Xuanhui Qu

Hollow core-shell structured Si/C nanocomposites as high-performance anode materials for lithium-ion batteries.

Hollow core-shell structured Si/C nanocomposites were prepared to adapt for the large volume change during a charge-discharge process. The Si nanoparticles were coated with a SiO2 layer and then a carbon layer, followed by etching the interface SiO2 layer with HF to obtain hollow core-shell structured Si/C nanocomposites. The Si nanoparticles are well encapsulated in a carbon matrix with an internal void space between the Si core and the carbon shell. The hollow core-shell structured Si/C nanocomposites demonstrate a high specific capacity and excellent cycling stability, with capacity decay as small as 0.02% per cycle. The enhanced electrochemical performance can be attributed to the fact that the internal void space can accommodate the volume expansion of Si during lithiation, thus preserving the structural integrity of electrode materials, and the carbon shell can increase the electronic conductivity of the electrode.

Research on electrochemical characteristics and microstructure of Mm(NiMnAl)4.9Co0.2 rapidly quenched alloy

Abstract The cycling stability of low-Co hydrogen storage alloy was improved by rapid quenching. A low-Co hydrogen storage alloy with outstanding properties was obtained with a content of Co as low as 2.7 wt.%. It was first found that the quenching rate could affect the discharge capacity of the alloy: when the quenching rate was lower than 10 m/s, rapid quenching increased the discharge capacity and when the quenching rate was higher than 15 m/s, it significantly decreased the discharge capacity. In addition, the cycle life of the Mm(NiMnAl) 4.9 Co 0.2 alloy could not be increased when the quenching rate was lower than 10 m/s, but instead, its cycle life was lowered to less than that of the as-cast alloy. The microstructures of the alloy were investigated by XRD and TEM in order to understand and explain these special properties.

Research of low-Co AB5 type rare-earth-based hydrogen storage alloy electrodes

Abstract In order to further reduce the cost of AB 5 type rare-earth-based hydrogen storage alloy, a low-Co AB 5 type hydrogen storage alloy was prepared by substituting Cr, Si, Cu for Co and adjusting of the composition. The result showed that the effect of the three kinds of substituting elements on cycle life increased in the sequence Si>Cr>Cu; and on the discharge capacity in the sequence Cu>Cr>Si. An overall favorable effect becomes possible by adding small quantities of Cr, Cu, Si. The discharge capacity and activation property as well as rate discharge capability of low-Co mischmetal based hydrogen storage electrode alloy reached the requirements of practical use when applying nonstoichiometric compositions.

Constructing water-resistant CH3NH3PbI3 perovskite films via coordination interaction

Organic–inorganic halide CH3NH3PbI3 (MAPbI3) perovskite solar cells (PSCs) have attracted intensive attention due to their high power conversion efficiency and low fabrication cost. However, MAPbI3 is known to be very sensitive to humidity, and the intrinsic long-term stability of the MAPbI3 film remains a critical challenge. 2-Aminoethanethiol (2-AET) was used as a ligand to bridge the organic compound (MAI) and inorganic compound (PbI2), which restricted the fast growth of PbI2 to realize the synchronous growth environment of MAI and PbI2 crystals, resulting in the formation of a compact MAPbI3 film with polygonal grains. Due to the compact (PbI2)–2-AET–(MAI) molecule barrier layers in the MAPbI3 structure, the resulting perovskite films showed excellent intrinsic water-resistance, with the MAPbI3 perovskite crystal structure retained for a long time (>10 minutes) after immersion in water. This work makes a step towards obtaining long-term stable MAPbI3 perovskite devices.

Synthesis of novel ZnV2O4 spinel oxide nanosheets and their hydrogen storage properties

We report the synthesis of ZnV2O4 spinel oxide novel nanosheets via a template free route to explore its potential hydrogen storage properties for the first time. 2D layered nanostructures are excellent candidates for storage applications. This attracted our interest to synthesize novel spinel oxide nanosheets (NSNs) of ZnV2O4. The maximum value for hydrogen absorption in ZnV2O4 nanosheets at 473 K is 1.36 wt.% and 1.74 wt.% at 573 K, respectively. Our hydrogen storage measurements along ZnV2O4 reveal its superiority over previous reports on hydrogen absorption values concerning oxides, nitrides and chalcogenides. To understand the rate-limiting mechanism, various kinetics models are applied. The calculations show that kinetics is governed by 3D growth with constant interface velocity. The measurements point to ZnV2O4 spinel oxide as a promising hydrogen storage material. PL measurements demonstrate the potential for violet/blue optoelectronic devices.

Preparation and properties of porous Ti–10Mo alloy by selective laser sintering

In this study, porous Ti-10Mo alloy was prepared from a mixture of titanium, molybdenum and epoxy resin powders by selective laser sintering preforming, debinding and sintering at 1200 °C under a pure argon atmosphere. The influence of sintering process on the porous, microstructural and mechanical properties of the porous alloy was discussed. The results indicate that the pore characteristic parameters and mechanical properties mainly depend on the holding time at 1200 °C, except that the maximum strain keeps at about 45%. The matrix microstructure is dominated by α phase with a small quantity of β phase at room temperature. As the holding time lengthens from 2 to 6h, the average pore size and the porosity decrease from 180 to 50 μm and from 70 to 40%, respectively. Meanwhile, the Youngs modulus and the compressive yield strength increase in the ranges of 10-20 GPa and 180-260 MPa, respectively. Both the porous structure and the mechanical properties of the porous Ti-10Mo alloy can be adjusted to match with those of natural bone.

Enhanced hydrogen storage properties of LiAlH4 catalyzed by CoFe2O4 nanoparticles

The catalytic effects of CoFe2O4 nanoparticles on the hydrogen storage properties of LiAlH4 prepared by ball milling were investigated. The onset desorption temperature of the LiAlH4 + 2 mol% CoFe2O4 sample is 65 °C, which is 90 °C lower that of the as-received LiAlH4, with approximately 7.2 wt% hydrogen released at 250 °C. The isothermal desorption results show that for the 2 mol% CoFe2O4 doped sample dehydrogenated at 120 °C, 6.8 wt% of hydrogen can be released within 160 min, which is 6.1 wt% higher than that of the as-received LiAlH4 under the same conditions. Through the differential scanning calorimetry (DSC) and the Kissinger desorption kinetics analyses, the apparent activation energy, Ea, of the 2 mol% CoFe2O4 doped sample is calculated as 52.4 kJ mol−1 H2 and 86.5 kJ mol−1 H2 for the first two decomposition processes. This is 42.4 kJ mol−1 H2 and 86.1 kJ mol−1 H2 lower compared with the pristine LiAlH4, respectively, indicating considerably improved dehydrogenation kinetics by doping the CoFe2O4 catalyst in the LiAlH4 matrix. From the Fourier transform infrared spectroscopy (FTIR) and X-ray diffraction (XRD) analyses, a series of finely dispersed Fe and Co species with a range of valence states, produced from the reactions between LiAlH4 and CoFe2O4, play a synergistic role in remarkably improving LiAlH4 dehydrogenation properties. The rehydrogenation properties of the LiAlH4 + 2 mol% CoFe2O4 sample have also been investigated at 140 °C under 6.5 MPa pressure held for 2.5 h.

Combustion synthesis and excellent photocatalytic degradation properties of W18O49

In this paper, one-dimensional W18O49 nanopowders were fabricated by a one-step solution combustion method using glycine as the fuel and a metal acid radical ion as the metal source. The morphologies and non-stoichiometric single-crystal phase of W18O49 can be controlled by changing the amount of the fuel. The nanoneedles had a large amount of defects such as oxygen vacancies. This characteristic resulted in an excellent visible light-driven photocatalytic performance that took about 50 min to degrade methylene blue (100 mL; 40 mg L−1) under visible light. The interesting reaction mechanism of such needle-like W18O49 and the photocatalytic mechanism are studied in this paper.

Morphology and microstructure characterization of 95W-3.5Ni-1.5Fe powder prepared by mechanical alloying

Abstract The mechanism of mechanical solid-state reactions for formation of tungsten heavy alloy powder was discussed. A high-energy ball mill operating at room temperature was used for preparing tungsten heavy alloy powders, starting from elemental tungsten (W), nickel (Ni), and iron (Fe) powders. X-ray diffraction (XRD), particle size analyzer, scanning electron microscopy (SEM), and transmission electron microscopy (TEM) were used to follow the progress of the mechanical solid-state reaction of W, Ni, and Fe powders. These morphological studies revealed three stages in the milling process. In the first stage, the particle deformation changes the irregular structure of the as-received powder particles to flattened morphology, and the average particle size increases. In the second stage, the powder is sufficiently deformed and the tendency to fracture predominates over welding, and the particle size decreases. With continuous milling, the system reaches steady state, and relatively small and uniform particle size distribution is obtained after 20 h of milling.

Synthesis of Mesoporous Single Crystal Co(OH)2 Nanoplate and Its Topotactic Conversion to Dual-Pore Mesoporous Single Crystal Co3O4

A new class of mesoporous single crystalline (MSC) material, Co(OH)2 nanoplates, is synthesized by a soft template method, and it is topotactically converted to dual-pore MSC Co3O4. Most mesoporous materials derived from the soft template method are reported to be amorphous or polycrystallined; however, in our synthesis, Co(OH)2 seeds grow to form single crystals, with amphiphilic block copolymer F127 colloids as the pore producer. The single-crystalline nature of material can be kept during the conversion from Co(OH)2 to Co3O4, and special dual-pore MSC Co3O4 nanoplates can be obtained. As the anode of lithium-ion batteries, such dual-pore MSC Co3O4 nanoplates possess exceedingly high capacity as well as long cyclic performance (730 mAh g(-1) at 1 A g(-1) after the 350th cycle). The superior performance is because of the unique hierarchical mesoporous structure, which could significantly improve Li(+) diffusion kinetics, and the exposed highly active (111) crystal planes are in favor of the conversion reaction in the charge/discharge cycles.