No abstract

Recently, the authors observed ubiquitous polymer chain ordering in polymer micro- and nanostructures patterned by thermal nanoimprint. These polymer materials exhibit chain ordering during melt processing, which indicates that the double nanoimprint technique has been successfully performed. In this work, the authors present the double nanoimprint technique at elevated temperature for reducing the patterning size of thermoplastic functional polymers without the need for excessive imprint pressure, which eventually results in the size decrease in pattern formation. This double nanoimprint technique is a further application of thermal nanoimprint, followed by anisotropy of material properties, such as the refractive index and optical absorption.

No abstract

Despite tremendous importance in catalysis, the design and improvement of the oxide- metal interface has been hampered by the limited understanding on the nature of interfacial sites, as well as the oxide-metal interaction (OMI). Through the construction of well-defined Cu₂O-Pt, Cu₂O-Ag, Cu₂O-Au interfaces, we found that Cu₂O Nanostructures (NSs) on Pt exhibit much lower thermal stability than on Ag and Au, although they show the same surface and edge structures, as identified by element-specific scanning tunneling microscopy (ES-STM) images. The activities of the Cu₂O-Pt and Cu₂O-Au interfaces for CO oxidation were further compared at the atomic scale and showed in general that the interface with Cu₂O NSs could annihilate the CO-poisoning problem suffered by Pt group metals and enhance the interaction with O₂, which is a limiting step for CO oxidation catalysis on group IB metals. While both interfaces could react with CO at room temperature, the OMI was found to determine the reactivity of supported Cu₂O NSs by 1) tuning the activity of interfacial oxygen atoms and 2) stabilizing oxygen vacancies or vice versa, the dissociated oxygen atoms at the interface. Our study provides new insight for OMI and for the development of Cu-based catalysts for low temperature oxidation reactions.