http://sces.phys.utk.edu/mostcited/mc1_1114.pdf

Colossal Magnetoresistant Materials: The Key Role of Phase Separation

A large body of work has been reported in the last 5 years on the development of lead-free piezoceramics in the quest to replace lead–zirconate–titanate (PZT) as the main material for electromechanical devices such as actuators, sensors, and transducers. In specific but narrow application ranges the new materials appear adequate, but are not yet suited to replace PZT on a broader basis. In this paper, general guidelines for the development of lead-free piezoelectric ceramics are presented. Suitable chemical elements are selected first on the basis of cost and toxicity as well as ionic polarizability. Different crystal structures with these elements are then considered based on simple concepts, and a variety of phase diagrams are described with attractive morphotropic phase boundaries, yielding good piezoelectric properties. Finally, lessons from density functional theory are reviewed and used to adjust our understanding based on the simpler concepts. Equipped with these guidelines ranging from atom to phase diagram, the current development stage in lead-free piezoceramics is then critically assessed.

Perspective on the Development of Lead-free Piezoceramics

Ferroelectric, dielectric and piezoelectric properties of ferroelectric thin films and ceramics are reviewed with the aim of providing an insight into different processes which may affect the behaviour of ferroelectric devices, such as ferroelectric memories and micro-electro-mechanical systems. Taking into consideration recent advances in this field, topics such as polarization switching, polarization fatigue, effects of defects, depletion layers, and depolarization fields on hysteresis loop behaviour, and contributions of domain-wall displacement to dielectric and piezoelectric properties are discussed. An introduction into dielectric, pyroelectric, piezoelectric and elastic properties of ferroelectric materials, symmetry considerations, coupling of electro-mechanical and thermal properties, and definitions of relevant ferroelectric phenomena are provided.

https://iopscience.iop.org/article/10.1088/0034-4885/61/9/002/pdf

Ferroelectric, dielectric and piezoelectric properties of ferroelectric thin films and ceramics

In the present review, aerogels designate dried gels with a very high relative pore volume. These are versatile materials that are synthesized in a first step by low-temperature traditional sol-gel chemistry. However, while in the final step most wet gels are often dried by evaporation to produce so-called xerogels, aerogels are dried by other techniques, essentially supercritical drying. As a result, the dry samples keep the very unusual porous texture which they had in the wet stage. In general these dry solids have very low apparent densities, large specific surface areas, and in most cases they exhibit amorphous structures when examined by X-ray diffraction (XRD) methods. In addition, they are metastable from the point of view of their thermodynamic properties. Consequently, they often undertake a structural evolution by chemical transformation, when aged in a liquid medium and/or heat treated. As aerogels combine the properties of being highly divided solids with their metastable character, they can develop very attractive physical and chemical properties not achievable by other means of low temperature soft chemical synthesis. In other words, they form a new class of solids showing sophisticated potentialities for a range of applications. These applications as well as chemical and physical aspects of these materials were regularly detailed and discussed in a series of symposia on aerogels,1-5 the last of them being held in Albuquerque in 2000.6 Reviews were also regularly published, either on both xerogels and aerogels7 or more focused on the applications of aerogels.8-13 The particularly interesting properties of aerogels arise from the extraordinary flexibility of the solgel processing, coupled with original drying techniques. The wet chemistry is not basically different for making xerogels and aerogels. As this common basis has been extensively detailed in recent books,14 it does not need to be reviewed. Compared to traditional xerogels, the originality of aerogels comes from * To whom all correspondence should be addressed. † Institut de Recherches sur la Catalyse. ‡ Laboratoire d’Application de la Chimie à l’Environnement. 4243 Chem. Rev. 2002, 102, 4243−4265

https://is.muni.cz/el/1431/podzim2006/C7780/um/Read/2711172/aerogel_Pajonk_ChRev02_4243.pdf

Chemistry of Aerogels and Their Applications

The present invention provides stretchable, and optionally printable, semiconductors and electronic circuits capable of providing good performance when stretched, compressed, flexed or otherwise deformed. Stretchable semiconductors and electronic circuits of the present invention preferred for some applications are flexible, in addition to being stretchable, and thus are capable of significant elongation, flexing, bending or other deformation along one or more axes. Further, stretchable semiconductors and electronic circuits of the present invention may be adapted to a wide range of device configurations to provide fully flexible electronic and optoelectronic devices.

http://science.sciencemag.org/content/sci/311/5758/208.full.pdf

Stretchable form of single crystal silicon for high performance electronics on rubber substrates

We report the results of an investigation into the grain-size dependence of lattice structure for barium titanate (${\mathrm{BaTiO}}_{3}$) ceramics prepared by a sol-gel method. Raman and infrared spectroscopy, x-ray diffraction, and differential scanning calorimetry were used in combination with electron microscopy to study the evolution of lattice structure and phase transformation behavior with heat treatment and grain growth from the nano scale to the micron scale for ${\mathrm{BaTiO}}_{3}$ polycrystals. Raman spectroscopy and optical second-harmonic-generation measurements indicated the onset of local room-temperature acentric crystal symmetry with heat treatment and crystallite growth, well before the observation of any tetragonal structure by x-ray diffraction. Analysis of the room-temperature Raman spectra for ultrafine grain (grain size 0.1 \ensuremath{\mu}m) polycrystals suggested that a locally orthorhombic structure preceded the globally tetragonal form with grain growth. In support of this observation, differential scanning calorimetry suggested the orthorhombic-tetragonal phase transformation shifts up through room temperature with decreasing grain size. Hot-stage transmission electron microscopy studies revealed that fine grain (grain size \ensuremath{\approxeq}0.1 \ensuremath{\mu}m) ceramics, which showed a thermal anomaly associated with the cubic-tetragonal phase transformation, were untwinned at room temperature, as well as on cycling through the normal Curie temperature, suggesting a single-domain state for individual grains. The findings are discussed in light of a number of possible causes, including the presence of processing-related hydroxyl defects and the effect of elastic constraints on phase transformation behavior for ${\mathrm{BaTiO}}_{3}$ grains in a polycrystalline microstructure. \textcopyright{} 1996 The American Physical Society.

Grain-size effect on structure and phase transformations for barium titanate

We report the effect of interfaces (and thus internal surface area effects) on the value of dielectric constant (K′) calculated from capacitance and geometry data for sub-micron barium titanate (BaTiO3) ceramics prepared with decreasing grain size (and grain volumes). A series model is proposed to explain the decreasing values of apparent K′ obtained for grain sizes below 0.5 μm. A distinction is made between the true dielectric constant (K′) and the apparent dielectric constant (K′) calculated from experimental data. The progressive suppression in K′ is explained in terms of ferroelectric grains of constant dielectric constant (K′1) separated by a lower-K 2 boundary region (i.e., grain boundary) of constant thickness (d 2). The problem is one of an increasing interfacial surface area to grain volume ratio in fine-grain dielectrics. We begin by reporting original dielectric data for high pressure-densified ultrafine-grain BaTiO3 ceramics. Chemically prepared BaTiO3 powder was consolidated at high...

The role of interfaces on an apparent grain size effect on the dielectric properties for ferroelectric barium titanate ceramics

A technique for creating patterns of material deposited on a surface involves forming a self-assembled monolayer in a pattern on the surface and depositing, via chemical vapor deposition or via sol-gel processing, a material on the surface in a pattern complementary to the self-assembled monolayer pattern. The material can be a metal, metal oxide, or the like. The surface can be contoured, including trenches or holes, the trenches or holes remaining free of self-assembled monolayer while the remainder of the surface is coated. When exposed to deposition conditions, metal or metal oxide is deposited in the trenches or holes, and remaining portions of the article surface remain free of deposition. The technique finds particular use in creation of conductive metal pathways selectively within holes passing from one side of a substrate to another.

Self-assembled monolayer directed patterning of surfaces

When an electric field is applied to a dielectric material under adiabatic conditions there is a resultant change in temperature, a phenomenon known as the electrocaloric effect Compositions in the Pb(Zr,Sn,Ti)O3 system (PZST) have several phases of nearly equal free energy, allowing antiferroelectric (AFE) to ferroelectric (FE) and paraelectric (PE) to ferroelectric (FE) transitions to occur Data are presented for electrocaloric measurements on AFE materials in the vicinity of the Curie point The effect of microstructure is reported, and experimental values are related to dielectric properties through thermodynamic relations Culmination of this work resulted in the largest electrocaloric effect (26°K) measured to date for coarse grain material in the PZST system

The effects of microstructure on the electrocaloric properties of Pb(Zr,Sn,Ti)O3 ceramics

This paper reports on infrared spectroscopy that was used to monitor and characterize solutions used in the preparation of PZT 53/47 powders, dried gels, and thin layers deposited on platinized silicon substrates. It was found that careful control of the chemistry of the precursor solutions, in particular the control of the formation of esters and their elimination, resulted in reproducible solutions which could be used to prepare thin layers with superior properties. In addition, it was found that phase development and microstructure were related to the precursor chemistry. Single-phase perovskite layers with uniform microstructures resulted from ester-free solutions and were suitable for ferroelectric applications (P[sub r] [approximately] 22 [mu]C/cm[sup 2], E[sub c] [approximately] 80 kV/cm, K [approximately] 800, tan [delta] [approximately] 0.01).

David A. Payne

Papers

Grain-size effect on structure and phase transformations for barium titanate

The role of interfaces on an apparent grain size effect on the dielectric properties for ferroelectric barium titanate ceramics

Self-assembled monolayer directed patterning of surfaces

The effects of microstructure on the electrocaloric properties of Pb(Zr,Sn,Ti)O3 ceramics

Processing Effects in the Sol–Gel Preparation of PZT Dried Gels, Powders, and Ferroelectric Thin Layers