Yimei Zhu

Pd-Pt Bimetallic Nanodendrites with High Activity for Oxygen Reduction

Extending Platinum Catalysts Platinum performs extremely well as a catalyst for the oxygen-reduction reaction that runs under highly acidic conditions in proton-exchange membrane fuel cells, but is expensive. One strategy for reducing costs is to increase the surface area of the platinum. Lim et al. (p. 1302, published online 14 May) describe a simple chemical route, in which Pt ions in solution are reduced onto Pd seed crystals, which creates faceted Pt nanocrystals with a high area owing to their dendritic architecture. On a Pt mass basis, these catalysts are several times more active than conventional Pt catalysts. The catalytic activity of platinum is enhanced through a growth process that creates nanocrystals with high surface area. Controlling the morphology of Pt nanostructures can provide a great opportunity to improve their catalytic properties and increase their activity on a mass basis. We synthesized Pd-Pt bimetallic nanodendrites consisting of a dense array of Pt branches on a Pd core by reducing K2PtCl4 with L-ascorbic acid in the presence of uniform Pd nanocrystal seeds in an aqueous solution. The Pt branches supported on faceted Pd nanocrystals exhibited relatively large surface areas and particularly active facets toward the oxygen reduction reaction (ORR), the rate-determining step in a proton-exchange membrane fuel cell. The Pd-Pt nanodendrites were two and a half times more active on the basis of equivalent Pt mass for the ORR than the state-of-the-art Pt/C catalyst and five times more active than the first-generation supportless Pt-black catalyst.

Hydrogen‐Evolution Catalysts Based on Non‐Noble Metal Nickel–Molybdenum Nitride Nanosheets

Hydrogen production through splitting of water has attracted great scientific interest because of its relevance to renewable energy storage and its potential for providing energy without the emission of carbon dioxide. Electrocatalytic systems for H2 generation typically incorporate noble metals such as Pt in the catalysts because of their low overpotential and fast kinetics for driving the hydrogen evolution reaction (HER). However, the high costs and limited world-wide supply of these noble metals make their application in viable commercial processes unattractive. Several non-noble metal materials, such as transition-metal chalcogenides, carbides, and complexes as well as metal alloys have been widely investigated recently, and characterized as catalysts and supports for application in the evolution of hydrogen. Nitrides of early transition-metals have been shown to have excellent catalytic activities in a variety of reactions. One of the primary interests in the applications of nitrides in these reactions was to use them in conjunction with low-cost alternative metals to replace group VIII noble metals. For example, the function of molybdenum nitride as a catalyst for hydrocarbon hydrogenolysis resembles that of platinum. The catalytic and electronic properties of transition-metal nitrides are governed by their bulk and surface structure and stoichiometry. While there is some information concerning the effect of the bulk composition on the catalytic properties of this material, there is currently little known about the effects of the surface nanostructure. Nickel and nickel–molybdenum are known electrocatalysts for hydrogen production in alkaline electrolytes, and in the bulk form they exhibited exchange current densities between 10 6 and 10 4 Acm , compared to 10 3 Acm 2 for Pt. Jaksic et al. postulated a hypo-hyper-d-electronic interactive effect between Ni and Mo that yields the synergism for the HER. Owing to their poor corrosion stability, few studies in acidic media have been reported.With the objective of exploiting the decrease in the overpotential by carrying out the HER in acidic media, we have developed a low-cost, stable, and active molybdenum-nitride-based electrocatalyst for the HER. Guided by the “volcano plot” in which the activity for the evolution of hydrogen as a function of the M H bond strength exhibits an ascending branch followed by a descending branch, peaking at Pt, we designed a material on the molecular scale combining nickel, which binds H weakly, with molybdenum, which binds H strongly. Here we report the first synthesis of NiMo nitride nanosheets on a carbon support (NiMoNx/C), and demonstrate the high HER electrocatalytic activity of the resulting NiMoNx/C catalyst with low overpotential and small Tafel slope. The NiMoNx/C catalyst was synthesized by reduction of a carbon-supported ammonium molybdate [(NH4)6Mo7O24·4H2O] and nickel nitrate (Ni(NO3)2·4H2O) mixture in a tubular oven in H2 at 400 8C, and subsequent reaction with NH3 at 700 8C. During this process, the (NH4)6Mo7O24 and Ni(NO3)2 precursors were reduced to NiMo metal particles by H2, and then they were mildly transformed to NiMoNx nanosheets by reaction with ammonia. The atomic ratio of Ni/Mo was 1/4.7 determined by energy dispersive X-ray spectroscopy (EDX) on the NiMoNx/ C sample. The transmission electron microscopy (TEM) images, as shown in Figure 1a, display NiMo particles that are mainly spherical. The high-resolution TEM image, as shown in the inset of Figure 1a, corroborated the presence of an amorphous 3 to 5 nm Ni/Mo oxide layer (see Figure S4 in the Supporting Information for resolved image), whereas NiMoNx is characterized by thin, flat, and flaky stacks composed of nanosheets with high radial-axial ratios (Figure 1b and Figure S5 in the Supporting Information for a magnified image). Figure 1c shows that some of the nanosheets lay flat on the graphite carbon (as indicated by the black arrows), and some have folded edges that show different layers of NiMoNx sheets (white arrows). The thickness of the sheets ranged from 4 to 15 nm. The average stacking number of sheets measured from Figure 1b is about [*] Dr. W.-F. Chen, Dr. K. Sasaki, Dr. J. T. Muckerman, Dr. R. R. Adzic Chemistry Department, Brookhaven National Laboratory Upton, NY 11973 (USA) E-mail: ksasaki@bnl.gov

Highly active and durable nanostructured molybdenum carbide electrocatalysts for hydrogen production

In an attempt to tailor low-cost, precious-metal-free electrocatalysts for water electrolysis in acid, molybdenum carbide (β-Mo2C) nanoparticles are prepared by in situ carburization of ammonium molybdate on carbon nanotubes and XC-72R carbon black without using any gaseous carbon source. The formation of Mo2C is investigated by thermogravimetry and in situ X-ray diffraction. X-ray absorption analysis reveals that Mo2C nanoparticles are inlaid or anchored into the carbon supports, and the electronic modification makes the surface exhibit a relatively moderate Mo–H bond strength. It is found that carbon nanotube-supported Mo2C showed superior electrocatalytic activity and stability in the hydrogen evolution reaction (HER) compared to the bulk Mo2C. An overpotential of 63 mV for driving 1 mA cm−2 of current density was measured for the nanotube-supported Mo2C catalysts; this exceeds the activity of analogous Mo2C catalysts. The enhanced electrochemical activity is facilitated by unique effects of the anchored structure coupled with the electronic modification.

Graphene modified LiFePO4 cathode materials for high power lithium ion batteries

Graphene-modified LiFePO4 composite has been developed as a Li-ion battery cathode material with excellent high-rate capability and cycling stability. The composite was prepared with LiFePO4 nanoparticles and graphene oxide nanosheets by spray-drying and annealing processes. The LiFePO4 primary nanoparticles embedded in micro-sized spherical secondary particles were wrapped homogeneously and loosely with a graphene 3D network. Such a special nanostructure facilitated electron migration throughout the secondary particles, while the presence of abundant voids between the LiFePO4 nanoparticles and graphene sheets was beneficial for Li+ diffusion. The composite cathode material could deliver a capacity of 70 mAh g−1 at 60C discharge rate and showed a capacity decay rate of <15% when cycled under 10C charging and 20C discharging for 1000 times.

Structure of chemically derived mono- and few-atomic-layer boron nitride sheets

We prepared mono- and few-layer hexagonal boron nitride sheets by a chemical-solution-derived method starting from single-crystalline hexagonal boron nitride. Using high-resolution transmission electron microscopy and electron-energy-loss spectrometry, we characterized the microstructure, composition, and near-edge fine structure of the boron nitride sheets. We conclude that the fringe contrast in the edge and the moire patterns are feasible criteria for determining the number of layers and their stacking orientation in the sheets. These criteria are also useful for other mono- and few-layer materials, such as graphene sheets.

Controlling the Shapes of Silver Nanocrystals with Different Capping Agents

This paper provides direct evidence to support the role of a capping agent in controlling the evolution of Ag seeds into nanocrystals with different shapes. Starting with single-crystal seeds (spherical or cubic in shape), we could selectively obtain Ag octahedrons enclosed by {111} facets and nanocubes/nanobars enclosed by {100} facets by adding sodium citrate (Na(3)CA) and poly(vinyl pyrrolidone) (PVP), respectively, as a capping agent while all other parameters were kept the same. This research not only offers new insights into the role played by a capping agent in shape-controlled synthesis but also provides, for the first time, Ag octahedrons as small as 40 nm in edge length for optical and spectroscopic studies.

Conversion Reaction Mechanisms in Lithium Ion Batteries: Study of the Binary Metal Fluoride Electrodes

Materials that undergo a conversion reaction with lithium (e.g., metal fluorides MF(2): M = Fe, Cu, ...) often accommodate more than one Li atom per transition-metal cation, and are promising candidates for high-capacity cathodes for lithium ion batteries. However, little is known about the mechanisms involved in the conversion process, the origins of the large polarization during electrochemical cycling, and why some materials are reversible (e.g., FeF(2)) while others are not (e.g., CuF(2)). In this study, we investigated the conversion reaction of binary metal fluorides, FeF(2) and CuF(2), using a series of local and bulk probes to better understand the mechanisms underlying their contrasting electrochemical behavior. X-ray pair-distribution-function and magnetization measurements were used to determine changes in short-range ordering, particle size and microstructure, while high-resolution transmission electron microscopy (TEM) and electron energy-loss spectroscopy (EELS) were used to measure the atomic-level structure of individual particles and map the phase distribution in the initial and fully lithiated electrodes. Both FeF(2) and CuF(2) react with lithium via a direct conversion process with no intercalation step, but there are differences in the conversion process and final phase distribution. During the reaction of Li(+) with FeF(2), small metallic iron nanoparticles (<5 nm in diameter) nucleate in close proximity to the converted LiF phase, as a result of the low diffusivity of iron. The iron nanoparticles are interconnected and form a bicontinuous network, which provides a pathway for local electron transport through the insulating LiF phase. In addition, the massive interface formed between nanoscale solid phases provides a pathway for ionic transport during the conversion process. These results offer the first experimental evidence explaining the origins of the high lithium reversibility in FeF(2). In contrast to FeF(2), no continuous Cu network was observed in the lithiated CuF(2); rather, the converted Cu segregates to large particles (5-12 nm in diameter) during the first discharge, which may be partially responsible for the lack of reversibility in the CuF(2) electrode.

Tetragonal-to-Orthorhombic Structural Phase Transition at 90 K in the Superconductor Fe1.01Se

In this letter we show that superconducting Fe1.01Se undergoes a structural transition at 90 K from a tetragonal to an orthorhombic phase but that non-superconducting Fe1.03Se does not. Further, high resolution electron microscopy study at low temperatures reveals an unexpected additional modulation of the crystal structure of the superconducting phase involving displacements of the Fe atoms, and that the non-superconducting material shows a distinct, complex nanometer-scale structural modulation. Finally, we show that magnetism is not the driving force for the phase transition in the superconducting phase.

Fast phase unwrapping algorithm for interferometric applications.

A wide range of interferometric techniques recover phase information that is mathematically wrapped on the interval (-pi, pi). Obtaining the true unwrapped phase is a longstanding problem. We present an algorithm that solves the phase unwrapping problem, using a combination of Fourier techniques. The execution time for our algorithm is equivalent to the computation time required for performing eight fast Fourier transforms and is stable against noise and residues present in the wrapped phase. We have extended the algorithm to handle data of arbitrary size. We expect the state of the art of existing interferometric applications, including the possibility for real-time phase recovery, to benefit from our algorithm.

Tracking lithium transport and electrochemical reactions in nanoparticles

Expectations for the next generation of lithium batteries include greater energy and power densities along with a substantial increase in both calendar and cycle life. Developing new materials to meet these goals requires a better understanding of how electrodes function by tracking physical and chemical changes of active components in a working electrode. Here we develop a new, simple in-situ electrochemical cell for the transmission electron microscope and use it to track lithium transport and conversion in FeF(2) nanoparticles by nanoscale imaging, diffraction and spectroscopy. In this system, lithium conversion is initiated at the surface, sweeping rapidly across the FeF(2) particles, followed by a gradual phase transformation in the bulk, resulting in 1-3 nm iron crystallites mixed with amorphous LiF. The real-time imaging reveals a surprisingly fast conversion process in individual particles (complete in a few minutes), with a morphological evolution resembling spinodal decomposition. This work provides new insights into the inter- and intra-particle lithium transport and kinetics of lithium conversion reactions, and may help to pave the way to develop high-energy conversion electrodes for lithium-ion batteries.