Anode-Free Aqueous Aluminum Ion Batteries.

Aqueous aluminum ion batteries (AAIBs) possess the advantages of high safety, cost-effectiveness, eco-friendliness and high theoretical capacity. However, the Al2O3 film on the Al anode surface, a natural physical barrier to the plating of hydrated aluminum ions, is a key factor in the decomposition of the aqueous electrolyte and the severe hydrogen precipitation reaction. To circumvent the obnoxious Al anode, a proof-of-concept of an anode-free AAIB is first proposed, in which Al2TiO5, as a cathode pre-aluminum additive (Al source), can replenish Al loss by over cycling. The Al-Cu alloy layer, formed by plating Al on the Cu foil surface during the charge process, possesses a reversible electrochemical property and is paired with a polyaniline (cathode) to stimulate the battery to exhibit high initial discharge capacity (175 mAh g-1), high power density (≈410 Wh L-1) and ultra-long cycle life (4000 cycles) with the capacity retention of ≈60% after 1000 cycles. This work will act as a primer to ignite the enormous prospective researches on the anode-free aqueous Al ion batteries.

Cobalt-Catalyzed Efficient Convergent Asymmetric Hydrogenation of E/Z-Enamides.

Using the diphosphine-cobalt-zinc catalytic system, an efficient asymmetric hydrogenation of internal simple enamides has been realized. In particular, the Ph-BPE ligand can achieve convergent asymmetric hydrogenation of E/Z-substrates. High yields and excellent enantioselectivities were obtained for both acyclic and cyclic enamides bearing α-alkyl-ß-aryl, α-aryl-ß-aryl, and α-aryl-ß-alkyl substituents. Hydrogenated products can be applied for the synthesis of useful chiral drugs such as Arfromoterol, Rotigotine, and Norsertraline. In addition, reasonable catalytic mechanism and stereocontrol mode are proposed based on DFT calculations.

Nanocoating covalent organic frameworks on nickel nanowires for greatly enhanced-performance supercapacitors.

Nanocoatings of covalent organic frameworks (COFs) on nickel nanowires (NiNWs) have been designed and successfully fabricated for the first time, which showed greatly enhanced electrochemical performances for supercapacitors. The specific capacitance of electrodes based on as-fabricated COFs nanocoatings reached up to 314 F g-1 at 50 A g-1, which retained 74% of the specific capacitance under the current density of 2 A g-1. The ultrahigh current density makes the charge-discharge process extremely rapid. The outstanding electrochemical performances of COFs nanocoating on NiNWs make it an ideal candidate for supercapacitors. And the nanocoating-design can also give a guidance for application of COFs in high-performance energy storages.

Carbon Nanotube-Based Chemiresistive Sensors.

The development of simple and low-cost chemical sensors is critically important for improving human life. Many types of chemical sensors have been developed. Among them, the chemiresistive sensors receive particular attention because of their simple structure, the ease of high precise measurement and the low cost. This review mainly focuses on carbon nanotube (CNT)-based chemiresistive sensors. We first describe the properties of CNTs and the structure of CNT chemiresistive sensors. Next, the sensing mechanism and the performance parameters of the sensors are discussed. Then, we detail the status of the CNT chemiresistive sensors for detection of different analytes. Lastly, we put forward the remaining challenges for CNT chemiresistive sensors and outlook the possible opportunity for CNT chemiresistive sensors in the future.

Controlled growth of conical nickel oxide nanocrystals and their high performance gas sensing devices for ammonia molecule detection.

NiO nanocones with good symmetry and highly ordered structure on NiO foil substrate have been successfully fabricated via a facile wet chemical approach combined with subsequent high temperature oxidation. These organized conical superstructures grow only along a certain direction and be controlled via the self-assembly and oriented attachment of a nucleus, which mainly rely on the similar surface energies and the extent of lattice matching of the oriented attached surfaces. During high temperature oxidation, the electric field created via the Ni(2+) and O(2-) facilitates Ni(2+) diffusion outward along the grain boundaries and O(2-) diffusion inward toward to meet the Ni(2+) ions, forming NiO. The as-grown NiO nanocones are 50-350 nm in diameter and 50-400 nm in height. The tip diameter of the nanocone is about 30 nm and the apex angle of the nanocone is about 40°. Meanwhile, we systematically investigated the gas sensing properties of the sensors based on the as-fabricated NiO foil covered with nanocone arrays for ammonia detection at room temperature. The results show that the gas sensing devices have outstanding sensitivity, reproducibility and selectivity, which are mainly because of the excellent connection between the NiO sensing materials and the Au electrodes, the strong electron donating ability of ammonia and the large active surface of selective physisorption for ammonia.

Cobalt-Catalyzed Enantioselective Reductive Amination of Ketones with Hydrazides.

An efficient cobalt-catalyzed asymmetric reductive amination of ketones with hydrazides has been realized, directly producing valuable chiral hydrazines in high yields and enantioselectivities (up to 98% enantiomeric excess).

Zn(x)Cd(1-x)Se nanomultipods with tunable band gaps: synthesis and first-principles calculations.

In this paper, we demonstrate that ZnxCd1-xSe nanomultipods can be synthesized via a facile and nontoxic solution-based method. Interesting aspects of composition, morphology and optical properties were deeply explored. The value of Zn/(Zn+Cd) could be altered across the entire range from 0.08 to 0.86 by varying the ratio of cation precursor contents. The band gap energy could be linearly tuned from 1.88 to 2.48 eV with respect to the value of Zn/(Zn+Cd). The experiment also showed that oleylamine played a dominant role in the formation of multipod structure. A possible growth mechanism was further suggested. First-principles calculations of band gap energy and density of states in the Vienna ab initio simulation package code were performed to verify the experimental variation tendency of the band gap. Computational results indicated that dissimilarities of electronic band structures and orbital constitutions determined the tunable band gap of the as-synthesized nanomultipod, which might be promising for versatile applications in relevant areas of solar cells, biomedicine, sensors, catalysts and so on.

Graphene oxide reinforced polyimide nanocomposites via in situ polymerization.

Graphene oxide (GO) reinforced polyimide nanocomposites were synthesized by in situ polymerization of monomers in the presence of GO sheets dispersed in N,N-Dimethylacetamide (DMAc). The functional groups (e.g., hydroxyl, epoxide, and carboxyl groups) associated with the GO make GO excellent dispersion in the organic solvent, which benefits the subsequent in situ polymerization. This process enabled uniform dispersion of GO sheets in the polymer matrix. The resultant GO-polyimide nanocomposite films were studied by tensile test, TGA and SEM. The results showed that the GO sheets incorporated in the polymer matrix exhibited a layer-aligned structure without destruction of the thermal stability of the polymer matrix, and a loading of GO (10 wt%) resulted in a significant enhancement in elastic modulus (86.4%).

Hole doping and surface functionalization of single-walled carbon nanotube chemiresistive sensors for ultrasensitive and highly selective organophosphor vapor detection.

We developed a chemiresistive sensor based on doped and functionalized semiconducting single-walled carbon nanotube (SWNT) networks for ultrasensitive and rapid detection of dimethyl methylphosphonate (DMMP) (simulant of nerve agent sarin) vapor. The semiconducting SWNT network was deposited between interdigitated electrodes and modified by solid organic acid tetrafluorohydroquinone (TFQ). The TFQ molecules could not only selectively bind DMMP onto the sidewalls of SWNTs via the strong hydrogen bonding interaction, but also tailor the electronic properties of SWNTs via heavy hole doping. This synergetic effect significantly improved the sensitivity of the devices, and enabled the sensors to easily detect DMMP at 20 parts-per-trillion (ppt) concentration with a response time of less than 2 min, without the need for pre-concentration of the analytes. This sensitivity is about five orders of magnitude higher than that of the unmodified SWNT chemiresistor, and also significantly higher than that of the functionalized SWNT chemiresistors previously reported. Moreover, the SWNT-TFQ sensors could be recovered when DMMP is replaced with referencing gas. The SWNT-TFQ sensors also show excellent selectivity toward DMMP over some interfering organic vapors. The response mechanism, i.e. charge transfer and dedoping was investigated.

Hexafluorobisphenol A covalently functionalized single-walled carbon nanotubes for detection of dimethyl methylphosphonate vapor.

Hexafluorobisphenol A (6FBPA), as a novel nerve agents sensing molecule, has been successfully attached onto the surface of single-walled carbon nanotubes (SWNTs). The sensing groups have been confirmed by infrared spectroscopy, Raman spectroscopy and X-ray photoelectron spectrometry. The results revealed that the sensing groups had been successfully anchored on the surface of nanotubes. The quantitative determination of the functional groups has also been carried out through characterization by thermogravimetric analysis. Furthermore, the morphology of the resultant SWNT-6FBPA hybrids has been observed by transmission electron microscopy and scanning electron microscopy. Due to the existence of phenolic hydroxyl groups, which can form strong hydrogen-bonding with dimethyl methylphosphonate (DMMP) (simulant of nerve agent sarin), the functionalized SWNTs showed excellent sensitivity and selectivity while the sensing devices have been fabricated.

Synthesis and Stability of Hydrogen Storage Material Aluminum Hydride.

Aluminum hydride (AlH3) is a binary metal hydride with a mass hydrogen density of more than 10% and bulk hydrogen density of 148 kg H2/m3. Pure aluminum hydride can easily release hydrogen when heated. Due to the high hydrogen density and low decomposition temperature, aluminum hydride has become one of the most promising hydrogen storage media for wide applications, including fuel cell, reducing agents, and rocket fuel additive. Compared with aluminum powder, AlH3 has a higher energy density, which can significantly reduce the ignition temperature and produce H2 fuel in the combustion process, thus reducing the relative mass of combustion products. In this paper, the research progress about the structure, synthesis, and stability of aluminum hydride in recent decades is reviewed. We also put forward the challenges for application of AlH3 and outlook the possible opportunity for AlH3 in the future.

Vinyltriethoxysilane crosslinked poly(acrylic acid sodium) as a polymeric binder for high performance silicon anodes in lithium ion batteries.

In order to effectively relieve the large volume changes of silicon anodes during the cycling process in lithium ion batteries (LIBs), we developed a vinyltriethoxysilane crosslinked poly(acrylic acid sodium) polymeric binder (PVTES-NaPAA) for the Si anodes. The PVTES-NaPAA binder was synthesized by using a free radical co-polymerization method with VTES and NaPAA as precursors. In this binder, NaPAA with carboxyl groups can provide strong adhesion between Si particles and the current collector. Furthermore, VTES can be hydrolyzed and condense with each other to form a three-dimensional crosslinked network; the special network makes it possible to improve the Si electrode stability, resulting in an excellent cycling performance (78.2% capacity retention after 100 cycles) and high coulombic efficiency (99.9% after 100 cycles).

Covalent sidewall functionalization of single-walled carbon nanotubes: a photoreduction approach.

Covalent sidewall functionalization of single-walled carbon nanotubes (SWNTs) via photoreduction of aromatic ketones by alcohols is reported for the first time. Irradiation of benzophenone, benzhydrol and SWNTs in benzene resulted in covalent attachment of benzhydrol to the sidewalls of the SWNTs. A variety of tools were used to characterize the functionalized SWNTs. Raman scattering, UV-visible and near-IR spectroscopy confirm the covalent nature of the sidewall functionalization. Attenuated total reflection (ATR) FTIR and NMR provided evidence for attachment of benzhydrol onto the sidewalls of nanotubes. Thermogravimetric analysis (TGA) showed that the degree of functionalization was about one benzhydrol in 52 sidewall carbons. A long-chain hydrocarbon marker (n-C(18)H(35)) was also grafted onto the functional groups by esterification reaction for high-resolution TEM (HRTEM) visualization.

Serum concentrations of hyaluronic acid, procollagen type III NH2-terminal peptide, and laminin in patients with chronic congestive heart failure.

OBJECTIVE: To explore the role of serum fibrotic indices including hyaluronic acid (HA), procollagen type III NH2 -terminal peptide (PCIIIP), and laminin (LN) in assessing the severity of myocardial fibrosis in chronic congestive heart failure (CHF). METHODS: Serum levels of HA, PCIIIP, and LN in 39 patients with CHF [14 with New York Heart Association (NYHA) functional class II, 21 with class III, 4 with class IV] and in 46 patients with NYHA functional class I were assessed by radioimmunoassay. RESULTS: The serum concentrations of HA, PCIIIP, and LN were 359.75 +/- 84.59 microg/L, 77.88 +/- 24.67 microg/L, 86.73 +/- 23.90 microg/L in CHF group, and 211.60 +/- 54. 80 microg/L, 64.82 +/- 23.99 microg/L, 82.26 +/- 23.98 microg/L in NYHA functional class I group, respectively. The HA level was significantly higher in CHF patients as compared with NYHA functional class I group (P < 0.05). However, no difference was found in the levels of PCIIIP and LN between CHF group and NYHA functional class I group. The serum HA concentration was negatively correlated with left ventricular ejection fraction (r = - 0.71, P < 0.05). CONCLUSION: Serum HA level may act as an indicator for myocardial fibrosis.

Poly (acrylic acid sodium) grafted carboxymethyl cellulose as a high performance polymer binder for silicon anode in lithium ion batteries.

The design of novel binder systems is required for the high capacity silicon (Si) anodes which usually undergo huge volume change during the charge/discharge cycling. Here, we introduce a poly (acrylic acid sodium)-grafted-carboxymethyl cellulose (NaPAA-g-CMC) copolymer as an excellent binder for Si anode in lithium ion batteries (LIBs). The NaPAA-g-CMC copolymer was prepared via a free radical graft polymerization method by using CMC and acrylic acid as precursors. Unlike the linear, one-dimensional binders, the NaPAA-g-CMC copolymer binder is expected to present multi-point interaction with Si surface, resulting in enhanced binding ability with Si particles as well as with the copper (Cu) current collectors, and building a stable solid electrolyte interface (SEI) layer on the Si surface. The NaPAA-g-CMC based Si anode shows much better cycle stability and higher coulombic efficiency than those made with the well-known linear polymeric binders such as CMC and NaPPA.

Carbon nanotube intramolecular p-i-n junction diodes with symmetric and asymmetric contacts.

A p-i-n junction diode based on the selectively doped single-walled carbon nanotube (SWCNT) had been investigated, in which two opposite ends of individual SWCNT channel were doped into the p- and n-type SWCNT respectively while the middle segment of SWCNT was kept as the intrinsic. The symmetric and asymmetric contacts were used to fabricate the p-i-n junction diodes respectively and studied the effect of the contact on the device characteristics. It was shown that a low reverse saturation current of ~20 pA could be achieved by these both diodes. We found that the use of the asymmetric contact can effectively improve the performance of the p-i-n diode, with the rectification ratio enhanced from ~10(2) for the device with the Au/Au symmetric contact to >10(3) for the one with the Pd/Al asymmetric contact. The improvement of the device performance by the asymmetric-contact structure was attributed to the decrease of the effective Schottky-barrier height at the contacts under forward bias, increasing the forward current of the diode. The p-i-n diode with asymmetric contact also had a higher rectification ratio than its counterpart before doping the SWCNT channel, which is because that the p-i-n junction in the device decreased the reverse saturated current.

Hierarchical heterostructures based on prickly Ni nanowires/Cu2O nanoparticles with enhanced photocatalytic activity.

Metal-semiconductor-based photocatalysts show high efficiencies and catalytic activities in the photocatalysis process. Herein, the magnetic and one-dimensional Ni-Cu2O heteronanowires have been fabricated via in situ reduction of pre-adsorbed Cu(2+) on the surface of prickly Ni nanowires in an ethanol solution for photocatalysis application. The resultant Ni-Cu2O heteronanowires show higher photocatalytic ability than pure Cu2O nanoparticles in the degradation of methyl orange. The enhancement of photocatalytic efficiency can be ascribed to the unique one-dimensional nanostructure and the electron sink effect of Ni nanowires in the heterostructure. It is believed that the low-cost metal Ni is an alternative candidate for substituting the costly metals (Au, Ag and Pt) to improve the photocatalytic ability of semiconductor-based photocatalysts.

A p-i-n junction diode based on locally doped carbon nanotube network.

A p-i-n junction diode constructed by the locally doped network of single-walled carbon nanotubes (SWNTs) was investigated. In this diode, the two opposite ends of the SWNT-network channel were selectively doped by triethyloxonium hexachloroantimonate (OA) and polyethylenimine (PEI) to obtain the air-stable p- and n-type SWNTs respectively while the central area of the SWNT-network remained intrinsic state, resulting in the formation of a p-i-n junction with a strong built-in electronic field in the SWNTs. The results showed that the forward current and the rectification ratio of the diode increased as the doping degree increased. The forward current of the device could also be increased by decreasing the channel length. A high-performance p-i-n junction diode with a high rectification ratio (~10(4)), large forward current (~12.2 µA) and low reverse saturated current (~1.8 nA) was achieved with the OA and PEI doping time of 5 h and 18 h for a channel length of ~6 µm.

The microwave-assisted solvothermal synthesis of a crystalline two-dimensional covalent organic framework with high CO2 capacity.

We report the synthesis of a two-dimensional enamine-linked covalent organic framework (COF) using a rapid microwave-assisted solvothermal method in significantly less time and high yield under a relatively low temperature. This COF was found to have a high crystallinity, high stability, high BET surface area, and a high CO2 capacity and adsorption selectivity of CO2/N2.

Progress of electrospun fibers as nerve conduits for neural tissue repair.

Nerve tissue regeneration approaches have gained much attention in recent years, and nerve conduits (NCs), which facilitate nerve tissue regeneration, have become an attractive alternative to nerve autologous graft. Several methods are proposed to fabricate NCs, including electrospinning, which is a widely used approach for NCs and other tissue scaffolds, and has advantages such as the ability to control the thickness, diameter and porosity of fibers, as well as its simple experimental set up. This article gives an overview of electrospun fibers for nerve conduits utilized in peripheral and central nerve regeneration. Natural and synthetic materials with different mechanical strength, degradation rates and biocompatibility are proposed. Several bioactive proteins that can help the process of nerve regeneration are introduced. Finally, some approaches to control the morphology of electrospun fibers and to deliver bioactive proteins are discussed in detail.