In multiferroic materials, adiabatic temperature changes can be obtained by the combined application of electric, stress, and magnetic fields. These external stimuli provide additional channels of entropy variations resulting in a multi-caloric response. In ferroelectric (FE) materials, caloric responses can be obtained with the application of electric and mechanical fields. Here, we compute the intrinsic elastocaloric and stress–mediated electrocaloric behavior of prototypical FE materials using the Landau–Devonshire theory of phase transformations with appropriate electrical and electro–mechanical boundary conditions. We show that an elastocaloric adiabatic temperature variation of 12.7 °C can be obtained in PbTiO3 with the application of uniaxial tensile stress of 500 MPa near its Curie point. This is 59% higher than its pure intrinsic electrocaloric response for an electric field difference of 100 kV/cm. Moreover, external stresses allow the maximum electro–elastocaloric response to be tuned towards room temperature. Our calculations show that relaxor FEs should exhibit large adiabatic temperature variations in relatively broad temperature ranges. These findings indicate that caloric responses in ferroic materials can be deterministically controlled and enhanced by utilizing a variety of external stimuli.
ZnO nanorods have been studied extensively due to facile synthesis and useful optoelectronic properties for applications in nanoscale devices. In a common two-step procedure, an ethanolic Zn 2+ precursor solution is used to deposit ZnO seed crystals on a substrate, which is then immersed in an aqueous Zn 2+ precursor solution to grow the nanorods. Here, a forced hydrolysis technique was employed based on additions of water and heat to the seed precursor solution before depositing the seeds on commercial fluorine-doped tin oxide (FTO)/glass substrates. ZnO nanorods were then grown from these seeds by chemical bath deposition. Analyses showed that the forced hydrolysis resulted in an increase in seed crystallite size and a decrease in the number of seeds deposited. With increasing seed size, the number density of nanorods decreased, while the length and diameter of each rod increased. These findings offer a simple method for exerting control over the number density of ZnO nanorods that is compatible with the rough FTO surface, unlike other methods that require smoother substrates.R. Riman-contributing editor Manuscript No. 34016.
The dependence of the polarization texture topology in ferroelectric PbTiO3 nanoparticles, embedded in a dielectric matrix, on the particle shape and size was investigated with a time-dependent Landau-Ginzburg-Devonshire approach combined with coupled-physics finite-element-method based simulations. Particle shapes belonging to the superellipsoidal family were probed, including octahedral, cubic, and intermediate geometries. For each shape, a parametric sweep of particle sizes ranging from 2 to 40 nm was conducted, revealing a general trend for the texture transformations from a monodomain, through a vortex-like, to a multidomain state, as the size increases. Critical particle sizes for the texture instabilities were found to be strongly dependent on the particle shape, with octahedral particles undergoing transitions at much larger volumes, compared to the cubic particles. Furthermore, for each of the considered non-spherical shapes of appropriate size, it was possible to obtain multiple vortex-like textures whose paraelectric cores are aligned with every rotational axis of the particle point symmetry group. The shape-dependent metastability of the vortex-like textures opens up new avenues for controlling polarization at the nanoscale in a variety of technological applications.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.