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Electrical mobility demands an increase of battery energy density beyond current lithium-ion technology. A crucial bottleneck is the development of safe and reversible lithium-metal anodes, which is challenged by short circuits caused by lithium-metal dendrites and a short cycle life owing to the reactivity with electrolytes. The evolution of the lithium-metal-film morphology is relatively poorly understood because it is difficult to monitor lithium, in particular during battery operation. Here we employ operando neutron depth profiling as a noninvasive and versatile technique, complementary to microscopic techniques, providing the spatial distribution/density of lithium during plating and stripping. The evolution of the lithium-metal-density-profile is shown to depend on the current density, electrolyte composition and cycling history, and allows monitoring the amount and distribution of inactive lithium over cycling. A small amount of reversible lithium uptake in the copper current collector during plating and stripping is revealed, providing insights towards improved lithium-metal anodes.

Vanadium dioxide (VO(2)) is a well-known semiconductor material with a band gap of 0.7 eV, and is seldom used as a photocatalyst. We report here a new crystal structure for nanostructured VO(2), with body-centered-cubic (bcc) structure and a large optical band gap of approximately 2.7 eV, which surprisingly shows excellent photocatalytic activity in hydrogen production. The bcc VO(2) phase exhibited a high quantum efficiency of approximately 38.7% when synthesized as nanorods. Using films of the aligned VO(2) nanorods, the hydrogen production rate can be tuned by varying the incident angle of UV light on the films and reaches a high rate of 800 mmol/m(2)/h from a mixture of water and ethanol under UV light, at a power density of approximately 27 mW/cm(2), allowing possible commercial application of this material as photoassisted hydrogen generators.

Arrays of vertically aligned, single crystalline silver nanorods were deposited on silicon substrates via the glancing angle deposition technique using an e-beam system. The single crystalline Ag nanorods are several tens of nanometres in diameter and several hundred nanometres in length and could serve as excellent surface-enhanced Raman scattering substrates. Using these nanorods, Rhodamine 6G molecules can be detected to a concentration limit of 10−14 mol L−1, showing the possibility of applications in the trace amount detection of organics.

In this research, ZnO nanowires doped with Mn2+ and Co2+ ions were synthesized through a facile and inexpensive hydrothermal approach, in which Mn2+ and Co2+ ions successfully substituted Zn2+ in the ZnO crystal lattice without changing the morphology and crystalline structure of ZnO. The atomic percentages of Mn and Co were 6.29% and 1.68%, respectively, in the doped ZnO nanowires. The photocatalytic results showed that Mn-doped and Co-doped ZnO nanowires both exhibited higher photocatalytic activities than undoped ZnO nanowires. Among the doped ZnO nanowires, Co-doped ZnO, which owns a twice active visible-light photocatalytic performance compared to pure ZnO, is considered a more efficient photocatalyst material. The enhancement of its photocatalytic performance originates from the doped metal ions, which enhance the light absorption ability and inhibit the recombination of photo-generated electron-hole pairs as well. The effect of the doped ion types on the morphology, crystal lattice and other properties of ZnO was also investigated.

ZnO films became ferromagnetic when defects were introduced by thermal-annealing in flowing argon. This ferromagnetism, as shown by the photoluminescence measurement and positron annihilation analysis, was induced by the singly occupied oxygen vacancy with a saturated magnetization dependent positively on the amount of this vacancy. This study clarified the origin of the ferromagnetism of un-doped ZnO thin films and provides possibly an alternative way to prepare ferromagnetic ZnO films.

When heated in a rapid thermal processor at 350 °C in air, cobalt thin (50 nm thick) films were transformed into Co(3)O(4) nanorods in minutes. The nanorods are single-crystalline and are typically several hundred nanometers long and several tens of nanometers in diameter. They exhibited room-temperature photoluminescence in the visible range and good field emission properties, i.e. a low turn-on field of ∼2.8 V µm(-1) and good stability at high emission currents. This study provides a simple but rapid approach that is compatible with microtechnology and is capable of fabricating metal oxide nanorods at low substrate temperatures, on a large scale.

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