Ning Lun

Large scale synthesis and gas-sensing properties of anatase TiO2 three-dimensional hierarchical nanostructures.

Three-dimensional (3D) crystalline anatase titanium dioxide (TiO(2)) hierarchical nanostructures were synthesized through a facile and controlled hydrothermal and after-annealing process. The formation mechanism for the anatase TiO(2) 3D hierarchical nanostructures was investigated in detail. The 3D hierarchical nanostructures morphologies are formed by self-organization of several tens of radially distributed thin petals with a thickness of several nanometers with a larger surface area. The surface area of TiO(2) hierarchical nanostructures determined by the Brunauer-Emmett-Teller (BET) adsorption isotherms was measured to be 64.8 m(2) g(-1). Gas sensing properties based on the hierarchical nanostructures were investigated. A systematic study on sensitivity as a function of temperatures and gas concentrations was carried out. It reveals an improved ethanol gas sensing response property with a sensitivity of about 6.4 at 350 degrees C upon exposure to 100 ppm ethanol vapor for the TiO(2) hierarchical nanostructures. A gas sensing mechanism based on the adsorption-desorption of oxygen on the surface of TiO(2) is discussed and analyzed. This novel gas sensor can be multifunctional and promising for practical applications. Furthermore, the hierarchical nanostructures with high surface area can find variety of potential applications such as solar cells, biosensors, catalysts, etc.

Sol-gel growth of hexagonal faceted ZnO prism quantum dots with polar surfaces for enhanced photocatalytic activity.

The hexagonal faceted ZnO quantum dots (QDs) about 3-4 nm have been prepared via a sol-gel route by using oleic acid (OA) as the capping agent. It is revealed by electron diffraction patterns and high resolution transmission electron microscopy lattice images that the profile surfaces of the highly crystalline ZnO QDs are mainly composed of {100} planes, with the Zn-terminated (001) faces and the opposite (001) faces presented as polar planes. Compared with spherical ZnO QDs, the hexagonal faceted ZnO QDs show enhanced photocatalytic activity for photocatalytic decomposition of methylene blue. A mechanism for the enhanced photocatalytic activity of the hexagonal faceted ZnO QDs for degradation of methylene blue is proposed. In addition to the large specific surface areas due to small size and high crystalline, the enhanced photocatalytic activity can mainly be ascribed to the special hexagonal morphology. The Zn-terminated (001) and O-terminated (001) polar faces are facile to adsorb oxygen molecules and OH(-) ions, resulting in a greater production rate of H(2)O(2) and OH(*) radicals, hence promoting the photocatalysis reaction. The synthesized hexagonal-shaped ZnO QDs with high photocatalytic efficiency will find widespread potential applications in environmental and biological fields.

Platinum-Nanoparticle-Modified TiO2 Nanowires with Enhanced Photocatalytic Property

Highly crystalline Pt nanoparticles with an average diameter of 5 nm were homogeneously modified on the surfaces of TiO(2) nanowires (Pt-TiO(2) NWs) by a simple hydrothermal and chemical reduction route. Photodegradation of methylene blue (MB) in the presence of Pt-TiO(2) NWs indicates that the photocatalytic activity of TiO(2) NWs can be greatly enhanced by Pt nanoparticle modification. The physical chemistry process and photocatalytic mechanism for Pt-TiO(2) NWs hybrids degrading MB were investigated and analyzed. The Pt attached on TiO(2) nanowires induces formation of a Schottky barrier between TiO(2) and Pt naonoparticles, leading to a fast transport of photogenerated electrons to Pt particles. Furthermore, Pt incoporation on TiO(2) surface can accelerate the transfer of electrons to dissolved oxygen molecules. Besides enhancing the electron-hole separation and charge transfer to dissolved oxygen, Pt may also serve as an effective catalyst in the oxidation of MB. However, a high Pt loading value does not mean a high photocatalytic activity. Higher content loaded Pt nanoparticles can absorb more incident photons which do not contribute to the photocatalytic efficiency. The highest photocatalytic activity for the Pt-TiO(2) nanohybrids on MB can be obtained at 1 at % Pt loading.

In situ synthesis of one-dimensional MWCNT/SiC porous nanocomposites with excellent microwave absorption properties

One-dimensional multiwalled carbon nanotube (MWCNT)/SiC porous nanocomposites were prepared via an in situ reaction between Si and MWCNTs induced by the reaction between Na and I2. The as-prepared nanocomposites exhibit outstanding microwave absorbing performances with an absorber thickness of about 2 mm. The absorbing bandwidth for the nanocomposites increases by raising the reaction temperature from 200 to 400 °C. The dielectric polarizations, which originate from the synergistic effect of the defects, porous structures and nanoparticles in the nanocomposites, are responsible for the excellent microwave absorbing performances.

Yttrium-modified Li4Ti5O12 as an effective anode material for lithium ion batteries with outstanding long-term cyclability and rate capabilities

Yttrium-modified Li4Ti5O12 (YLTO) was fabricated by a coprecipitation method using tetrabutyl titanate, Y(NO3)3·6H2O and LiOH·H2O as reactants, followed by simply sintering the dried mixture at 600 °C. The products and their lithiation–delithiation process were characterized by a combination of electrochemical measurements, X-ray diffraction, transmission electron microscopy and nitrogen adsorption. The YLTO exhibits excellent long-term cycling stability (over 1000 cycles) at a high current rate of 10 C and outstanding rate capabilities. Particularly, the YLTO demonstrates remarkable cyclability even if directly cycled at a rate of 10 C without low-rate activation and with no relaxation between charge and discharge. Even without utilizing carbon black as conductive material, the YLTO still shows prominent rate capabilities and long-term cyclic performance at a rate of 5 C. The excellent performance is ascribed to the increased lattice constant, improved electronic and ionic conductivities, refined grains with large surface area and uniform nanopores resulting from the Y-modification.

Excellent long-term cycling stability of La-doped Li4Ti5O12 anode material at high current rates

La-doped Li4Ti5O12 (LLTO) was prepared by a simple approach using tetrabutyl titanate, LiOH·H2O and La(NO3)3·6H2O as raw materials, followed by sintering the dried mixture at 600 °C for 5 h. Without requiring any further treatments, the as-obtained LLTO could exhibit excellent long-term cycling stability, high coulombic efficiency close to 100% at various charge–discharge rates, outstanding capacity retention at high current rates of 10–50 C, remarkable performance in the temperature range from −40 to 60 °C, good cycling performance even subjected to overcharging to about 10 times of the reversible capacity. The La-doped LTO could be directly used as efficient anode materials for lithium-ion batteries.

Carbon-coated Fe-Mn-O composites as promising anode materials for lithium-ion batteries.

Fe-Mn-O composite oxides with various Fe/Mn molar ratios were prepared by a simple coprecipitation method followed by calcining at 600 °C, and carbon-coated oxides were obtained by pyrolyzing pyrrole at 550 °C. The cycling and rate performance of the oxides as anode materials are greatly associated with the Fe/Mn molar ratio. The carbon-coated oxides with a molar ratio of 2:1 exhibit a stable reversible capacity of 651.8 mA h g(-1) at a current density of 100 mA g(-1) after 90 cycles, and the capacities of 567.7, 501.3, 390.7, and 203.8 mA h g(-1) at varied densities of 200, 400, 800, and 1600 mA g(-1), respectively. The electrochemical performance is superior to that of single Fe3O4 or MnO prepared under the same conditions. The enhanced performance could be ascribed to the smaller particle size of Fe-Mn-O than the individuals, the mutual segregation of heterogeneous oxides of Fe3O4 and MnO during delithiation, and heterogeneous elements of Fe and Mn during lithiation.

Enhanced electrochemical performance of FeWO4 by coating nitrogen-doped carbon.

FeWO4 (FWO) nanocrystals were prepared at 180 °C by a simple hydrothermal method, and carbon-coated FWO (FWO/C) was obtained at 550 °C using pyrrole as a carbon source. The FWO/C obtained from the product hydrothermally treated for 5 h exhibits reversible capacities of 771.6, 743.8, 670.6, 532.6, 342.2, and 184.0 mAh g(-1) at the current densities of 100, 200, 400, 800, 1600, and 3200 mA g(-1), respectively, whereas that from the product treated for 0.5 h achieves a reversible capacity of 205.9 mAh g(-1) after cycling 200 times at a current density of 800 mA g(-1). The excellent electrochemical performance of the FWO/C results from the combination of the nanocrystals with good electron transport performance and the nitrogen-doped carbon coating.

Microwave absorption properties of MWCNT-SiC composites synthesized via a low temperature induced reaction

The composites containing SiC and multiwalled carbon nanotubes (MWCNTs) were synthesized via the reaction of Si powders and MWCNTs induced by that of Na and sulfur. The MWCNT-SiC composites prepared at 600 °C exhibit excellent microwave absorbing properties, which reach a minimum reflection loss of -38.7 dB at a frequency around 12.9 GHz. The absorbing properties are bound up with the high yield of porous SiC spheres comprised of nanocrystals. The porous structure, high density of stacking faults in SiC crystallites, interfaces between MWCNTs and SiC spheres, grain boundaries between SiC nanocrystals, as well as the interfacial polarizations aroused therefrom, are responsible for the excellent microwave absorbing properties.

Ionic Conductor of Li2SiO3 as an Effective Dual-Functional Modifier To Optimize the Electrochemical Performance of Li4Ti5O12 for High-Performance Li-Ion Batteries

Ionic conductor of Li2SiO3 (LSO) was used as an effective modifier to fabricate surface-modified Li4Ti5O12 (LTO) via simply mixing followed by sintering at 750 °C in air. The electrochemical performance of LTO was enhanced by merely adjusting the mass ratio of LTO/LSO, and the LTO/LSO composite with 0.51 wt % LSO exhibited outstanding rate capabilities (achieving reversible capacities of 163.8, 157.6, 153.1, 147.0, and 137.9 mAh g-1 at 100, 200, 400, 800, and 1600 mA g-1, respectively) and remarkable long-term cycling stability (120.2 mAh g-1 after 2700 cycles with a capacity fading rate of only 0.0074% per cycle even at 500 mA g-1). Combining structural characterization with electrochemical analysis, the LSO coating coupled with the slight doping effect adjacent to the LTO surface contributes to the enhancement of both electronic and ionic conductivities of LTO.