built in three parts: The mast unit (MU), consisting of the laser, telescope, RMI, IR spectrometer, and associated electronics, is described in a companion paper. The on-board calibration targets are described in another companion paper. Here we describe SuperCam's body unit (BU) and testing of the integrated instrument. The BU, mounted inside the rover body, receives light from the MU via a 5.8 m optical fiber. The light is split into three wavelength bands by a demultiplexer, and is routed via fiber bundles to three optical spectrometers, two of which (UV and violet; 245-340 and 385-465 nm) are crossed Czerny-Turner reflection spectrometers, nearly identical to their counterparts on ChemCam. The third is a high-efficiency transmission spectrometer containing an optical intensifier capable of gating exposures to 100 ns or longer, with variable delay times relative to the laser pulse. This spectrometer covers 535-853 nm ( 105 - 7070 cm - 1 Raman shift relative to the 532 nm green laser beam) with 12 cm - 1 full-width at half-maximum peak resolution in the Raman fingerprint region. The BU electronics boards interface with the rover and control the instrument, returning data to the rover. Thermal systems maintain a warm temperature during cruise to Mars to avoid contamination on the optics, and cool the detectors during operations on Mars. Results obtained with the integrated instrument demonstrate its capabilities for LIBS, for which a library of 332 standards was developed. Examples of Raman and VISIR spectroscopy are shown, demonstrating clear mineral identification with both techniques. Luminescence spectra demonstrate the utility of having both spectral and temporal dimensions. Finally, RMI and microphone tests on the rover demonstrate the capabilities of these subsystems as well.

Evidence of a kinetic isotope effect in nanoaluminum and water combustion.

The normally innocuous combination of aluminum and water becomes violently reactive on the nanoscale. Research in the field of the combustion of nanoparticulate aluminum has important implications in the design of molecular aluminum clusters, hydrogen storage systems, as well as energetic formulations which could use extraterrestrial water for space propulsion. However, the mechanism that controls the reaction speed is poorly understood. While current models for micron-sized aluminum water combustion reactions place heavy emphasis on diffusional limitations, as reaction scales become commensurate with diffusion lengths (approaching the nanoscale) reaction rates have long been suspected to depend on chemical kinetics, but have never been definitely measured. The combustion analysis of nanoparticulate aluminum with H2O or D2O is presented. Different reaction rates resulting from the kinetic isotope effect are observed. The current study presents the first-ever observed kinetic isotope effect in a metal combustion reaction and verifies that chemical reaction kinetics play a major role in determining the global burning rate.

Controlled assembly of zero-, one-, two-, and three-dimensional metal chalcogenide structures.

A room-temperature solution route to the controlled synthesis of 0-, 1-, 2-, and 3-D assemblies of molecularly linked metal chalcogenide clusters using essentially identical building blocks is reported. The solvating, ligating, and reducing abilities of hydrazine at room temperature have been exploited to simultaneously dissolve metal chalcogenides and organize the resulting building blocks into frameworks of increasing dimensionalities. Control of the product dimensionality was achieved by varying the reactant ratios and the amount of hydrazine solvent employed in the reaction. The products have been characterized by single-crystal X-ray diffraction, Raman spectroscopy, and magnetic susceptibility.