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Micropatterns of gold (Au) nanoarrays on inorganic and polymeric substrates were fabricated by combining block copolymer micelle nanolithography to obtain gold nanoarrays on glass, photolithography plus hydrofluoric acid (HF) etching to generate microislands, and transfer lithography to shift the gold micro/nanopatterns from glass to a bioinert poly(ethylene glycol) (PEG) hydrogel surface. Further the modification of the gold nanodots via cell-adhesive arginine-glycine-aspartate (RGD) ligands was carried out to achieve peptide micro/nanopatterns. Whereas the micro/nanopatterns of noble metals could be useful in various applications, the peptide micro/nanopatterns especially enable persistent cell localization on adhesive micropatterns of RGD nanoarrays on the background of potently nonfouling PEG hydrogels, and thus offer a powerful tool to investigate cell-material interactions on both molecular and cellular levels. As a demonstration, we cultured human mesenchymal stem cells (hMSCs) on micro/nanopatterns with RGD nanoarrays of nanospacings 46 and 95 nm, and with micropans of side lengths 35 and 65 μm (four groups in total). The osteogenic and adipogenic differentiation of hMSCs was conducted, and the potential effect of RGD nanospacing and the effect of cell spreading size on cell differentiation were decoupled for the first time. The results reveal that RGD nanospacing, independent of cell spreading size, acts as a strong regulator of cell tension and stem cell differentiation, which cannot be concluded unambiguously based on either merely micropatterns or nanopatterns.

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We report the mild hydrothermal synthesis of single-crystalline rutile TiO2 nanorod arrays (NRAs). The method reported here shows great versatility and can be used to grow TiO2 NRAs on a large diversity of substrates including Si, Si/SiO2, sapphire, Si pillars, and fluorine doped tin oxide (FTO)-covered glass. The average diameter and length of the nanorods prepared at typical conditions are ∼60 nm and 400 nm, respectively. Dye-sensitized solar cells assembled with the TiO2 NRAs grown on the FTO-covered glass as photoanode were prepared with a photoconversion efficiency of ∼1.10%.

Poly(ethylene terephthalate)/expanded graphite conductive composites were prepared by the melt-blending method. The relationships between the preparation methods, microstructures, and conductivity properties of the composites were studied with scanning electron microscopy and conductivity measurements. The results showed that the composites presented a low percolation threshold and strong anisotropic conductivity. The epoxy resin had a strong intercalation effect on the expanded graphite that led to the easy formation of the conductive network. With classical statistical percolation theory, the conductivity behaviors of the composites were investigated. The results indicated that the nonuniversal critical exponent should be attributed to the anisotropy of conductivity, the tunneling conduction, and the particular structure. In addition, preliminary studies on the crystallization and dynamic mechanical behavior of the composites were performed.