Growth of (0001) facet-dominated, free-standing, piezoelectric zinc oxide (ZnO) nanostructures is challenged by the divergence of the surface energy due to intrinsic polarization. By controlling growth kinetics, we show the success of growing nanobelt-based novel structures whose surfaces are dominated by the polarized ±(0001) facets. Owing to the positive and negative ionic charges on the zinc- and oxygen-terminated ±(0001) surfaces, respectively, a spontaneous polarization is induced across the nanobelt thickness. As a result, right-handed helical nanostructures and nanorings are formed by rolling up single-crystal nanobelts; this phenomenon is attributed to a consequence of minimizing the total energy contributed by spontaneous polarization and elasticity. The polar-surface-dominated ZnO nanobelts are likely to be an ideal system for understanding piezoelectricity and polarization-induced ferroelectricity at nanoscale; and they could have applications as one-dimensional nanoscale sensors, transducers, and resonators.
Abstract Gesundheit, Infrastruktur oder Umweltüberwachung sowie Vernetzungs‐ und Verteidigungstechnologien sind nur einige der potenziellen Anwendungsbereiche für Mikro‐/Nanosysteme (MNS). Dabei sollten die MNS unabhängig von einer externen Stromversorgung arbeiten, und ihre Energie aus der Umgebung beziehen, in der sie eingesetzt werden. Dieser Aufsatz beschäftigt sich mit verschiedenen Ansätzen zur Energiegewinnung, um der zukünftigen Nachfrage nach autarken MNS gerecht zu werden.
Abstract It is demonstrated that the redox reaction behaviors of Pd nanoparticles in HAuCl 4 solutions can be substantially modified by the introduction of hexadecyl trimethyl ammonium bromide (CTAB) agents through systematic liquid cell transmission electron microscopy (LCTEM) investigations. The gradual dissolution of Pd nanoparticles is observed when HAuCl 4 solution is pumped into liquid flow cells, the etching characteristics of which are depended on both HAuCl 4 concentrations and incident electron doses. In comparison, with the presence of CTAB agents, the dominated phenomenon appears to be the precipitation of Au species and incorporation onto the surface of Pd seeds. It is also observed that the rapid growth of Au on Pd seeds occurs by loading Pd and HAuCl 4 solutions into static liquid cells. The resultant Au shells exhibit rather sparse structural configurations and are formed possibly by homogeneous nucleation/coalescence of Au species as well as monomer attachments. The observed Au‐shell growth instead of Pd dissolution is attributed to the presence of the residual regents, which may be also responsible for the initially already existing small Au adsorptions at the corner/edge sites of Pd seeds. The study provides a useful reference for the convenient fabrication of complex nanostructures and functional nanomaterials in a controllable way.