Polarity-dependent reversible resistance switching in Ge–Sb–Te phase-change thin films

In this paper, we demonstrate reversible resistance switching in a capacitorlike cell using a Ge–Sb–Te film that does not rely on amorphous-crystalline phase change. The polarity of the applied electric field switches the cell resistance between lower- and higher-resistance states, as was observed in current-voltage characteristics. Moreover, voltage pulses less than 1.25 V showed this switching within time scales of microseconds with more than 40% contrast between the resistance states. The latter are found to be nonvolatile for months. The switching could also be achieved at nanoscales with atomic force microscopy with a better resistance contrast of three orders of magnitude.

Wear and friction performance of PTFE filled epoxy composites with a high concentration of SiO2 particles

In this work, the tribological performance of PTFE filled SiO2 particles–epoxy composites is investigated. Under a load of 60 N (~140 MPa contact pressure), the optimum content of PTFE lies between 10 and 15 wt%, which yields an ultralow coefficient of friction (CoF) in conjunction with a low wear rate of the composite when dry sliding against bearing steel balls within 1000 m. With 12.5 wt% PTFE in the composite, a CoF around 0.095 and a wear rate as low as 8.4×10−7 mm3/Nm were measured up to a sliding distance of around 2000 m. After 2000 m, eventually the gradual accumulation of the fractured SiO2 particles and back-transferred steel on the worn composite surface leads to a significant increase of CoF. In the steady-state of sliding, smearing of the PTFE particles along the worn surface was observed together with fracturing of the SiO2 particles and cracking of the epoxy matrix. Successive EDS mapping shows the formation and evolution of a PTFE-containing third-body tribolayer on the worn surface of the composite. The thickness of the tribolayer was measured about 20–30 nm on the surface of SiO2 particles after sliding for more than 700 m

Local delamination on heavily deformed polymer-metal interfaces:evidence from microscopy

In this work the microstructure of interfaces present in heavily bi-axially deformed polymer-coated metal is studied. Cross sections of deformed polymer-coated steel are prepared using several polishing strategies, including the use of focused ion beam, and are imaged using optical microscopy and scanning electron microscopy. We find that the interfaces show significant details right down to the smallest scale observable with the preparation techniques used of about similar to 10 nm. Local delamination events at these deformed interfaces are observed and are found to be preferentially associated with overhanging parts on the interface. Overhanging parts are frequently observed, but only below a certain length-scale on the interfaces that are otherwise found to be self-affine up to a certain correlation length. The smallest detail includes the tail of the size distribution of the overhanging features. Together this suggests that the physical mechanisms determining the formation of critical features for adhesion operate at sub-grain level as well as at grain level

Atomic force microscopy imaging of transition metal layered compounds:A two‐dimensional stick–slip system

Various layered transition metal dichalcogenides were scanned with an optical-lever atomic force microscope (AFM). The microscopic images indicate the occurrence of strong lateral stick-slip effects. In this letter, two models are presented to describe the observations due to stick-slip, i.e., either as a static or as a dynamic phenomenon. Although both models describe correctly the observed shapes of the unit cell, details in the observed and simulated images point at dynamic nonequilibrium effects. This exact shape of the unit cell depends on cantilever stiffness, scan direction, and detector direction. (C) 1995 American Institute of Physics

Tunable self-organization of nanocomposite multilayers

In this letter we report the controlled growth and microstructural evolution of self-assembled nanocomposite multilayers that are induced by surface ion-impingement. The nanoscale structures together with chemical composition, especially at the growing front, have been investigated with high-resolution transmission electron microscopy. Concurrent ion impingement of growing films produces an amorphous capping layer 3 nm in thickness where spatially modulated phase separation is initiated. It is shown that the modulation of multilayers as controlled by the self-organization of nanocrystallites below the capping layer, can be tuned through the entire film.

Hard-yet-tough high-vanadium hierarchical composite coating:Microstructure and mechanical properties

In this work, we report a high-vanadium hierarchical coating prepared on the surface of nodular cast iron substrate by a low-cost plasma transferred arc (PTA) surface alloying process. The coating consists of a graded layer with an alloyed zone (AZ) rich in submicron sized granular (V-Ti-Nb-Cr-Mo) composite carbides on top of intermediate melted zone characterized by refined ledeburite and martensite. The dense spherical particles in the AZ are FCC structured MC-type (M = V, Ti and Nb) carbides which tend to aggregate while M7C3 and M2C carbides nucleate on MC. The super-lattice V8C7 maintains its cube-on-cube orientation relationship with TiC. The hardness of the AZ is 9.6 +/- 1.0 GPa, similar to 4 times that of the substrate. Nano- and micro-indentations point at a superior strength-toughness in the AZ, where cracks are deflected and bridged by the spherical MC carbides in a compressive residue stress state. The fracture mode appears to be rather ductile in the AZ whereas brittle failure appears in both the melted zone and substrate. TEM and EDS results confirm that such a micro architecture design, assisted by the rapid solidification rate of the PTA process, concurrently activates various strengthening micromechanisms including the precipitation hardening and grain refinement

Nano-galvanic coupling for enhanced Ag+ release in ZrCN-Ag films: antibacterial application

The antibacterial properties of materials developed for medical devices with embedded silver nanoparticles are enhanced by controlling the release of silver ions. In this study, a simple experimental procedure for the augmentation of the silver ion release from ZrCN-Ag coatings is described. The silver nanoparticles are embedded in an amorphous carbon matrix within the ZrCN coatings, to create nano-galvanic couples between the silver and the carbon phases. The galvanic couple promotes the oxidation of silver, and consequently, increases the silver release. It is demonstrated that coatings with a lower silver content, but integrating amorphous carbon phases, can release similar or even a larger amount of Ag+ ions than those with higher Ag content having just ZrCN and Ag phases. The antibacterial tests demonstrate that coatings with silver nanoparticles encapsulated into amorphous phase reveal a larger bacterial zone of inhibition compared to samples with similar or lower silver content. However, it is shown that the antibacterial effect of the coatings not only depends on the ability for silver ion release, but also on the availability of silver nanoparticles on the surface.This research is partially sponsored by FEDER funds through the program COMPETE - Programa Operacional Factores de Competitividade and by Portuguese national funds through FCT-Fundacao para a Ciencia e a Tecnologia, under the projects ANTIMICROBCOAT - PTDC/CTM/102853/2008 and in the framework of the Strategic Projects PEST-C/ FIS/UI607/2011", UID/EMS/00285/2013 and SFRH/BD/80947/2011