Novel Cr(3+) doped zinc gallogermanate (ZGGO) nanoparticles with 697 nm near-infrared (NIR) super long afterglow were prepared via a hydrothermal method. Subsequently, a vacuum-annealing strategy was adopted to improve NIR afterglow in ZGGO:Cr(3+) nanoparticles. For the sample annealed at 800 °C, no variation in the particle size is observed, the persistent luminescence increases by an order of magnitude (∼14 times) and the NIR afterglow time reaches more than 15 hours relative to the as-prepared sample. After annealing at temperatures higher than 880 °C, the persistent luminescence of the nanoparticles is enhanced, but they show aggregated-surface behavior. Meanwhile, shallow and deep traps are generated, related to the antisite defects and VGe-Cr(3+)-VO defect clusters, respectively. Finally, we apply ZGGO:Cr(3+) persistent luminescence nanoparticles (PLNPs) to a human serum albumin (HSA) colloid solution, and more than 1 h of NIR persistent luminescence is detected under 320 nm excitation. The quenching effect of NIR luminescence by OH(-) in the HSA solution is observed based on the reduced contribution of surface Cr(3+) in PLNPs to NIR luminescence. Our results suggest that ZGGO:Cr(3+) PLNPs have potential applications for in vivo bio-imaging.

(Mn, N)-codoped ZnO films were grown on fused silica substrates by reactive magnetron cosputtering. X-ray diffraction measurements reveal that the films have the single-phase wurtzite structure with c-axis preferred orientation. X-ray photoelectron spectroscopy studies indicate the incorporation of both divalent Mn2+ and trivalent N3− ions into ZnO lattice. Acceptor doping with nitrogen partly compensates the “native donors,” which results in a low electron concentration of 3.16×1016cm−3 though p-type conductivity is not achieved. (Mn, N)-codoped ZnO films show significant ferromagnetism with Curie temperature above 300K. The mechanism of ferromagnetic coupling in codoped ZnO is discussed based on a bound magnetic polaron model.

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The effects of zinc oxide nanoparticles (ZnO NPs) on the root growth, root apical meristem mitosis and mitotic aberrations of garlic (Allium sativum L.) were investigated. ZnO NPs caused a concentration-dependent inhibition of root length. When treated with 50 mg/L ZnO NPs for 24 h, the root growth of garlic was completely blocked. The 50% inhibitory concentration (IC(50)) was estimated to be 15 mg/L. The mitosis index was also decreased in a concentration- and time-dependent manner. ZnO NPs also induced several kinds of mitotic aberrations, mainly consisted of chromosome stickiness, bridges, breakages and laggings. The total percentage of abnormal cells increased with the increase of ZnO NPs concentration and the prolongation of treatment time. The investigation provided new information for the possible genotoxic effects of ZnO NPs on plants.