Jun Jie Niu

Two-Dimensional Nanocrystals Produced by Exfoliation of Ti(3)AlC(2)

Currently, however, there are relatively few such atomically layered solids. [ 2–5 ] Here, we report on 2D nanosheets, composed of a few Ti 3 C 2 layers and conical scrolls, produced by the room temperature exfoliation of Ti 3 AlC 2 in hydrofl uoric acid. The large elastic moduli predicted by ab initio simulation, and the possibility of varying their surface chemistries (herein they are terminated by hydroxyl and/or fl uorine groups) render these nanosheets attractive as polymer composite fi llers. Theory also predicts that their bandgap can be tuned by varying their surface terminations. The good conductivity and ductility of the treated powders suggest uses in Li-ion batteries, pseudocapacitors, and other electronic applications. Since Ti 3 AlC 2 is a member of a 60 + group of layered ternary carbides and nitrides known as the MAX phases, this discovery opens a door to the synthesis of a large number of other 2D crystals. Arguably the most studied freestanding 2D material is graphene, which was produced by mechanical exfoliation into single-layers in 2004. [ 1 ] Some other layered materials, such as hexagonal BN, [ 2 ] transition metal oxides, and hydroxides, [ 4 ] as well as clays, [ 3 ] have also been exfoliated into 2D sheets. Interestingly, exfoliated MoS 2 single layers were reported as early as in 1986. [ 5 ] Graphene is fi nding its way to applications ranging from supercapacitor electrodes [ 6 ] to reinforcement in composites. [ 7 ] Although graphene has attracted more attention than all other 2D materials combined, its simple chemistry and the weak van der Waals bonding between layers in multilayer structures limit its use. Complex, layered structures that contain more than one element may offer new properties because they

Mechanical properties and biomineralization of multifunctional nanodiamond-PLLA composites for bone tissue engineering.

Multifunctional bone scaffold materials have been produced from a biodegradable polymer, poly(L-lactic acid) (PLLA), and 1-10% wt of octadecylamine-functionalized nanodiamond (ND-ODA) via solution casting followed by compression molding. By comparison to pure PLLA, the addition of 10% wt of ND-ODA resulted in a significant improvement of the mechanical properties of the composite matrix, including a 280% increase in the strain at failure and a 310% increase in fracture energy in tensile tests. The biomimetic process of bonelike apatite growth on the ND-ODA/PLLA scaffolds was studied using microscopic and spectroscopic techniques. The enhanced mechanical properties and the increased mineralization capability with higher ND-ODA concentration suggest that these biodegradable composites may potentially be useful for a variety of biomedical applications, including scaffolds for orthopedic regenerative engineering.

High-rate aluminium yolk-shell nanoparticle anode for Li-ion battery with long cycle life and ultrahigh capacity

Alloy-type anodes such as silicon and tin are gaining popularity in rechargeable Li-ion batteries, but their rate/cycling capabilities should be improved. Here by making yolk-shell nanocomposite of aluminium core (30 nm in diameter) and TiO2 shell (∼3 nm in thickness), with a tunable interspace, we achieve 10 C charge/discharge rate with reversible capacity exceeding 650 mAh g−1 after 500 cycles, with a 3 mg cm−2 loading. At 1 C, the capacity is approximately 1,200 mAh g−1 after 500 cycles. Our one-pot synthesis route is simple and industrially scalable. This result may reverse the lagging status of aluminium among high-theoretical-capacity anodes.

In Situ Observation of Random Solid Solution Zone in LiFePO4 Electrode

Nanostructured LiFePO4 (LFP) electrodes have attracted great interest in the Li-ion battery field. Recently there have been debates on the presence and role of metastable phases during lithiation/delithiation, originating from the apparent high rate capability of LFP batteries despite poor electronic/ionic conductivities of bulk LFP and FePO4 (FP) phases. Here we report a potentiostatic in situ transmission electron microscopy (TEM) study of LFP electrode kinetics during delithiation. Using in situ high-resolution TEM, a Li-sublattice disordered solid solution zone (SSZ) is observed to form quickly and reach 10-25 nm × 20-40 nm in size, different from the sharp LFP|FP interface observed under other conditions. This 20 nm scale SSZ is quite stable and persists for hundreds of seconds at room temperature during our experiments. In contrast to the nanoscopically sharp LFP|FP interface, the wider SSZ seen here contains no dislocations, so reduced fatigue and enhanced cycle life can be expected along with enhanced rate capability. Our findings suggest that the disordered SSZ could dominate phase transformation behavior at nonequilibrium condition when high current/voltage is applied; for larger particles, the SSZ could still be important as it provides out-of-equilibrium but atomically wide avenues for Li(+)/e(-) transport.

A novel self-cleaning coating with silicon carbide nanowires.

A novel self-cleaning glass was successfully achieved by coating macroscopical SiC nanowires (SiCNWs) in tetraethyl orthosilicate (TEOS) solution. The water contact angle (CA) was high, up to approximately 160 degrees, and the sliding angle was low, down to approximately 5 degrees, when SiCNWs were coated through 10 cycles, with a high roughness Ra of 1928.9 nm. High chemical stability was obtained even after immersing the sample in water for 14 days (336 h). The calculated data by using nano/micropillar composite structure model displayed a beneficial understanding on thehydrophobic property. The feasible coating on any substrate, high CA, and long lifetime make SiCNW a potential superhydrophobic material in various self-cleaning fields.

Preparation of graphitic carbon with high surface area and its application as an electrode material for fuel cells

Nanostructured graphitic carbon materials have wide applications. However, the synthesis of such materials with a high surface area is still a great challenge. In this study, graphitic carbon nanocages with a surface area as high as 400–800 m2 g−1 were synthesized by pyrolysis of ethanol with dissolved iron carbonyl. This graphitic carbon was successfully applied as an electrode material for proton exchange membrane fuel cells and showed 40% improvement in fuel cell performance from amorphous carbon. The present method could be applied to large-scale production of graphitic carbon with a high surface area and would be practically relevant for fuel cell and many other technologies.

Nanowire liquid pumps

The ability to form tiny droplets of liquids and control their movements is important in printing or patterning, chemical reactions and biological assays. So far, such nanofluidic capabilities have principally used components such as channels, nozzles or tubes, where a solid encloses the transported liquid. Here, we show that liquids can flow along the outer surface of solid nanowires at a scale of attolitres per second and the process can be directly imaged with in situ transmission electron microscopy. Microscopy videos show that an ionic liquid can be pumped along tin dioxide, silicon or zinc oxide nanowires as a thin precursor film or as beads riding on the precursor film. Theoretical analysis suggests there is a critical film thickness of ∼10 nm below which the liquid flows as a flat film and above which it flows as discrete beads. This critical thickness is the result of intermolecular forces between solid and liquid, which compete with liquid surface energy and Rayleigh-Plateau instability.

Carbon nanotube-tipped endoscope for in situ intracellular surface-enhanced Raman spectroscopy.

Gold nanoparticle-decorated carbon nanotubes (CNTs) are used to study intracellular environments in situ using surface-enhanced Raman spectroscopy (SERS). CNTs are decorated with gold nanoparticles and assembled onto the tips of pulled glass capillaries to form a SERS-enabled endoscope. The sub-micrometer size and high mechanical strength of the endoscope make it possible to penetrate the cell membrane for intracellular probing and remain positioned inside during lengthy SERS measurements without causing damage to the cell. Using the SERS-enabled endoscope, DNA and other biomolecules are detected in situ within the nucleus of a single human cervical carcinoma cell in a minimally invasive manner. The SERS-enabled endoscopes exhibit high selectivity and sensitivity for detecting trace amounts of analytes (≈1 pM) in biofluid environments, highlighting their capabilities as label-free, biological sensors for real-time in situ cellular diagnostics, biological detection, and pharmaceutical research.

High Volumetric Capacity Three-Dimensionally Sphere-Caged Secondary Battery Anodes.

High volumetric energy density secondary batteries are important for many applications, which has led to considerable efforts to replace the low volumetric capacity graphite-based anode common to most Li-ion batteries with a higher energy density anode. Because most high capacity anode materials expand significantly during charging, such anodes must contain sufficient porosity in the discharged state to enable the expansion, yet not excess porosity, which lowers the overall energy density. Here, we present a high volumetric capacity anode consisting of a three-dimensional (3D) nanocomposite formed in only a few steps which includes both a 3D structured Sn scaffold and a hollow Sn sphere within each cavity where all the free Sn surfaces are coated with carbon. The anode exhibits a high volumetric capacity of ∼1700 mA h cm(-3) over 200 cycles at 0.5C, and a capacity greater than 1200 mA h cm(-3) at 10C. Importantly, the anode can even be formed into a commercially relevant ∼100 μm thick form. When assembled into a full cell the anode shows a good compatibility with a commercial LiMn2O4 cathode. In situ TEM observations confirm the electrode design accommodates the necessary volume expansion during lithiation.

Cutting of multi-walled carbon nanotubes by solid-state reaction

Current carbon nanotubes (CNT) are typically synthesized with micrometer lengths and low dispersion. In this study, a new approach is reported to cut the conventional long and entangled CNTs to short and dispersed ones with lengths of less than 200 nm. This was achieved by depositing NiO particles on CNTs first and then inducing a chemical reaction between them. The present cutting approach based on such a solid-state reaction has advantages of producing short CNTs with a narrow length distribution, high dispersion, and a low material loss over previous ones based on a gaseous or liquid-state reaction. Such short CNTs would fill the large gap between small spheroidal fullerenes and long CNTs and be of paramount scientific and technological importance in many fields such as electronics, diagnostics, pharmaceuticals, environmental and energy industries.