Cuprous oxide films were successfully electrodeposited onto three different substrates through the reduction of copper lactate in alkaline solution at pH = 10. The substrates include indium tin oxide film coated glass, n-Si wafer with (001) orientation and Au film evaporated onto Si substrate. The substrate effects on the structural and optical properties of the electrodeposited films are investigated by in situ voltammetry, current versus time transient measurement, ex situ x-ray diffraction, scanning electron microscopy, UV-vis transmittance and reflectance and photoluminescence techniques. The results indicate that the choice of substrate can strongly affect the film morphology, structure and optical properties.

Nitrogen doped ZnO films are directly fabricated by the thermal oxidation of Zn3N2 films. Zn3N2 films are prepared by plasma-assisted metal-organic chemical vapour deposition (PA-MOCVD). By comparing with undoped ZnO photoluminescence spectra, a much stronger bound exciton emission due to a neutral nitrogen acceptor (A0X) is observed at low temperature. The neutral acceptor level is located at 130 meV above the valence band maximum. To demonstrate the quality of ZnO:N thin films as a p-type, a Zn3N2/n-Si heterojunction structure was first fabricated. With an increase of oxidation temperature, the structure has gradually shown p–n junction rectification characteristics from I–V measurements.

Myxobolus wulii (=Myxosoma magna) was first described from the gills of goldfish, Carassius auratus auratus, in China. Subsequently, a myxosporean infecting the hepatopancreas of allogynogenetic gibel carp, C. auratus gibelio, was designated as a different species, Myxobolus guanqiaoensis, although the morphological features were almost identical to those of M. wulii. In Japan, an unidentified Myxobolus sp. was found in the gills and hepatopancreas of goldfish. Morphological and molecular analyses in the present study identified these myxosporeans as M. wulii, which was thus shown to use different habitats in the host fish. Phylogenetic analyses of small subunit ribosomal RNA gene sequences showed that M. wulii is closely related to two gillinfecting Myxobolus species, M. ampullicapsulatus and M. longisporus. Fish infected with M. wulii in the hepatopancreas exhibit swollen abdomens and chronic mortality. Hepatopancreas tissues are virtually destroyed and replaced with plasmodia of M. wulii. A remarkable difference in susceptibility to M. wulii between two clones of allogynogenetic gibel carp was observed, suggesting that resistance to the myxosporean infection was established in a clone of fish bred by allogynogenesis.