The room-temperature ferromagnetism of Zn1−x Al x O nanoparticles synthesized by a sol−gel method is reported in this paper. X-ray diffraction and selected area electron diffraction results show that the Al atoms have successfully substituted for some of the Zn atoms in the ZnO lattice without forming other new phases. The results also show that the samples possess a typical wurtzite structure. Declaration of ferromagnetism at room temperature has been established with the observed hysteresis and the coercive field in hysteresis loops. Magnetic measurements indicate that the saturation magnetization of the samples is sensitive to the content of Al dopants and that, for Zn0.97Al0.03O, the saturation magnetization reaches the maximum of 0.012 emu/g. Combining with the results of Raman, photoluminescence, and X-ray photoelectron spectroscopies, it is suggested that the observed ferromagnetic ordering of the Zn1−x Al x O nanoparticles is related to the doping-induced oxygen vacancies.

Amorphous and crystalline Al2O3 nanoparticles were synthesized by a sol–gel method with postannealing at different temperatures. Magnetism measurements have indicated that all Al2O3 nanoparticles exhibit intrinsic room temperature ferromagnetism, and the saturation magnetism of the samples increases after vacuum annealing, whereas bulk Al2O3 presents paramagnetism. Electron spin resonance and fitting results of O 1s X-ray photoelectron spectroscopy reveal that the origin of the ferromagnetism in Al2O3 nanoparticles could be attributed to the singly charged oxygen vacancies (F+ centers). The variation of the relative area of oxygen vacancies and the number of free electrons is consistent with the change of saturation magnetization for the samples. Combined with these results, a direct correlation of ferromagnetism with F+ centers exchange mechanism is established.

Single-crystalline CoO nanospheres with the size distribution between 40 and 250 nm were prepared by a solvothermal method. Magnetic measurements indicate that the vacuum-annealed samples show room temperature ferromagnetism except for the CoO nanospheres of 250 nm, which still exhibit paramagnetism after being postannealed in vacuum atmosphere (10−3 Pa) at 250 °C as others. The saturation magnetization of all postannealed samples monotonically increases with the decrease of nanosphere diameter. No other impurity phases are observed for the postannealed samples, indicating that the revealed ferromagnetism is an intrinsic property. The fitted XPS results of O 1s spectra indicate that the variations of oxygen vacancies concentration are consistent with the variations of saturation magnetization for the vacuum-annealed samples, suggesting that the formed oxygen vacancies at the surface of the CoO nanospheres during the vacuum-annealing process account for the observed ferromagnetism.

Inorganic nanomaterials-based artificial enzymes (nanozymes) have received considerable attention over the past years. However, the substrates studied for nanozymes have so far been limited to small organic molecules. The catalytic oxidation of biomacromolecules, such as proteins, by nanozymes has not yet been reported to date. In this study, we report that cuprous oxide nanoparticles (CuO NPs) possess cytochrome c oxidase (CcO)-like activity and catalyze the oxidation of cytochrome c (Cyt c), converting it from the ferrous state to the ferric state under atmospheric oxygen conditions. Furthermore, the CcO-like activity of CuO NPs is pH- and size-dependent. The lower the solution pH and the smaller the particle size, the higher the CcO-like activity. The artificial Cyt c-CuO NPs system closely mimics the native Cyt c-CcO enzyme system, which opens new vistas in enzyme construction and potential applications.

Preferred oriented ZnFe2O4 nanowire arrays with an average diameter of 16 nm were fabricated by post-annealing of ZnFe2 nanowires within anodic aluminum oxide templates in atmosphere. Selected area electron diffraction and X-ray diffraction exhibit that the nanowires are in cubic spinel-type structure with a [110] preferred crystallite orientation. Magnetic measurement indicates that the as-prepared ZnFe2O4 nanowire arrays reveal uniaxial magnetic anisotropy, and the easy magnetization direction is parallel to the axis of nanowire. The optical properties show the ZnFe2O4 nanowire arrays give out 370–520 nm blue-violet light, and their UV absorption edge is around 700 nm. The estimated values of direct and indirect band gaps for the nanowires are 2.23 and 1.73 eV, respectively.