112 research outputs found
Low-Temperature Synthesis Routes to Intermetallic Superconductors
Over the past few years, our group has gained expertise at developing low-temperature solution-based synthetic pathways to complex nanoscale solids, with particular emphasis on nanocrystalline intermetallic compounds. Our synthetic capabilities are providing tools to reproducibly generate intermetallic nanostructures with simultaneous control over crystal structure, composition, and morphology. This DOE-funded project aims to expand these capabilities to intermetallic superconductors. This could represent an important addition to the tools that are available for the synthesis and processing of intermetallic superconductors, which traditionally utilize high-temperature, high-pressure, thin film, or gas-phase vacuum deposition methods. Our current knowledge of intermetallic superconductors suggests that significant enhancements could result from the inherent benefits of low-temperature solution synthesis, e.g. metastable phase formation, control over nanoscale morphology to facilitate size-dependent property studies, robust and inexpensive processability, low-temperature annealing and consolidation, and impurity incorporation (for doping, stoichiometry control, flux pinning, and improving the critical fields). Our focus is on understanding the superconducting properties as a function of synthetic route, crystal structure, crystallite size, and morphology, and developing the synthetic tools necessary to accomplish this. This research program can currently be divided into two classes of superconducting materials: intermetallics (transition metal/post transition metal) and metal carbides/borides. Both involve the development and exploitation of low-temperature synthesis routes followed by detailed characterization of structures and properties, with the goal of understanding how the synthetic pathways influence key superconducting properties of selected target materials. Because of the low-temperature methods used to synthesize them and the nanocrystalline morphologies of many of the products, the superconductors and their nanocrystalline precursors are potentially amenable to inexpensive and large-scale solution-based processing into wires, coatings, films, and templated or patterned structures with nanoscale and microscale features. Also, because of the new synthetic variables that play a key role in the low-temperature formation of intermetallics, the possibility exists to discover new superconductors
Nanostructured Nickel Phosphide as an Electrocatalyst for the Hydrogen Evolution Reaction
Nanoparticles of nickel phosphide (Ni_2P) have been investigated for electrocatalytic activity and stability for the hydrogen evolution reaction (HER) in acidic solutions, under which proton exchange membrane-based electrolysis is operational. The catalytically active Ni_2P nanoparticles were hollow and faceted to expose a high density of the Ni_2P(001) surface, which has previously been predicted based on theory to be an active HER catalyst. The Ni2P nanoparticles had among the highest HER activity of any non-noble metal electrocatalyst reported to date, producing H_2(g) with nearly quantitative faradaic yield, while also affording stability in aqueous acidic media
Electrocatalytic hydrogen evolution using amorphous tungsten phosphide nanoparticles
Amorphous tungsten phosphide (WP), which has been synthesized as colloidal nanoparticles with an average diameter of 3 nm, has been identified as a new electrocatalyst for the hydrogen-evolution reaction (HER) in acidic aqueous solutions. WP/Ti electrodes produced current densities of â10 mA cm^(â2) and â20 mA cm^(â2) at overpotentials of only â120 mV and â140 mV, respectively, in 0.50 M H_2SO_4(aq)
Ternary oxides of - and -block metals for photocatalytic solar-to-hydrogen conversion
Oxides containing metals or metalloids from the {\it p}-block of the periodic
table ({\it e.g.}, In, Sn, Sb, Pb, Bi) are of technological interest as
transparent conductors and light absorbers for solar energy conversion due to
the tunability of their electronic conductivity and optical absorption.
Comparatively, these oxides have found limited applications in hydrogen
photoelectrolysis primarily due to their high electronegativity, which impedes
electron transfer for reducing protons into hydrogen. We have shown recently
that inserting {\it s}-block cations into {\it p}-block metal oxides is
effective at lowering electronegativities while affording further control of
band gaps. Here, we explain the origins of this dual tunability by
demonstrating the mediator role of {\it s}-block cations in modulating orbital
hybridization while not contributing to frontier electronic states. From this
result, we carry out a comprehensive computational study of 109 ternary oxides
of {\it s}- and {\it p}-block metal elements as candidate photocatalysts for
solar hydrogen generation. We downselect the most desirable materials using
band gaps and band edges obtained from Hubbard-corrected density-functional
theory with Hubbard parameters computed entirely from first principles,
evaluate the stability of these oxides in aqueous conditions, and characterize
experimentally four of the remaining materials, synthesized with high phase
uniformity, to validate and further develop the computational models. We thus
propose nine oxide semiconductors, including CsInO, SrInO,
and KSbO which, to the extent of our literature review, have not been
previously considered as water-splitting photocatalysts.Comment: 14 pages, 5 figures, 1 supplemental materia
Amorphous Molybdenum Phosphide Nanoparticles for Electrocatalytic Hydrogen Evolution
Amorphous molybdenum phosphide (MoP) nanoparticles have been synthesized and characterized as electrocatalysts for the hydrogen-evolution reaction (HER) in 0.50 M H_2SO_4 (pH 0.3). Amorphous MoP nanoparticles (having diameters of 4.2 ± 0.5 nm) formed upon heating Mo(CO)6 and trioctylphosphine in squalane at 320 °C, and the nanoparticles remained amorphous after heating at 450 °C in H_2(5%)/Ar(95%) to remove the surface ligands. At mass loadings of 1 mg cm^â2, MoP/Ti electrodes exhibited overpotentials of â90 and â105 mV (â110 and â140 mV without iR correction) at current densities of â10 and â20 mA cm^â2, respectively. These HER overpotentials remained nearly constant over 500 cyclic voltammetric sweeps and 18 h of galvanostatic testing, indicating stability in acidic media under operating conditions. Amorphous MoP nanoparticles are therefore among the most active known molybdenum-based HER systems and are part of a growing family of active, acid-stable, non-noble-metal HER catalysts
Comparison of the Performance of CoP-Coated and Pt-Coated Radial Junction n^+p-Silicon Microwire-Array Photocathodes for the Sunlight-Driven Reduction of Water to H_2(g)
The electrocatalytic performance for hydrogen evolution has been evaluated for radial-junction n^+p-Si microwire (MW) arrays with Pt or cobalt phosphide, CoP, nanoparticulate catalysts in contact with 0.50 M H_2SO_4(aq). The CoP-coated (2.0 mg cm^(â2)) n^+p-Si MW photocathodes were stable for over 12 h of continuous operation and produced an open-circuit photovoltage (V_(oc)) of 0.48 V, a light-limited photocurrent density (J_(ph)) of 17 mA cm^(â2), a fill factor (ff) of 0.24, and an ideal regenerative cell efficiency (η_(IRC)) of 1.9% under simulated 1 Sun illumination. Pt-coated (0.5 mg cm^(â2)) n^+p-Si MW-array photocathodes produced V_(oc) = 0.44 V, J_(ph) = 14 mA cm^(â2), ff = 0.46, and η = 2.9% under identical conditions. Thus, the MW geometry allows the fabrication of photocathodes entirely comprised of earth-abundant materials that exhibit performance comparable to that of devices that contain Pt
Diverse Applications of Nanomedicine
The design and use of materials in the nanoscale size range for addressing medical and health-related issues continues to receive increasing interest. Research in nanomedicine spans a multitude of areas, including drug delivery, vaccine development, antibacterial, diagnosis and imaging tools, wearable devices, implants, high-throughput screening platforms, etc. using biological, nonbiological, biomimetic, or hybrid materials. Many of these developments are starting to be translated into viable clinical products. Here, we provide an overview of recent developments in nanomedicine and highlight the current challenges and upcoming opportunities for the field and translation to the clinic. \ua9 2017 American Chemical Society
- âŠ