Jing Lin

Light triggered interfacial damage self-healing of poly(p-phenylene benzobisoxazole) fiber composites

The interfacial microcracks in the resin matrix composites are difficult to be detected and repaired. However, the self-healing concept provides opportunities to fabricate composites with unusual properties. In the present study, photothermal conversion Ag-Cu2S nanoparticles were immobilized onto poly(p-phenylene benzobisoxazole) (PBO) fibers via a polydopamine chemistry. Benefitting from the photothermal effects of Ag-Cu2S, the obtained PBO fibers (Ag-Cu2S-PBO) efficiently converted the light energy into heat under Xenon lamp irradiation. Then, single PBO fiber composites were prepared using thermoplastic polyurethane as the matrix. It was found that the interfacial damage caused by single fiber pull-out was simply self-healed by Xe light irradiation. This wonderful interfacial damage self-healing property was mainly attributed to the in situ heating generation via photothermal effects of Ag-Cu2S in the composite interface. This paper reports a novel strategy to construct advanced composites with light-triggered self-healing properties, which will provide inspiration for preparing high performance composite materials.

Durably Antibacterial and Bacterially Antiadhesive Cotton Fabrics Coated by Cationic Fluorinated Polymers

Considerable attention has been devoted to producing antibacterial fabrics due to their very wide applications in medicine, hygiene, hospital, etc. However, the poor antibacterial durability and bad bacterial antiadhesion capacity of most existing antibacterial fabrics limit their applications. In this work, a series of antibacterial and polymeric quaternary ammonium monomers with different alkyl chain length were successfully synthesized to copolymerize with fluorine-containing and other acrylic monomers to generate cationic fluorinated polymer emulsions and durably antibacterial and bacterially antiadhesive cotton fabrics. The relation between antibacterial constituent and its antibacterial activity was investigated. The study indicated that the alkyl chain length and contents of the antibacterial monomers, as well as the add-on percentage of polymer greatly influenced the antibacterial activities of the fabrics. In addition, it was found that incorporation of fluorine component into the polymer greatly enhanced the antibacterial activity and bacterial antiadhesion of the treated fabrics due to the low surface energy induced hydrophobicity. Finally, antibacterial and antiadhesive models of action of the obtained fabrics were illustrated.

Carbon Nanomaterials in Direct Liquid Fuel Cells

Fuel cells have attracted more attentions due to many advantages they can provide, including high energy efficiency and low environmental burden. To form a stable, low cost and efficient catalyst, we presented here the state of the art of electrocatalyst fabrication approaches, involving carbon nanotubes and their multifunctional nanocomposites incorporated with noble metals, such as Pt, Pd, Au, their binary and ternary systems. Both fuel oxidation reactions and oxygen reduction reactions were emphasized with comprehensive examples and future prospects.

Bio-gel derived nickel/carbon nanocomposites with enhanced microwave absorption

A bio-gel derived strategy was used to construct Ni/C nanocomposites consisting of three-dimensional (3-D) carbon networks with embedded nickel nanoparticles. The amorphous carbon prevents agglomeration of the nickel nanoparticles and thus contributes to a good impedance match. The microwave absorption properties of the Ni/C nanocomposites were optimized according to percolation theory for good impedance matching. As a result, microwave absorbing coatings, which have the advantages of thin thickness (1.75 and 1.5 mm) and light weight (25 and 30 wt%), were achieved with excellent absorbing properties (90% microwave absorption) and a broad bandwidth (13.6–18 GHz and 13.2–18 GHz). The absorbing properties were mainly attributed to the dielectric relaxation processes at 2–18 GHz from the multilevel interface, porous carbon materials and nanoscale nickel nanoparticles in the Ni/C nanocomposites. It is believed that this work not only helps to elucidate the mechanism of absorption but also provides a new design paradigm for determining the optimal content of absorbers using percolation theory. The bio-gel derived strategy paves a possible way for the mass synthesis of microwave absorbers.

In-situ grown nickel selenide onto graphene nanohybrid electrodes for high energy density asymmetric supercapacitors

Nickel selenide (NiSe) nanoparticles uniformly supported on graphene nanosheets (G) to form NiSe-G nanohybrids were prepared by an in situ hydrothermal process. The uniform distribution of NiSe on graphene bestowed the NiSe-G nanohybrid with faster charge transport and diffusion along with abundant accessible electrochemical active sites. The synergistic effect between NiSe nanoparticles and graphene nanosheets for supercapacitor applications was systematically investigated for the first time. The freestanding NiSe-G nanohybrid electrode exhibited better electrochemical performance with a high specific capacitance of 1280 F g-1 at a current density of 1 A g-1 and a capacitance retention of 98% after 2500 cycles relative to that of NiSe nanoparticles. Furthermore, an asymmetric supercapacitor device assembled using the NiSe-G nanohybrid as the positive electrode, activated carbon as the negative electrode and an electrospun PVdF membrane containing 6 M KOH as both the separator and the electrolyte delivered a high energy density of 50.1 W h kg-1 and a power density of 816 W kg-1 at an extended operating voltage of 1.6 V. Thus, the NiSe-G nanohybrid can be used as a potential electrode material for high-performance supercapacitors.

Solvothermal synthesis, characterization and photocatalytic property of zirconium dioxide doped titanium dioxide spinous hollow microspheres with sunflower pollen as bio-templates

Zirconium dioxide (ZrO2) doped titanium dioxide (TiO2) spinous hollow microspheres were successfully prepared through a facile solvothermal method using sunflower pollen as bio-templates. The products were characterized by scanning electron microscopy (SEM), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), Fourier transform infrared spectroscopy (FT-IR), N2 adsorption-desorption isotherms and UV-Vis diffuse reflectance spectroscopy. It was found that the products have spinous microsphere morphology with an approximate diameter of 12u202fμm. The ZrO2 doped TiO2 hollow microspheres exhibited a higher photocatalytic activity in the degradation of Rhodamine B (RhB) in aqueous solutions under UV-light irradiation compared with TiO2 hollow microspheres and ZrO2-doped TiO2 particles. In particular, the removal of RhB followed pseudo-first-order kinetics, and 96.3% of RhB was degraded in 60u202fmin under UV-light irradiation when ZrO2 doped TiO2 spinous hollow microspheres were used as the photocatalysts. Neutral and alkaline conditions were found to favor over acidic conditions for the photocatalytic degradation of RhB. Furthermore, scavenging experiments indicated that photogenerated holes (h+) and radicals (OH and O-2) were the main reactive species in the photocatalytic process using ZrO2 doped TiO2 hollow microspheres as the catalysts under UV light irradiation.