Barium titanate materials displaying a positive temperature coefficient of resistivity are ubiquitously employed as thermistors in electrical current and voltage control systems, as well as in gas and thermal sensing applications. The positive temperature coefficient of resistivity effect is widely accepted to be a grain boundary-based phenomenon, although detailed studies on grain boundary structure and chemistry, and their influence on the resulting electrical properties, are seriously lacking. Tailoring of the positive temperature coefficient of resistivity electrical characteristics, for specific high-value applications, will require improved understanding and control over grain boundary phenomenon. A comprehensive overview of the development of barium titanate-based positive temperature coefficient of resistivity ceramics is initially presented. We then advance to a discussion on emerging grain boundary characterization techniques, specifically, a stereographic analysis of electron backscatter diffraction data that could assist in enhancing control over BaTiO₃ defect chemistry and microstructure, through characterization and subsequent manipulation of the population of grain boundary types. These techniques have great potential for increasing the understanding of the delicate interplay between processing conditions, chemistry, microstructure, and functional electrical properties, and are relevant to the development of advanced, high-performance ceramics and electroceramics in general. Contemporary advancements in the field, such as lead-free positive temperature coefficient of resistivity effect materials and multilayer miniaturized systems based on hypostoichiometric barium compositions, are reviewed. Finally, perspectives on future lines of thermistor research, with a focus on the energy sector, are presented including applications in gas separation and chemical sensing.

Expansion of high-entropy materials to high-entropy layered double hydroxide with incorporation of more than 6 cations.

The electrostatic and steric repulsion induced by different superplasticizers on ground granulated blast furnace slag in alkaline media have been studied. The superplasticizers were sulfonated naphthalene, sulfonated melamine, vinyl copolymer, and polycarboxylate- based admixtures. With these superplasticizers the slag suspensions had negative zeta potentials, ranging from -3 to -10 mV. For the first time the adsorbed layer thicknesses for superplasticizers on slag using colloidal probe atomic force microscopy has been measured. To model the interparticle force interactions an effective Hamaker constant was computed from dielectric properties measured on a dense slag sample produced by spark plasma sintering. The obtained results conclude that the dispersion mechanism for all the superplasticizers studied in the present work is mainly dominated by the steric repulsion. Results were then used in a yield stress model, YODEL, to predict the yield stress with and without the superplasticizers. Predictions of the yield stress agreed well with experimental results.