ZnO films were prepared by pulsed laser deposition on a-plane sapphire substrates under N2 atmosphere. Ferromagnetic loops were obtained with the superconducting quantum interference device at room temperature, which indicate a Curie temperature much above room temperature. No clear ferromagnetism was observed in intentionally Cu-doped ZnO films. This excludes that Cu doping into ZnO plays a key role in tuning the ferromagnetism in ZnO. 8.8% negative magnetoresistance probed at 5K at 60kOe on ferromagnetic ZnO proves the lack of s-d exchange interaction. Anomalous Hall effect (AHE) was observed in ferromagnetic ZnO as well as in nonferromagnetic Cu-doped ZnO films, indicating that AHE does not uniquely prove ferromagnetism. The observed ferromagnetism in ZnO is attributed to intrinsic defects.
Memristive devices present a new device technology allowing for the realization of compact non-volatile memories. Some of them are already in the process of industrialization. Additionally, they exhibit complex multilevel and plastic behaviors, which make them good candidates for the implementation of artificial synapses in neuromorphic engineering. However, memristive effects rely on diverse physical mechanisms, and their plastic behaviors differ strongly from one technology to another. Here, we present measurements performed on different memristive devices and the opportunities that they provide. We show that they can be used to implement different learning rules whose properties emerge directly from device physics: real time or accelerated operation, deterministic or stochastic behavior, long term or short term plasticity. We then discuss how such devices might be integrated into a complete architecture. These results highlight that there is no unique way to exploit memristive devices in neuromorphic systems. Understanding and embracing device physics is the key for their optimal use.
In this paper we show that ferromagnetism can be induced in pure TiO2 single crystals by oxygen ion irradiation. By combining x-ray diffraction, Raman-scattering, and electron spin resonance spectroscopy, a defect complex, i.e. Ti 3+ ions on the substitutional sites accompanied by oxygen vacancies, has been identified in irradiated TiO2. This kind of defect complex results in a local (TiO6−x) stretching Raman mode. We elucidate that Ti 3+ ions with one unpaired 3d electron provide the local magnetic moments.Recently, ferromagnetism has been observed in nonmagnetically doped, but defective oxides, including TiO 2 1,2,3,4 . This kind of observation challenges the conventional understanding of ferromagnetism, which is rather due to spin-split states or bands. Thus, one fundamental question must be answered: where are the moments located? Intensive theoretical work has been performed to understand the ferromagnetism in defective oxides 5,6,7 . In these papers, the triplet states of p-like electrons, located at cation or oxygen vacancies, yield the local moments, leading to a kind of ferromagnetism without the involvement of 3d electrons. Experimentally the ferromagnetism in undoped TiO 2 has been found to relate with oxygen vacancies (O V ) 2,3 , however, its mechanism remains unclear. It is worth to note that Ti 3+ ions with one 3d electron are usually generated in slightly reduced TiO 2 . When O is removed, the excess electrons are unpaired 8 . They can occupy the nearby localized Ti 3d orbit and therefore convert Ti 4+ ions to Ti 3+ ions. In a reduced rutile TiO 2 (110) surface, such a defect complex, Ti 3+ -O V , has been well studied by first-principles calculations 9,10 and experimentally by resonant photoelectron diffraction 11 . Therefore, experimental work is needed to clarify whether the magnetic moments in defective TiO 2 is due to unpaired 3d electrons localized on Ti 3+ ions.Ion irradiation is a non-equilibrium and reproducible method of inducing defects. Energetic ions displace atoms from their equilibrium lattice sites, thus creating mainly vacancies and interstitials. The amount of defects can be controlled by the ion fluence and energy. In this paper, we irradiated rutile TiO 2 single crystals with 2-MeV O ions, resulting in a projected range of 1.52 µm and a longitudinal straggling of 0.16 µm as calculated by SRIM code (The Stopping and Range of Ions in Matter) 12 . As a result of this irradiation, the formation of Ti/O vacancies/interstitials is expected 12 . We selected high-energy oxygen ions as projectiles to avoid the introduction of foreign elements. Moreover, from a ballistic point of view, the creation of oxygen vacancies is more efficient, e.g., by a factor of 1.5 larger than the Ti-vacancy creation. From SRIM calculations it is also evident that, at the given energy, the maximum atomic concentration of the implanted oxygen ions is by a factor of 500 smaller than the concentration of oxygen recoils. For the region of maximum defect creation, i.e., at the end of the ion range, those project...
High-quality single crystals of ZnO in the as-grown and N + ion-implanted states have been investigated using a combination of three experimental techniques-namely, positron lifetime/slow positron implantation spectroscopy accompanied by theoretical calculations of the positron lifetime for selected defects, temperaturedependent Hall ͑TDH͒ measurements, and deep level transient spectroscopy ͑DLTS͒. The positron lifetime in bulk ZnO is measured to be ͑151± 2͒ ps and that for positrons trapped in defects ͑257± 2͒ ps. On the basis of theoretical calculations the latter is attributed to Zn+ O divacancies, existing in the sample in neutral charge state, and not to the Zn vacancy proposed in previous experimental work. Their concentration is estimated to be 3.7ϫ 10 17 cm −3 . From TDH measurements the existence of negatively charged intrinsic defects acting as compensating acceptors is concluded which are invisible to positrons-maybe interstitial oxygen. This view is supported from TDH results in combination with DLTS which revealed the creation of the defect E1, and an increase in concentration of the defect E3 after N + ion implantation, and peculiarities in the observation of the defect E4.
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