Manipulating a quantum state via electrostatic gating has been of great importance for many model systems in nanoelectronics. Until now, however, controlling the electron spins or, more specifically, the magnetism of a system by electric-field tuning has proven challenging. Recently, atomically thin magnetic semiconductors have attracted significant attention due to their emerging new physical phenomena. However, many issues are yet to be resolved to convincingly demonstrate gate-controllable magnetism in these two-dimensional materials. Here, we show that, via electrostatic gating, a strong field effect can be observed in devices based on few-layered ferromagnetic semiconducting CrGeTe. At different gate doping, micro-area Kerr measurements in the studied devices demonstrate bipolar tunable magnetization loops below the Curie temperature, which is tentatively attributed to the moment rebalance in the spin-polarized band structure. Our findings of electric-field-controlled magnetism in van der Waals magnets show possibilities for potential applications in new-generation magnetic memory storage, sensors and spintronics.

Room temperature ferromagnetism (RTF) is observed in pure copper oxide (CuO) nanoparticles which were prepared by precipitation method with the postannealing in air without any ferromagnetic dopant. X-ray photoelectron spectroscopy (XPS) result indicates that the mixture valence states of Cu 1? and Cu 2? ions exist at the surface of the particles. Vacuum annealing enhances the ferromagnetism (FM) of CuO nanoparticles, while oxygen atmosphere annealing reduces it. The origin of FM is suggested to the oxygen vacancies at the surface/or interface of the particles. Such a ferromagnet without the presence of any transition metal could be a very good option for a class of spintronics.

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.

A growing amount of evidence supports that microRNA (miRNA) dysregulation is involved in cancer progression by directly downregulating multiple targets. Elucidating the underlying mechanism of miRNA in carcinogenesis may improve diagnostic and therapeutic strategies for malignancy. In the current study, we found that miR-105 expression was markedly downregulated in both hepatocellular carcinoma (HCC) cell lines and clinical HCC tissues, compared with normal human hepatocyte and adjacent non-cancerous tissues, respectively. Ectopic miR-105 expression suppressed, whereas inhibiting miR-105 promoted the proliferation and tumorigenicity of HCC cells both in vitro and in vivo. Furthermore, we demonstrated that miR-105 could deactivated the phosphoinositide 3-kinase (PI3K)/AKT signaling pathway by downregulating insulin receptor substrate-1, 3-phosphoinositide-dependent protein kinase-1 and AKT1 directly, resulting in increasing cyclin-dependent kinase inhibitors 1A and 1B (p21(Cip1) and p27(Kip1)) and decreasing cyclin D1 expression in HCC. Therefore, our results suggest that miR-105 functions as a potential tumor suppressor by inhibiting the PI3K/AKT signaling pathway and might represent a potential therapeutic target for HCC patients.

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.