Defect engineering of BCZT-based piezoelectric ceramics with high piezoelectric properties

The intrinsic conduction mechanism and optimal sintering atmosphere of (Ba0.85Ca0.15)(Zr0.1Ti0.9)O3 (BCZT) ceramics were regulated by Mn-doping element in this work. By Hall and impedance analysis, the undoped BCZT ceramics exhibit a typical n-type conduction mechanism, and the electron concentration decreases with the increasing oxygen partial pressure. Therefore, the undoped ceramics exhibit best electrical properties (piezoelectrical constant d33 = 585 pC·N−1, electro-mechanical coupling factor kp = 56%) in O2. A handful of Mn-doping element would transfer the conduction mechanism from n-type into p-type. And the hole concentration reduces with the decreasing oxygen partial pressure for Mn-doped BCZT ceramics. Therefore, the Mn-doped ceramics sintered in N2 have the highest insulation resistance and best piezoelectric properties (d33 = 505 pC·N−1, kp = 50%). The experimental results demonstrate that the Mn-doping element can effectively adjust the intrinsic conduction mechanism and then predict the optimal atmosphere.

Effect of Doping Element and Electrolyte’s pH on the Properties of Hydroxyapatite Coatings Obtained by Pulsed Galvanostatic Technique

Hydroxyapatite (HAp) is the most widely used calcium phosphate as a coating on metal implants due to its biocompatibility and bioactivity. The aim of this research is to evaluate the effect of the pH’s electrolyte and doping element on the morphology, roughness, chemical, and phasic composition of hydroxyapatite-based coatings obtained by pulsed galvanostatic electrochemical deposition. As doping elements, both Sr and Ag were selected due to their good osseoinductive character and antibacterial effect, respectively. The electrolytes were prepared at pH 4 and 5, in which specific concentrations of Sr, Ag, and Sr + Ag were added. In terms of morphology, all coatings consist in ribbon-like crystals, which at pH 5 appear to be a little larger. Addition of Sr did not affect the morphology of HAp, while Ag addition has led to the formation of flower-like crystals agglomeration. When both doping elements were added, the flowers like agglomerations caused by the Ag have diminished, indicating the competition between Sr and Ag. X-Ray Diffraction analysis has highlighted that Sr and/or Ag have successfully substituted the Ca in the HAp structure. Moreover, at higher pH, the crystallinity of all HAp coatings was enhanced. Thus, it can be said that the electrolyte’s pH enhances to some extent the properties of HAp-based coatings, while the addition of Sr and/or Ag does not negatively impact the obtained features of HAp, indicating that by using pulsed galvanostatic electrochemical deposition, materials with tunable features dictated by the function of the coated medical device can be designed.

Influence of Different Solutions on Corrosion Materials Based on Fe-Mg

This work deals with a current topic, which are biodegradable sintered Fe-based materials and their corrosion. These materials may be suitable for applications where gradual decomposition is required. An important parameter is not only the mechanical properties so that the material can withstand the load, but above all the corrosion properties and the degradation process. In this work, sintered materials based on Fe-Mg are tested. The introductory part is an introduction to the corrosion processes of the basic components of the tested systems, i.e. Fe. The practical part is focused on the preparation of samples based on Fe with the doping element Mg.

SYNTHESIS OF GRAPHENE-LIKE STRUCTURES BY A PLASMA-ARC DISCHARGE IN LIQUID NITROGEN

Using scanning electron microscopy, X-ray photoelectron spectroscopy, and Raman scattering we studied the charge state of matrix and doping element atoms on the surface, morphology, and defects in the structure of graphene-like materials synthesized by plasma-arc discharge in liquid nitrogen.

Durability of Alternative Metal Oxide Supports for Application at a Proton-Exchange Membrane Fuel Cell Cathode—Comparison of Antimony- and Niobium-Doped Tin Oxide

In this study, the resistance to corrosion of niobium-doped tin dioxide (Nb-doped SnO2, NTO) and antimony-doped tin oxide (Sb-doped SnO2, ATO) supports has been probed for proton-exchange membrane fuel cell (PEMFC) application. To achieve this goal, ATO or NTO supports with loose-tube (fiber-in-tube) morphology were synthesized using electrospinning and decorated with platinum (Pt) nanoparticles. These cathode catalysts were submitted to two different electrochemical tests, an accelerated stress test following the EU Harmonised Test Protocols for PEMFC in a single cell configuration and an 850 h test in real air-breathing PEMFC systems. In both cases, the dissolution of the doping element was measured either by inductively coupled plasma mass spectrometry (ICP–MS) performed on the exhaust water or by energy dispersive X-ray spectrometry (X-EDS) analysis on ultramicrotomed membrane electrode assembly (MEA), and correlated to the performance losses upon ageing. It appears that the NTO-based support leads to lower performances than the ATO-based one, mainly owing to the low electronic conductivity of NTO. However, in the case of ATO, dissolution of the Sb doping element is non-negligible and represents a major issue from a stability point-of-view.

Possibility of controlling the conduction mechanism by choosing a specific doping element in a praseodymium manganite system

Electrical properties of Pr0.7Ca0.3Mn0.9X0.1O3 (X = Co, Ni, Cr and Fe) systems have been investigated using impedance spectroscopy measurements.

ODS EUROFER Steel Strengthened by Y-(Ce, Hf, La, Sc, and Zr) Complex Oxides

Oxide dispersion-strengthened (ODS) materials contain homogeneous dispersions of temperature-stable nano-oxides serving as obstacles for dislocations and further pinning of grain boundaries. The strategy for dispersion strengthening based on complex oxides (Y-Hf, -Zr, -Ce, -La) was developed in order to refine oxide dispersion to enhance the dispersion strengthening effect. In this work, the strengthening of EUROFER steel by complex oxides based on Y and elements of the IIIB group (lanthanum, scandium) and IVB group (cerium, hafnium, zirconium) was explored. Interparticle spacing as a dispersoid characteristic appeared to be an important factor in controlling the dispersion strengthening contribution to the yield strength of ODS EUROFER steels. The dispersoid size and average grain size of ODS EUROFER steel were altered in the ranges of 5–13 nm and 0.6–1.7 µm, respectively. Using this strategy, the yield strength of the prepared alloys varied between 550 MPa and 950 MPa depending on the doping element.