Redox-based resistive switching memories (ReRAMs) are strongest candidates for the next-generation nonvolatile memories fulfilling the criteria for fast, energy efficient, and scalable green IT. These types of devices can also be used for selector elements, alternative logic circuits and computing, and memristive and neuromorphic operations. ReRAMs are composed of metal/solid electrolyte/metal junctions in which the solid electrolyte is typically a metal oxide or multilayer oxides structures. Here, this study offers an effective and cheap electrochemical approach to fabricate Ta/Ta O -based devices by anodizing. This method allows to grow high-quality and dense oxide thin films onto a metallic substrates with precise control over morphology and thickness. Electrochemical-oxide-based devices demonstrate superior properties, i.e., endurance of at least 10 pulse cycles and/or 10 I-V sweeps maintaining a good memory window with a low dispersion in R and R values, nanosecond fast switching, and data retention of at least 10 s. Multilevel programing capability is presented with both I-V sweeps and pulse measurements. Thus, it is shown that anodizing has a great prospective as a method for preparation of dense oxide films for resistive switching memories.
A generalization of the modeling equation of optical band gap values for ternary oxides, as a function of cationic ratio composition, is carried out based on the semiempirical correlation between the differences in the electronegativity of oxygen and the average cationic electronegativity proposed some years ago. In this work, a novel approach is suggested to account for the differences in the band gap values of the different polymorphs of binary oxides as well as for ternary oxides existing in different crystalline structures. A preliminary test on the validity of the proposed modeling equations has been carried out by using the numerous experimental data pertaining to alumina and gallia polymorphs as well as the crystalline ternary Ga(1–x)Al x O3 polymorphs (α-Ga(1–x)Al x O3 and β-Ga(1–x)Al x O3) covering a large range of optical band gap values (4.50–8.50 eV). To make a more rigorous test of the modeling equation, we extended our investigation to amorphous ternary oxides anodically formed on Al-d-metal alloys (Al-Nb, Al-Ta, and Al-W) covering a large range of d-metal composition (x d‑metal ≥ 0.2). In the last case, the novel approach allows one to overcome some difficulties experienced in fitting the optical band gap dependence from the Al-d-metal mixed anodic oxide composition as well as to provide a rationale for the departure, at the lowest d-metal content (x d‑metal < 0.2), from the behavior observed for anodic films containing higher d-metal content.
A critical assessment of the Photocurrent Spectroscopy (PCS) Technique for the semi-quantitative characterization of passive film and corrosion layers composition is carried out. We take into account more than three decades of PCS usage as "in-situ" analytical technique and related results as well as the criticism of the underlying semi-empirical correlation relating the measured optical bandgap (E g ) to the passive film composition. The discrepancies between the experimental data, gathered by PCS measurements, and E g estimates originating from recently developed Density Functional Theory based modeling of solid state properties are stressed with particular emphasis on the case of anodic passive film grown on technologically important alloys (Fe-Cr and stainless steels). The extension of this correlation to mixed oxides and its use for relating the oxide composition to the bandgap values is critically reviewed by comparing the predicted E g of mixed oxides with the experimental values. Suggestions on how to account for different bandgap values of oxide polymorphs and how to correlate the E g values to the composition of mixed s,p-d-metal oxides are presented and discussed on the basis of experimental results reported in the literature. On the basis of this assessment, the ability of PCS in providing quantitative information on the composition of passive film and corrosion layer is generally confirmed. Fujimoto (fujimoto@mat.eng.osaka-u.ac.jp) and HeeJin Jang (heejin@chosun.ac.kr). . This paper is a Critical Review in Electrochemical and Solid State Science and Technology (CRES 3 T). This article was reviewed by ShinjiPhotocurrent Spectroscopy (PCS) is currently employed for the characterization of solid-state properties of semiconducting and insulating materials, since the knowledge of their bandgap is a prerequisite to any possible application in different fields such as solar energy conversion (photoelectrochemical and photovoltaic solar cells, photocatalysis) and microelectronics (high-k, high band-gap materials). 1,2In the last 20-30 years an increasing number of electrochemists working in the field of corrosion have been attracted by this technique owing to its versatility and ability to scrutinize "in-situ" corrosion layers and passive films having semiconducting or insulating behavior. In previous as well as in very recent works 3-7 we have shown that PCS is able to provide detailed information on characteristic energy levels of passive film/electrolyte junctions (flatband potential: U FB ; internal photoemission threshold: E th ; bandgap value: E g ). Such information is necessary for a deeper understanding of the possible mechanisms of charge transfer (electrons and ions) at the metal/corrosion layer/electrolyte interface. Further advantages stem from the fact that the PCS technique does not require particular surface finishing control, it can be used both on large areas as well as in microscopic regions of the electrode, and can reach high sensitivity by using a lock-in amplifier coupled to a mec...
Coatings were grown on the AZ31 Mg alloy by a hard anodizing process in the hot glycerol phosphate-containing electrolyte. Anodizing conditions were optimized, maximizing corrosion resistance estimated by impedance measurements carried out in Hank’s solution at 37 °C. A post anodizing annealing treatment (350 °C for 24 h) allowed us to further enhance the corrosion resistance of the coatings mainly containing magnesium phosphate according to energy-dispersive X-ray spectroscopy and Raman analyses. Gravimetric measurements revealed a hydrogen evolution rate within the limits acceptable for application of AZ31 in biomedical devices. In vitro tests demonstrated that the coatings are biocompatible with a preosteoblast cell line.
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