Parallel arrays of either Au or Pd nanowires were fabricated on glass substrates via the electrochemical process of lithographically patterned nanowire electrodeposition (LPNE) and then characterized with scanning electron microscopy (SEM) and a series of optical diffraction measurements at 633 nm. Nanowires with widths varying from 25 nm to 150 nm were electrodeposited onto nanoscale Ni surfaces created by the undercut etching of a photoresist pattern on a planar substrate. Using a simple transmission grating geometry, up to 60 diffraction orders were observed from the nanowire gratings, with separate oscillatory intensity patterns appearing in the even and odd diffraction orders. The presence of these intensity oscillations is attributed to LPNE array fabrication process, which creates arrays with alternating interwire spacings of distances d+Δ and d−Δ , where d = 25 μm and the asymmetry Δ varied from 0 to 3.5 μm. The amount of asymmetry could be controlled by varying the LPNE undercut etching time during the creation of the nanoscale Ni surfaces. The Fourier transform of a mathematical model of the nanowire array was used to predict the diffraction intensity patterns and quantitatively determine Δ for any grating. Additional sensitivity and an expanded diffraction order range were obtained through the use of external reflection (ER) and total internal reflection (TIR) diffraction geometries.
A very low dosage of graphene oxide (GO) can enhance the mechanical durability of cement composites, but the reinforcing enhancement is highly dependent on the uniform dispersion of graphene in the matrix. Carboxylic groups at GO nanosheets have a decisive effect on GO aggregation in an alkaline cement solution because they have a strong complexation ability with aqueous Ca2+ released by cement hydration and subsequently crosslinks the adjacent graphene sheets, causing the immediate coagulation of GO. The available methods of homogeneously dispersing GO in a cement slurry cannot completely eliminate this carboxylic-crosslinking-induced GO coagulation. In this study, many hydroxyl groups were introduced onto the edge and planar nanosheets to prepare water-soluble hydroxylated graphene (HO-G) by facile ball milling. The structure of HO-G was thoroughly characterized in detail, and its dispersion behavior in pure water and Ca(OH)2 was extensively investigated. These results showed that the prepared HO-G exhibited good hydrophilicity and excellent colloidal dispersion ability against high pH and Ca2+ ions compared to GO. The effect of HO-G on the workability, mechanical strength, and chloride penetrability of a cement mortar was further studied. At a content of 0.03% by cement mass, HO-G provided 28.62 and 21.19% enhancements of compressive strength and 3.85 and 7.89% enhancements of flexural strength at 3 and 28 days, respectively, while the non-steady-state migration coefficient decreased by 31.51% compared to the reference mortar. Compared to GO, a lower dosage of HO-G exhibited a similar reinforcing effect to cement composites with little adverse impact on the fluidity of the fresh cement slurry. Moreover, the addition of HO-G could refine the pore structure, accelerate the hydration process of cement to some degree, and generate more hydration products so that the structure of the cement mortar was densified. Considering its environmentally friendly preparation, HO-G, as a promising reinforcing nanofiller, could provide a new solution to develop nanoengineered cement composites.
The reduced graphene oxide (RGO) was added to polycarbonate (PC) through solvent mixing. The influences of RGO on the free volumes and electrical conductivity of PC were systemically studied by positron annihilation lifetime spectroscopy (PALS), Fouriertransform infrared spectroscopy, transmission electron microscope, and electrical conductivity measurements for PC/RGO nanocomposites. The nanosized effect, good conductivity of RGO, and strong interfacial interaction between RGO and PC result in the low conductive threshold of 0.36 wt %. Ten orders of magnitude increase in electrical conductivity was obtained. The results of PALS indicate the properties of free volumes fluctuate around the conductive percolation threshold. The conformational change of PC segments in the interfacial region induced by the strong interfacial interaction leads to an increase in free volume radius. The concentration of free volume decreases due to the depression of free volume holes as the introduction of RGO. Significantly, an exponential function is proposed to describe the effect of relative fractional free volume on the electrical conductivity, suggesting that free volume plays an important role in regulating electrical conductivity of PC/RGO. The physical quantity f d that refers required fractional free volume of polymer composites from insulating to conducting phase is found.
A confirned polymerization method was employed to fabricate self-standing PPy/GO film for all-solid-state supercapacitor.
Heterojunctioned ZnO/Bi2S3 nanocomposites were prepared via a facile solvothermal method. The obtained photocatalysts were characterized by X-ray powder diffraction (XRD), Scanning electron microscopy (SEM), High resolution transmission electron microscopy (HRTEM), X-ray photoelectron spectroscopy (XPS), UV-Vis diffuse reflectance spectroscopy (DRS), and Photoelectrochemical and Photoluminescence spectroscopy (PL), respectively. The results showed that ZnO/Bi2S3 composites exhibited the sandwiched-like structure, where ZnO nanoparticles were randomly embedded between Bi2S3 nanoflakes. The performance of photocatalytic Cr(VI) reduction under visible light indicated that ZnO/Bi2S3 composites exhibited high-efficiency photocatalytic activity in comparison with either Bi2S3 or ZnO. The 5%-ZnO/Bi2S3 photocatalyst removed 96% of Cr(VI) within 120 min at 20 mg/L initial concentration of Cr(VI). The enhanced performance of ZnO/Bi2S3 photocatalysts could be ascribed to the increased light harvesting and the effective separation and transfer of the photogenerated charge carriers across the heterojunction interface of the ZnO/Bi2S3 composite. This work could pave the way for the design of new hetero-structured materials and has great potential in environmental remediation.
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